-
Health Sciences
Neurology (clinical)
-
Health Sciences
Medicine (miscellaneous)
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Neurology
-
Life Sciences
Neuroscience (miscellaneous)
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Genetics
-
Health Sciences
Psychiatry and Mental Health
-
Life Sciences
Genetics
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Genetics
-
Health Sciences
Neurology (clinical)
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Genetics
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Neurology
-
Health Sciences
Medicine (miscellaneous)
-
Health Sciences
Genetics (clinical)
-
Life Sciences
Neurology
-
Life Sciences
Genetics
-
Life Sciences
Genetics
-
Life Sciences
Genetics
-
Life Sciences
Neurology
-
Health Sciences
Pediatrics, Perinatology and Child Health
-
Health Sciences
Neurology (clinical)
-
Health Sciences
Medicine (miscellaneous)
-
Social Sciences & Humanities
Psychology (miscellaneous)
-
Health Sciences
Psychiatry and Mental Health
-
Life Sciences
Genetics
-
Social Sciences & Humanities
Education
-
Health Sciences
Genetics (clinical)
-
Health Sciences
Medicine (miscellaneous)
-
Life Sciences
Genetics
-
Life Sciences
Neurology
-
Life Sciences
Neurology
-
Life Sciences
Genetics
-
Health Sciences
Pharmacology (medical)
-
Life Sciences
Neuroscience (miscellaneous)
-
Health Sciences
Medicine (miscellaneous)
-
Health Sciences
Neurology (clinical)
-
Life Sciences
Neurology
Carmen Silvia Molleis Galego MIZIARA; Maria Luiza Giraldes De MANREZA; Leticia Lessa MANSUR; Umbertina Conti REED; Laura Maria De Figueiredo Ferreira GUILHOTO et al.
2012.
Impact of benign childhood epilepsy with centrotemporal spikes (bects) on school performance.
Seizure (london; england).
21,
87-91.
-
Life Sciences
Neurology
Elaine Cristina Da SILVA; Darlene Lessa MACHADO; Maria Bernadete Dutra RESENDE; Renata F SILVA; Edmar ZANOTELI et al.
2012.
Motor function measure scale; steroid therapy and patients with duchenne muscular dystrophy.
Arquivos de neuro-psiquiatria (impresso).
70,
191-195.
-
Life Sciences
Clinical Biochemistry
-
Social Sciences & Humanities
Education
Luiz Alberto BACHESCHI; Mario Augusto TARICCO; Umbertina Conti REED.
2012.
Professor luiz alcides manreza.
Arquivos de neuro-psiquiatria (impresso).
70,
477-477.
-
Health Sciences
Pediatrics, Perinatology and Child Health
Felippe BORLOT; M L SANTOS; M BANDEIRA; P B LIBERALESSO; Fernando KOK et al.
2012.
Anti-n-methyl d-aspartate receptor encephalitis in childhood.
Jornal de pediatria (impresso).
88,
275-278.
-
Life Sciences
Parasitology
-
Health Sciences
Psychiatry and Mental Health
Guilherme Vanoni POLANCZYK; Erasmo Barbante CASELLA; Eurípedes Constantino MIGUEL; Umbertina Conti REED.
2012.
Attention deficit disorder/hyperactivity: a scientific overview.
Clinics.
67,
1125-1126.
-
Health Sciences
Cardiology and Cardiovascular Medicine
-
Health Sciences
Neurology (clinical)
-
Health Sciences
Pediatrics, Perinatology and Child Health
Valdecir Antonio SIMON; Maria Bernadete Dutra RESENDE; Margarete Andreozzi Vaz Pereira SIMON; Edmar ZANOTELI; Umbertina Conti REED.
2011.
Duchenne muscular dystrophy. quality of life among 95 patients evaluated using the life satisfaction index for adolescents.
Arquivos de neuro-psiquiatria (impresso).
69,
19-22.
-
Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Ana F B FERREIRA; Mary Souza De CARVALHO; Maria Bernadete Dutra RESENDE; Alda WAKAMATSU; Umbertina Conti REED et al.
2011.
Phenotypic and immunohistochemical characterization of sarcoglycanopathies.
Clinics (usp. impresso).
66,
1713-1719.
-
Health Sciences
Medicine (miscellaneous)
Rui Zhu ZHANG; Yaqun ZOU; Te Cheng PAN; Dessislava MARKOVA; Andrzej FERTALA et al.
2010.
Recessive col6a2 c-globular missense mutations in ullrich congenital muscular dystrophy: role of the c2a splice variant.
Journal of biological chemistry (online).
285,
10005-100015.
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Health Sciences
Psychiatry and Mental Health
Cristiana BOLFER; Erasmo Barbante CASELLA; Marcus Vinícius Chrysóstomo BALDO; Amanda Manzini MOTA; Miriam Harumi TSUNEMI et al.
2010.
Reaction time assessment in children with adhd.
Arquivos de neuro-psiquiatria (impresso).
68,
282-286.
-
Life Sciences
Neurology
Edmar ZANOTELI; Jessica Ruivo MAXIMINO; Umbertina Conti REED; Gerson CHADI.
2010.
Spinal muscular atrophy: from animal model to clinical trial.
Functional neurology (roma. testo stampato).
25,
73-79.
-
Health Sciences
Neurology (clinical)
Samara Lamounier Santana PARREIRA; Maria Bernadete Dutra RESENDE; Edmar ZANOTELI; Mary Souza De CARVALHO; Suely Kazue Nagahashi MARIE et al.
2010.
Comparison of motor strenght and function in patients with duchenne muscular dystrophy with or without steroid therapy.
Arquivos de neuro-psiquiatria (impresso).
68,
683-688.
-
Health Sciences
Medicine (miscellaneous)
-
Health Sciences
Medicine (miscellaneous)
Rosana Souza Cardoso ALVES; Maria Bernadete Dutra RESENDE; Robert P SKOMRO; Fabio J F B SOUZA; Umbertina Conti REED.
2009.
Sleep and neuromuscular disorders in children.
Sleep medicine reviews.
13,
133-148.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED.
2009.
Congenital muscular dystrophy. parte i: a review of phenotypical and diagnostic aspects.
Arquivos de neuro-psiquiatria.
67,
144-168.
-
Life Sciences
Biochemistry, Genetics and Molecular Biology (miscellaneous)
Patricia De Campos PIERI; Jeronimo De Alencar NOGUEIRA; Maria Joaquina Marques DIAS; Maria Bernadete Dutra RESENDE; Chong Ae KIM et al.
2009.
A duplex allele-specific amplification pcr to detect smn1 deletion.
Genetic testing and molecular biomarkers (print).
13,
205-208.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED.
2009.
Congenital muscular dystrophy. part ii: a review of pathogenesis and therapeutic perspectives.
Arquivos de neuro-psiquiatria.
67,
343-362.
-
Health Sciences
Medicine (miscellaneous)
Felippe BORLOT; Matheus Schmidt SOARES; Adriana Ávila De ESPÍNDOLA; Umbertina Conti REED; Hamilton MATUSHITA et al.
2009.
Intramedullary spinal teratoma. a rare condition with a good outcome.
Arquivos de neuro-psiquiatria (impresso).
67,
733-735.
-
Health Sciences
Radiology, Nuclear Medicine and Imaging
Maria Concepcion Garcia OTADUY; Claudia Da Costa LEITE; Lidia Mayumi NAGAE; Marco Da Cunha PINHO; Clarissa BUENO et al.
2009.
Further diffusion tensor imaging contribution in horizontal gaze palsy and progerssive scoliosis.
Arquivos de neuro-psiquiatria (impresso).
67,
1054-1056.
-
Life Sciences
Neuroscience (miscellaneous)
Mariana Vieira De Melo Da FONTE; Raquel Portugal Guimarães AMARAL; Maria Olivia Rodrigues COSTA; Maria Concepcion Garcia OTADUY; Leandro T LUCATO et al.
2008.
Meduloblastoma: correlação entre ressonâncoa magnética convencional; difusão e espectroscopia de prótons.
Radiologia brasileira.
41,
373-378.
-
Health Sciences
Medicine (miscellaneous)
Karina TAKATA; Emerson L GASPARETTO; Claudia Costa LEITE; Leandro T LUCATO; Umbertina Conti REED et al.
2007.
Subependymal giant cell astrocytoma in patients with tuberous sclerosis: magnetic resonance imaging findings in ten cases.
Arquivos de neuro-psiquiatria.
65,
313-316.
-
Health Sciences
Medicine (miscellaneous)
Adriana Avila De ESPÍNDOLA; Hamilton MATUSHITA; J M PIMENTA; A C FERNANDES; Sérgio ROSEMBERG et al.
2007.
Brain tumors in the first three years of life: a review of twenty cases.
Arquivos de neuro-psiquiatria.
65,
960-964.
-
Health Sciences
Medicine (miscellaneous)
S L PEREIRA; Maria Bernadete Dutra RESENDE; Marilia D C PEDUTO; Suely Kazue Nagahahsi MARIE; Leandro T LUCATO et al.
2007.
Quantification of muscle strength and motor ability in patients with duchenne muscular dystrophy on steroid therapy.
Arquivos de neuro-psiquiatria.
65,
245-250.
-
Health Sciences
Cardiology and Cardiovascular Medicine
Claudia Costa LEITE; Umbertina Conti REED; M C G OTADUY; M T C LACERDA; M O R COSTA et al.
2005.
Congenital muscular dystrophy with merosin deficiency: 1h mr spectroscopy and diffusion-weighted mr imaging.
Radiology.
235,
(1)
190-196.
-
Health Sciences
Genetics (clinical)
C O VASQUES; Rosa Maria Figueiredo VALÉRIO; Umbertina Conti REED; Rosi Mary GROSSMANN; Fernando KOK.
2005.
Pitfalls in the clinical and electroencephalographic diagnosis of ceroid lipofuscinosis.
Arquivos de neuro-psiquiatria.
Brasil.
63,
(1)
93-96.
-
Life Sciences
Physiology
Carvalho CRF; A C LUNARDI; C C BERTO; Marco ROJO; Maria Bernadete Dutra De RESENDE et al.
2005.
Evolution of pulmonary function in children with duchenne muscular dystrophy: implication of expiratory muscles.
European respiratory journal.
Brasil.
26,
(suppl 49)
499s-499s.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; L G FERREIRA; E C LIU; Resende MBD; Mary Souza De CARVALHO et al.
2005.
Ulrich congenital muscular dystropy and bethlem myopathy: clinical and genetic heterogeneity.
Arquivos de neuro-psiquiatria.
Brasil.
63,
(3-B)
785-790.
-
Life Sciences
Neurology
Ferreira LG; Suely Kazue Nagahashi MARIE; E C LIU; Resende MBD; Mary Souza De CARVALHO et al.
2005.
Dystrophin-gllycoproteins associated in congenital muscular dystropy: immunohistochenical analysis of 59 brazilian cases.
Arquivos de neuro-psiquiatria.
Brasil.
63,
(3-B)
791-800.
-
Health Sciences
Neurology (clinical)
Leite CC; Lucato LT; Martin MGM; Ferreira LG; Resende MBD et al.
2005.
Merosin-deficient congenital muscular dystrophy (cmd): a study of 25 brazilian patients using mri.
Pediatric radiology.
Estados Unidos.
35,
(6)
572-579.
-
Health Sciences
Radiology, Nuclear Medicine and Imaging
Bachin GH; Basso PS; Costa MOR; Otaduy MCG; Lacerda MTC et al.
2004.
Análise 3d dos tumors da fossa posterior por ressonância magnética.
Imagens (campinas).
Brasil.
26,
(4)
273-277.
-
Life Sciences
Neurology
Umbertina Conti REED; Lucio Gobbo FERREIRA; Resende MGD; Mary Souza De CARVALHO; Milberto SCAFF et al.
2004.
Congenital muscular dystrophy with ullrich phenotype: clínical and genetic heterogeneity.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl 2)
87-PO112.
-
Health Sciences
Cardiology and Cardiovascular Medicine
Carvalho CRF; Lunardi AC; Resende MBD; Mary Souza De CARVALHO; Umbertina Conti REED et al.
2004.
Lung function and respiratory muscular evaluation in patients with duchenne muscle dystrophy.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl 2)
87-PO119.
-
Health Sciences
Neurology (clinical)
D P OLIVEIRA; Fernando KOK; L P BALZAN; Pessoa A; Amorim S et al.
2004.
Horizontal gaze palsy with progressive scoliosis: clínical and neuroimag aspects.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl 2)
94-PO146.
-
Health Sciences
Neurology (clinical)
Fernnado KOK; Pessoa A; Pinto LF; Amorim S; Umbertina Conti REED.
2004.
Two siblings with silver hair; hypopigmentation; mental retardation and epilepsy: elejalde syndrome.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl.2)
97-PO154.
-
Life Sciences
Neurology
Amorim S; Oyamada MK; Broto MLI; Umbertina Conti REED; Fernnado KOK.
2004.
Spastic paraplegia; optic atrophy; mental deficiency and axonal neuropathy in two siblings.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl. 2)
112-PO205.
-
Health Sciences
Pediatrics, Perinatology and Child Health
Fernando KOK; Luciana Peterson BALZAN; Simone Consuelo De AMORIM; M FUNAYAMA; A LOTERIO et al.
2004.
Ataxia and vitamin e deficiency in three siblings.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl. 2)
178-PO417.
-
Life Sciences
Neurology
Bueno C; Alho EJL; Pessoa A; Fernnado KOK; Umbertina Conti REED.
2004.
Mobius syndrome associated to axonal neuropathy and hemi-hypertrophy.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl.2)
179-PO421.
-
Health Sciences
Medicine (miscellaneous)
E D CAMPOS; S M Oba SHINJO; Umbertina Conti REED; Resende MBD; M S CARVALHO et al.
2004.
Deletions of study of dystrophyn gene in duchenne and becker muscular dystrophy.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(Supl. 2)
255-PO682.
-
Health Sciences
Medicine (miscellaneous)
Rubens Nelson A A REIMÃO; P S Gerritsen PLAGGERT; Adda C; Matsuhita H; Umbertina Conti REED.
2004.
Frontal foramina; chiari ii malformation and hydrocephalus: case report and developmental issues.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(Supl.2)
265-PO717.
-
Health Sciences
Medicine (miscellaneous)
Rubens Nelson A A REIMÃO; Beatriz LEFÈVRE; Adda C; Matsuhita H; Amorim S et al.
2004.
Grade iii bilateral thalamic glioma in childhood.
Arquivos de neuro-psiquiatria.
Brasil.
62,
(supl. 2)
270-PO733.
-
Health Sciences
Medicine (miscellaneous)
Resende MBD; Lunardi AC; Nakayama A; Simono CM; Nogueira L et al.
2004.
Yoga breathing exercises improve the respiratory function in duchenne dystrophy.
Neuromuscular disorders.
Estados Unidos.
14,
-.
-
Life Sciences
Neurology
Erasmo Barbante CASELLA; Lucio Gobbo FERREIRA; Umbertina Conti REED.
2004.
Episodic somnolence as an unusual early manifestation in an infanto with riley-day syndrome.
Neuromuscular disorders.
Estados Unidos.
14,
(8-9)
572-.
-
Health Sciences
Veterinary (miscellaneous)
Juliana Gurgel GIANNETTI; Umbertina Conti REED; Suely Kazue Nagahahsi MARIE; Edmar ZANOTELLI; M A T FIREMAN et al.
2003.
Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.
Journal of child neurology.
Estados Unidos.
18,
(3)
235-240.
-
Health Sciences
Neurology (clinical)
Rubens Nelson A A REIMÃO; P S Gerritsen PLAGGERT; Carla Cristina ADDA; Hamilton MATUSHITA; Umbertina Conti REED.
2003.
Frontal foramina; chiari ii malformation; and hydrocephalus in a female.
Pediatric neurology.
Estados Unidos.
29,
(4)
341-344.
-
Health Sciences
Medicine (miscellaneous)
Rubens Nelson Amaral De Assis REIMÃO; P S Gerritsen PLAGGERT; Carla Cristina ADDA; Hamilton MATUSHITA; Umbertina Conti REED.
2003.
Frontal foramina; bone growth and chiari ii.
Journal of the neurological sciences.
Estados Unidos.
214,
(1-2)
79-79.
-
Health Sciences
Medicine (miscellaneous)
P S Gerritsen PLAGGERT; Chong Ae KIM; Maria Joaquina Marques DIAS; Umbertina Conti REED; Fernando KOK et al.
2002.
Encefalocele occipital como principal manifestação da síndrome das bridas amnióticas: relato de caso.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
98-98.
-
Health Sciences
Radiology, Nuclear Medicine and Imaging
A M M OLIVEIRA; M C H OTADUY; Claudia Costa LEITE; M T C LACERDA; Fernando KOK et al.
2002.
Anormalidades da espectroscopia por ressonância magnética na síndrome de sjögren-larsson.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
96-96.
-
Health Sciences
Medicine (miscellaneous)
P S Gerritsen PLAGGERT; Lídia Mayume Nagae POETSCHER; A M M OLIVEIRA; Fernando KOK; M T C LACERDA et al.
2002.
Nova forma de leucodistrofia com calcificações intracranianas e cisto hipertensivo de tronco cerebral.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
96-96.
-
Social Sciences & Humanities
Psychology (miscellaneous)
Fernando KOK; Umbertina Conti REED; Maria Rita Passos BUENO; M L MARTYN; O SUZUKI et al.
2002.
Estudo clínico e molecular de uma familia com três afetados pela síndrome de knobloch (encefalocele occipital e degeneração vitreoretiniana).
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
96-96.
-
Health Sciences
Medicine (miscellaneous)
Fernando KOK; M C M SILVA; M L MARTYN; A M M OLIVEIRA; Mario Wilson Iervolino BROTTO et al.
2002.
Eletroneuromiografia com descargas miotônicas na ataxia com apraxia oculomotora (aoa1). um achado atípico?.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
95-95.
-
Health Sciences
Medicine (miscellaneous)
A M M OLIVEIRA; Fernando KOK; Umbertina Conti REED; Chong Ae KIM; Hamilton MATUSHITA et al.
2002.
Síndrome de russel. apresentação clássica e atípica: relato de 2 casos.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
151-151.
-
Health Sciences
Neurology (clinical)
E C LIU; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Milberto SCAFF; Mary Souza CARVALHO et al.
2002.
Hipotonia congênita de causa neuromuscular: revisão de 160 casos.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
188-188.
-
Health Sciences
Medicine (miscellaneous)
A M M OLIVEIRA; Umbertina Conti REED; Livia Cunha ELKIS; Maria Luiza Giraldes De MANREZA; D H NAKANISHI et al.
2002.
Discinesia paroxística cinesiogênica: diagnóstico diferencial de pseudocrises.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
210-210.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Maria Bernadete Dutra RESENDE; Lucio Gobbo FERREIRA; Mary Souza CARVALHO; Aron DIAMENT et al.
2002.
King-denborough syndrome. report of two brazilian cases.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(3-B)
739-741.
-
Life Sciences
Neuroscience (miscellaneous)
Umbertina Conti REED; Rubens Nelson A A REIMÃO; Adriana Ávila De ESPÍNDOLA; Fernando KOK; Lucio Ferreira GOBBO et al.
2002.
Schwartz-jampel syndrome. report of five cases.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(3-B)
734-738.
-
Life Sciences
Genetics
L Silveira MORIYANA; A Silveira MORIYAMA; Suely Kazue Nagahahsi MARIE; T Silveira MORIYAMA; Mary Souza CARVALHO et al.
2002.
Avaliação da musculatura de panturrilhas de pacientes com distrofia muscular de duchenne através de ressonância magnética nuclear magnética.
Arquivos de neuro-psiquiatria.
Brasil.
60,
(suppl. 1)
134-134.
-
Life Sciences
Genetics
Juliana Gurgel GIANNETTI; Marta CANOVAS; M L BANG; Umbertina Conti REED; Suely Kazue Nagahashi MARIE et al.
2002.
The lack of the c-terminal domain of nebulin in a patient with nemaline myopathy.
Muscle & nerve.
Estados Unidos.
25,
(5)
747-752.
-
Health Sciences
Medicine (miscellaneous)
Juliana Gurgel GIANETTI; Umbertina Conti REED; Edmar ZANOTELLI; Lineu César WERNECK; A H BEGGS et al.
2002.
Diferenças no padrão de distribuição dos rods e na proporção de tipo de fibras com a evolução da miopatia nemalínica.
O dendrito.
Brasil.
8,
(1)
5-5.
-
Life Sciences
Physiology
Juliana Gurgel GIANNETTI; Umbertina Conti REED; Edmar ZANOTELLI; Lineu César WERNECK; A H BEGGS et al.
2002.
Rod distribution and muscle fibers type modification in the progression of nemaline myopathy.
Neuromuscular disorders.
Inglaterra.
12,
(7/8)
766-766.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED.
2002.
Doenças neuromusculares.
Jornal de pediatria.
Brasil.
78,
(suppl. 1)
S89-S103.
-
Life Sciences
Genetics
Juliana Gurgel GIANNETTI; M L BANG; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mayana ZATZ et al.
2002.
Lack of the c-terminal domain of nebulin in a patient with nemaline myopathy.
Muscle & nerve.
Estados Unidos.
25,
747-752.
-
Health Sciences
Radiology, Nuclear Medicine and Imaging
Cláudia Da Costa LEITE; Umbertina Conti REED; M G OTADUY; M T C LACERDA; M O R COSTA et al.
2002.
Proton magnetic resonance spectroscopy (1h-mrs) and diffusion-weighted images (dw) in congenital muscular dystrophy with merosin deficiency.
Radiology.
Estados Unidos.
225,
132-.
-
Life Sciences
Genetics
M T C LACERDA; M O R COSTA; Fernando KOK; C O VASQUES; Sérgio ROSEMBERG et al.
2002.
The involvement of optic system x-linked adrenoleucodystrophy: assessment of 24 cases.
Journal of neuroradiology.
França.
29,
(1S)
223-.
-
Health Sciences
Radiology, Nuclear Medicine and Imaging
Cláudia Da Costa LEITE; Umbertina Conti REED; M G OTADUY; M T C LACERDA; M O R COSTA et al.
2002.
Congenital muscular dystrophy (cmd) with laminin alpha 2 deficiency: proton magnetic resonance spectroscopy (1 hmrs) and diffusion-weighted images (dw).
Journal of neuroradiology.
França.
29,
(1S)
154-.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Juliana Gurgel GIANNETTI; Maria Bernadete Dutra De RESENDE; L G FERREIRA; M S CARVALHO et al.
2002.
Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases.
Neuromuscular disorders.
Inglaterra.
12,
(7/8)
744-.
-
Health Sciences
Cardiology and Cardiovascular Medicine
Umbertina Conti REED; Maria Bernadete Dutra De RESENDE; L G FERREIRA; M S CARVALHO; A WAKAMATSU et al.
2002.
Congenital minimal changes myopathy: clinical adn immunohistochemical study.
Neuromuscular disorders.
Inglaterra.
12,
(7/8)
758-.
-
Health Sciences
Neurology (clinical)
Cláudia Da Costa LEITE; M T C LACERDA; M O R COSTA; M G OTADUY; L G FERREIRA et al.
2002.
Merosin-deficient congenital muscular dystrophy: lack of specificity of proton magnetic resonance spectoscopy associated to mri in eith patients.
Brain & development.
Estados Unidos.
24,
-.
-
Health Sciences
Neurology (clinical)
H Vand Der Linden JUNIOR; Maria Bernadete Dutra De RESENDE; L G FERREIRA; M S CARVALHO; Suely Kazue Nagahashi MARIE et al.
2002.
Congenital muscular dystrophy. report of two atypical cases.
Brain & development.
Estados Unidos.
24,
643-.
-
Health Sciences
Neurology (clinical)
M S T SOUZA; Fernando KOK; Cláudia Da Costa LEITE; M T C LACERDA; M O R COSTA et al.
2002.
Leucoencephalopaty with vanishing white matter: report of five brazilian cases.
Brain & development.
Estados Unidos.
24,
576-.
-
Health Sciences
Neurology (clinical)
A A ESPINDOLA; Hamilton MATUSHITA; Aron Judka DIAMENT; Umbertina Conti REED.
2002.
Brain tumors in children. a review of 84 brazilian cases.
Brain & development.
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Health Sciences
Medicine (miscellaneous)
Juliana Gurgel GIANNETTI; Umbertina Conti REED; M BANG; K PELIN; K DONNER et al.
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Nebulin expression in patients with nemaline myopathy.
Neuromuscular disorders.
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Umbertina Conti REED.
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Distrofia muscular congênita.
Arquivos de neuro-psiquiatria.
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59,
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Health Sciences
Neurology (clinical)
Maria Bernadete Dutra De RESENDE; Umbertina Conti REED; Adriana Avila De ESPÍNDOLA; Lúcio Gobbo FERREIRA; Mary Souza CARVALHO et al.
2001.
Deflazacort in duchenne muscular dystrophy: preliminary results in a brazilian series.
Neuromuscular disorders.
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Health Sciences
Genetics (clinical)
Juliana Gurgel GIANNETTI; Marta CANOVAS; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mayana ZATZ et al.
2001.
The lack of the c-terminal domain of nebulin in a patient with nemaline myopathy.
Neuromuscular disorders.
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Social Sciences & Humanities
Psychology (miscellaneous)
Adriana Ávila De ESPÍNDOLA; Umbertina Conti REED; Fernando KOK; Lucio Gobbo FERREIRA; Maria Bernadete Dutra RESENDE et al.
2000.
Síndrome de schwartz-jampel: relato de 4 casos.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
73-73.
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Health Sciences
Medicine (miscellaneous)
Cleurecy Oliveira VASQUES; Thelma Regina Correia MESSIAS; Umbertina Conti REED; Fernando KOK; Aron J DIAMENT.
2000.
Hematoma subdural crônico em pacientes com doença de menkes.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
123-123.
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Life Sciences
Neurology
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Lucio Gobbo FERREIRA; Maria Bernadete Dutra RESENDE; Mary Souza De CARVALHO et al.
2000.
Congenital muscular dystrophy (cmd): a study of neuroimaging findings in 25 merosin-deficiency brazilian cases.
Neuromuscul disord.
Inglaterra.
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380-380.
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Health Sciences
Neurology (clinical)
Umbertina Conti REED; Lucio Gobbo FERREIRA; Mariz VAINZOF; Maria Bernadete Dutra RESENDE; Mary Souza De CARVALHO et al.
2000.
Congenital muscular dystrophy (cmd): clinical immunohistochemical correlation in a brazilian casuistic: 40 cases.
Neuromuscular disorders.
Inglaterra.
10,
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381-381.
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Life Sciences
Neurology
Adriana Avila De ESPÍNDOLA; Umbertina Conti REED; Maria Bernadete Dutra De RESENDE; Aron J DIAMENT; Milberto SCAFF et al.
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Congenital muscular dystrophy (cmd): histopathological aspects in a brazilian casuistic of 55 cases.
Neuromuscul disord.
Inglaterra.
10,
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Health Sciences
Pediatrics, Perinatology and Child Health
Lucio Gobbo FERREIRA; Umbertina Conti REED; Mary Souza De CARVALHO; Maria Bernadete Dutra De RESENDE; Aron J DIAMENT et al.
2000.
Doença de pompe forma de adulto. dificuldades diagnósticas.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
75-75.
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Health Sciences
Neurology (clinical)
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mariz VAINZOF; Lucio Gobbo FERREIRA; Juliana Gurgel GIANNETTI et al.
2000.
Heterogeniety of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases.
Journal of child neurology.
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15,
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172-178.
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Health Sciences
Medicine (miscellaneous)
Maria Bernadete Dutra RESENDE; Umbertina Conti REED; Mary Souza De CARVALHO; Lucio Gobbo FERREIRA; Aron J DIAMENT et al.
2000.
Importância da expressão das isoformas maturativas da miosina em miopatia por alterações mínimas.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
69-69.
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Health Sciences
Pediatrics, Perinatology and Child Health
Umbertina Conti REED; Lucio Gobbo FERREIRA; Maria Bernadete Dutra De RESENDE; Mary Souza De CARVALHO; Aron J DIAMENT et al.
2000.
Merosin-positive congenital muscular dystrophy: a clinical-immunohistochemical study of nine patients with severe phenotype.
Neuromuscular disord.
Brasil.
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380-380.
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Life Sciences
Neuroscience (miscellaneous)
Mary Souza De CARVALHO; Fabiana Cristina LUIZ; Maria Angela Amaral Gurgel VIANNA; A M E SALLUM; Maria Bernadete Dutra De RESENDE et al.
2000.
Miosite por corpos de inclusão: estudo imunohistoquímico dos antígenos de histocompatibilidade maior; moléculas de adesão de fenotipagem das células inflamatórias.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
67-67.
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Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; A S FERNANDES; Maria Joaquina Marques DIAS; Sérgio ROSEMBERG; Umbertina Conti REED et al.
2000.
The relevance of muscle histochemical alterations and mitochondrial dna mutation in leigh´s syndrome in brazilian casuistics.
Neuromuscular disorders.
Inglaterra.
10,
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346-346.
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Health Sciences
Genetics (clinical)
Kelly Cristina MOUTINHO; A M E SALLUM; Maria Angela Amaral Gurgel VIANNA; Mary Souza De CARVALHO; Lucio Gobbo FERREIRA et al.
2000.
Dermatomiosite juvenil: correlação do complexo de ataque à membrana com atrofia perifascicular e duração clínica.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
76-76.
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Health Sciences
Pediatrics, Perinatology and Child Health
Dilza Roéga COELHO; Thelma Regina Correia MESSIAS; Celia P KOIFFMANN; Cintia FRIDMAN; Mario Wilson Iervolino BROTTO et al.
2000.
Eletroneuromiografia com padrão miopático em lactentes com síndrome de prader-willi.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
71-71.
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Health Sciences
Medicine (miscellaneous)
Juliana Gurgel GIANNETTI; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Moacir A T FIREMAN et al.
2000.
Estudo imunohistoquímico de proteínas musculares na miopatia nemalínica.
Arquivos de neuro-psiquiatria.
Brasil.
58,
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65-65.
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Life Sciences
Neurology
Juliana Gurgel GIANNETTI; Umbertina Conti REED; Marie Louise BANG; Katarina PELIN; Kati DONNER et al.
2000.
Expressão da nebulina em pacientes com miopatia nemalínica.
Arquivos de neuro-psiquiatria.
Brasil.
58,
(supl. II)
69-69.
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Health Sciences
Neurology (clinical)
A M E SALLUM; M YOKOO; Maria Bernadete Dutra RESENDE; Lucio Gobbo FERREIRA; Umbertina Conti REED et al.
2000.
Mhc class 1 as an additional marker to the course of juvenile dermatomyositis.
Neuromuscular disorders.
Inglaterra.
10,
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358-358.
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Life Sciences
Genetics
Sérgio Augusto FERNANDES; José Albino Da PAZ; Maria Joaquina Marques DIAS; Sérgio ROSEMBERG; Fernando KOK et al.
2000.
Pesquisa de mutações no gene atpase6 do dna mitocondrial na síndrome de leigh.
Arquivos de neuro-psiquiatria.
Brasil.
58,
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98-98.
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Health Sciences
Neurology (clinical)
Umbertina Conti REED.
2000.
Congenital muscular dystrophy: a study phenotypical variability and clinical-immunohistochemical correlation.
Arquivos de neuro-psiquiatria.
Brasil.
58,
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589-590.
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Health Sciences
Pediatrics, Perinatology and Child Health
Umbertina Conti REED; Lucio Gobbo FERREIRA; Resende MBD; Mary Souza De CARVALHO; Aron J DIAMENT et al.
2000.
Merosin-positive congenital muscular dystrophy (cmd): report of a case with marked reduction of â1 laminin chain immunoreactivity.
Neuromusc disord.
África Do Sul.
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381-.
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Health Sciences
Pediatrics, Perinatology and Child Health
Umbertina Conti REED; Lucio Gobbo FERREIRA; Mariz VAINZOF; Mary Souza De CARVALHO; Resende MBD et al.
1999.
Analise estatística comparativa dos aspectos clínicos; histopatológicas e imunohistoquimicos de pacientes com distrofia muscular congênita merosina-positiva e merosina-negativa.
Anais do xii jornada brasileira de doenças neuromusculares.
Brasil.
(PO.04)
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Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Lucio Gobbo FERREIRA; Mariz VAINZOF; Mary Souza De CARVALHO; Resende MBD et al.
1999.
Distrofia muscular congênita com déficit parcial de merosina: aspectos clínicos; histopatológicos e imunohistoquimicos.
Anais da xii jornada brasileira de doenças neuromusculares.
Brasil.
(PO-05)
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Health Sciences
Neurology (clinical)
Umbertina Conti REED; Lucio Gobbo FERREIRA; Lívia Cunha ELKIS; Mary Souza De CARVALHO; Suely Kazue Nagahashi MARIE et al.
1999.
Síndrome de walker-warburg.
Anais da xii jornada brasileira de doenças neuromusculares.
Brasil.
(PO.06)
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Health Sciences
Medicine (miscellaneous)
Resende MBD; Umbertina Conti REED; Mary Souza De CARVALHO; Lucio Gobbo FERREIRA; Aron J DIAMENT et al.
1999.
Miopatia congênita com alterações mínimas: aspectos clínicos e morfológicos.
Anais da xii jornada brasileira de doenças neuromusculares.
Brasil.
(PO.09)
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Health Sciences
General Medicine
Suely Kazue Nagahashi MARIE; Takeuchi C; Sirevenga V; Mary Souza De CARVALHO; Lucio Gobbo FERREIRA et al.
1999.
Miopatia por acúmulo de lípides por defeito de oxidação dos ácidos graxos.
Anais da xii jornada brasileira de doenças neuromusculares.
Brasil.
(PO.14)
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Health Sciences
Pediatrics, Perinatology and Child Health
Umbertina Conti REED; Ana Maria Clous TSANACLIS; Mariz VAINZOF; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO et al.
1999.
Merosin-positive congenital muscular dystrophy in two siblings with cataracts and slight mental retardation.
Brain & development.
Japão.
21,
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274-278.
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Health Sciences
Rheumatology
Umbertina Conti REED; Maria Bernadete Dutra RESENDE; Mary Souza De CARVALHO; Laura Maria De Figueiredo Ferreira GUILHOTO; Aron DIAMENT et al.
1999.
Congenital myopathy with minimal changes: clinical and morphological aspects.
Eur j paediatr neurol.
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Health Sciences
Radiology, Nuclear Medicine and Imaging
Chong Ae KIM; Maria Rita Passos BUENO; Suley Kazue Nagahashi MARIE; Antonia M P CERQUEIRA; Umbertina Conti REED et al.
1999.
Clinical and molecular analysis of spinal muscular atrophy in brazilian patients.
Genetics and molecular biology.
Brasil.
22,
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487-492.
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Life Sciences
Neuroscience (miscellaneous)
Maria Luiza Giraldes De MANREZA; A E SCOTONI; E A SILVA; Carlos Alberto Mantovani GUERREIRO; E A P SILVA et al.
1999.
Estudo piloto com topiramato em crianças com síndrome de lennox-gastaut.
Arquivos de neuro-psiquiatria.
Brasil.
57,
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Life Sciences
Clinical Biochemistry
Juliana Gurgel GIANETTI; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Edmar ZANOTELLI et al.
1999.
Nebulin expression in patients with nemaline myopathy.
Neuromuscular disorders.
Inglaterra.
9,
513-513.
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Life Sciences
Neuroscience (miscellaneous)
Antonio Marcilio Padula OMURO; Mary Souza De CARVALHO; Umbertina Conti REED; Mariz VAINZOF; A S FERNANDES et al.
1999.
Relevance of the a8344g and t8356c mt mutation analyses in the approach of progressive myoclonic epilepsy.
Neurology.
Estados Unidos.
52,
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Health Sciences
Veterinary (miscellaneous)
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Mariz VAINZOF.
1999.
Rods proteic constitution and muscle fiber maturation in nemaline myopathy.
Neurology.
Estados Unidos.
52,
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Social Sciences & Humanities
Psychology (miscellaneous)
Marilisa M GUERREIRO; Maria Luiza Giraldes De MANREZA; A E SCOTONI; E A SILVA; Carlos Alberto Mantovani GUERREIRO et al.
1999.
A pilot study of topiramate in children with lennox-gastaut syndrome.
Arq neuropsiquiatr.
Brasil.
57,
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167-175.
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Health Sciences
Neurology (clinical)
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Alzira Alves De Siqueira CARVALHO; Luis Fernando FONSECA; Mary Souza De CARVALHO et al.
1999.
Kearns-sayre syndrome plus. classical clinical findings and dystonia.
Arq neuropsiquiatr.
Brasil.
57,
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Life Sciences
Genetics
Laura Maria De Figueiredo Ferreira GUILHOTO; Umbertina Conti REED; Elza Márcia Targas YACUBIAN; Maria Luiza Giraldes De MANREZA; Aron DIAMENT et al.
1998.
Aspectos evolutivos da síndrome landau-kleffner.
Arquivos de neuro-psiquiatria.
Brasil.
56,
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140-140.
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Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Juliana Elias Do Prado GURGEL; Adriana Ávila De ESPÍNDOLA; Mary Souza De CARVALHO.
1998.
Clinical variability of 3243 point mutation of mitochondrial dna in a brazilian casuistics.
Brain & development.
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368-368.
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Life Sciences
Neurology
Umbertina Conti REED; Juliana Elias Do Prado GURGEL; Mariz VAINZOF; Adriana Ávila De ESPÍNDOLA; Mary Souza De CARVALHO et al.
1998.
Congenital muscular dystrophy with cerebral matter hypodensity: report of 18 cases.
Brain & development.
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20,
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Health Sciences
Neurology (clinical)
Thelma Regina Correia MESSIAS; Tânia Virginia Fernandes SILVA; Fernando KOK; Andrea SCHAPPO; Hamilton MATUSHITA et al.
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Epilepsia e malformações cavernosas cerebrais familiares.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
93-93.
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Life Sciences
Animal Science and Zoology
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Mayana ZATZ et al.
1998.
Estudo imunohistoquímico da constituição protéica dos rods na miopatia nemalínica.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
69-69.
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Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; Monica S RUSTICCI; Viviana Silvia Helena Boccardi PALOU; C HAYASHIDA; Juliana Elias Do Prado GURGEL et al.
1998.
Frequência da mutação mitocondrial a3243g em pacientes com quadro clínico diferente.
Arquivos de neuro-psiquiatria.
Brasil.
56,
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73-73.
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Health Sciences
Neurology (clinical)
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Mary Souza De CARVALHO; Aron DIAMENT; Suely Kazue Nagahashi MARIE.
1998.
Inflammatory infiltration analysis in congenital muscular dystrophy.
Brain & development.
Japão.
20,
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385-385.
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Life Sciences
Genetics
Antonio Marcilio Padula OMURO; Alexandre Ribeiro FERNANDES; Mary Souza De CARVALHO; Monica S RUSTICCI; Umbertina Conti REED et al.
1998.
Merrf: correlações clínicas; histoquímicas e moleculares em uma família brasileira.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl.1)
130-131.
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Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Juliana Elias Do Prado GURGEL; Lucio Gobbo FERREIRA; Adriana Ávila De ESPÍNDOLA; Mary Souza De CARVALHO et al.
1998.
Merosin-positive congenital muscular dystrophy with involvement of the central nervous system.
Brain & development.
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383-383.
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Health Sciences
Medicine (miscellaneous)
Juliana Elias Do Prado GURGEL; Antonio Carlos De Padua MILAGRES; K M S C RODRIGUES; Maria Bernadete Dutra RESENDE; Umbertina Conti REED et al.
1998.
Miopatia associada ao vírus da imunodeficiência humana da infância: relato de um caso.
Arquivos de neuro-psiquiatria.
Brasil.
56,
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125-125.
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Health Sciences
Medicine (miscellaneous)
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Mary Souza De CARVALHO; Aron DIAMENT; Suely Kazue Nagahashi MARIE et al.
1998.
Miopatia congênita com anormalidades da linha z.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl.1)
68-69.
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Health Sciences
Medicine (miscellaneous)
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Mary Souza De CARVALHO; Aron DIAMENT; Suely Kazue Nagahashi MARIE et al.
1998.
Miopatia congênita com predomínio de fibras tipo ii.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
69-69.
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Health Sciences
Medicine (miscellaneous)
Juliana Elias Do Prado GURGEL; Umbertina Conti REED; Mary Souza De CARVALHO; Mariz VAINZOF; Aron DIAMENT et al.
1998.
Miopatia congênita minicore: curso progressivo em 3 irmãos.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
69-69.
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Health Sciences
Neurology (clinical)
Umbertina Conti REED; Laura Maria De Figueiredo Ferreira GUILHOTO; Maria Luiza Giraldes De MANREZA; Beatriz LEFÈVRE; L M PASTORELLO.
1998.
Síndrome de landau-kleffner: evolução clínica; abordagem neuropsicológica e fonoaudiológica de oito pacientes.
Brazilian journal of epidemiology and clinical neurophysiology.
Brasil.
4,
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Life Sciences
Genetics
Suely Kazue Nagahahsi MARIE; Alexandre Ribeiro FERNANDES; Juliana Elias Do Prado GURGEL; Monica S RUSTICCI; Umbertina Conti REED et al.
1998.
Síndrome de leigh: uma mutação t8993g de novo no dna mitocondrial.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
72-72.
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Life Sciences
Neurology
Virna Gonçalves TEIXEIRA; Mayana ZATZ; Maria Rita Passos BUENO; Mariz VAINZOF; Umbertina Conti REED et al.
1998.
Valor de alterações de neuroimagem em pacientes com distrofia miotônica.
Arquivos de neuro-psiquiatria.
Brasil.
56,
(supl. 1)
125-125.
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Life Sciences
Neurology
Laura Maria De Figueiredo Ferreira GUILHOTO; Umbertina Conti REED; Livia Cunha ELKIS; Suely Kazue Nagahashi MARIE; Aron DIAMENT.
1998.
Walker-walburg syndrome: a case report.
Brain & development.
Japão.
20,
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364-364.
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Life Sciences
Genetics
Umbertina Conti REED; Juliana Elias Do Prado GURGEL; Mariz VAINZOF; Adriana Avila De ESPÍNDOLA; Mary Souza De CARVALHO et al.
1998.
Evolutive aspects of landau - kleffner syndrome.
Am j hum genet.
Estados Unidos.
63,
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Health Sciences
Medicine (miscellaneous)
C A KIM; Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Maria Joaquina Marques DIAS; Maria Rita Passos BUENO et al.
1998.
Permanent mechanical ventilation in werdig-hoffmann disease: clinical and ethical aspects.
Am j hum genet.
Estados Unidos.
63,
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Health Sciences
Neurology (clinical)
Maria Luiza Giraldes De MANREZA; Laura Maria De Figueiredo Ferreira GUILHOTO; Beatriz LEFÈVRE; L M PASTORELLO; Umbertina Conti REED.
1998.
Clinical course in landau-kleffner syndrome is not correlated with density of epileptiform activity during acute phase of the disease.
Epilepsia.
Estados Unidos.
39,
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153-.
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Health Sciences
Medicine (miscellaneous)
Gurgel GEP; Sampaio LPB; Umbertina Conti REED; Mary Souza De CARVALHO; Suely Kazue Nagahashi MARIE.
1997.
Miopatia nemalínica; forma neonatal grave: evolução atípica em dois pacientes.
Revista de psiquiatria & psicanálise de crianças e adolescentes.
Brasil.
2,
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26-.
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Life Sciences
Genetics
Gurgel GEP; Sampaio LPB; Umbertina Conti REED; Mary Souza CARVALHO; Suely Kazue Nagahashi MARIE.
1997.
Miopatia vacuolar pas e fosfatase ácida positivas- correlação clínica-histoquímica em oito pacientes.
Revista de psiquiatria & psicanálise de crianças e adolescentes.
Brasil.
2,
26-.
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Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; Gurgel GEP; Adriana Avila De ESPÍNDOLA; Umbertina Conti REED; Mary Souza De CARVALHO et al.
1997.
Ponto de mutação 3243 do dna mitocondrial e suas variações fenotípicas.
Revista de psiquiatria & psicanálise de crianças e adolescentes.
Brasil.
2,
13-.
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Health Sciences
Neurology (clinical)
Mariz VAINZOF; Suely Kazue Nagahashi MARIE; Eloisa Sá MOREIRA; Umbertina Conti REED; José Antonio LEVY et al.
1997.
Deficiency of alfa-actinin-3 (actn3) occurs in different forms of muscular dystrophy.
Neuropediatrics.
Alemanha.
28,
223-228.
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Life Sciences
Neurology
A Gherpelli Jld Guerreiro Mm Costa Jc Rotta Nt Manreza MLG; Umbertina Conti REED; A Silva Ea Guerreiro Cam Nunes Ml PALMINI; L Vega GUTIÉRRZ; J VIZIOLI et al.
1997.
Vigabatrin in refractory childhood epilepsy. the brazilian multicenter study.
Epilepsy research.
Brasil.
29,
1-6.
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Social Sciences & Humanities
Psychology (miscellaneous)
José Luiz Dias GHERPELLI; Umbertina Conti REED.
1997.
Distúrbios do déficit da atenção - hiperatividade (ddah) - guia de atualização.
Pediatria moderna.
Brasil.
33,
(supl.)
113-120.
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Health Sciences
Neurology (clinical)
Maria Luiza Giraldes De MANREZA; Marilisa GUERREIRO; Viviane Borges FERREIRA; Umbertina Conti REED; Aron DIAMENT et al.
1997.
Long-term efficacy and safety of topiramate in lennox-gastaut syndrome.
Epilepsia.
Japão.
38,
(supl. 3)
98-98.
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Health Sciences
Radiology, Nuclear Medicine and Imaging
Virna Gonçalves TEIXEIRA; Mayana ZATZ; Suely Kazue Nagahashi MARIE; Maria Rita Passos BUENO; Umbertina Conti REED et al.
1997.
Correlation of dna expansion and systemic manifestations in myotonic dystrophy.
Journal of the neurological sciences.
Brasil.
150,
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Health Sciences
Genetics (clinical)
C S COSTA; Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Mayana ZATZ; Mariz VAINZOF.
1997.
Deficiência da proteína a-actinina 3 (actn3) em músculo de pacientes com distrofia muscular congênita.
Revista brasileira de genética.
Brasil.
21,
220-220.
-
Life Sciences
Neurology
Alzira Alves De Siqueira CARVALHO; Suely Kazue Nagahashi MARIE; Viviana Silvia Elena Boccardi PALOU; Mary Souza De CARVALHO; Umbertina Conti REED.
1997.
Immunocytochemical study of major histocompatibility complex i in neuromuscular disorders: the importance of differential diagnosis in inflamatory myopathies.
Journal of the neurological sciences.
Brasil.
150,
S175-S175.
-
Health Sciences
Neurology (clinical)
Alzira Alves De Siqueira CARVALHO; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Umbertina Conti REED.
1997.
Inclusion body myositis - sporadic form-atypical progression and anatomical follow-up.
Journal of the neurological sciences.
Brasil.
150,
S175-S175.
-
Health Sciences
Medicine (miscellaneous)
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Viviana Silvia Elena Boccardi PALOU; Mary Souza De CARVALHO; Alzira Alves De Siqueira CARVALHO.
1997.
Kearns-sayre syndrome: genetic correlation with muscle pathology and mri findings.
Journal of the neurological sciences.
Brasil.
150,
S259-S259.
-
Health Sciences
Neurology (clinical)
Marilisa M GUERREIRO; Maria Luiza Giraldes De MANREZA; Ferreira VB; Umbertina Conti REED; Aron J DIAMENT et al.
1997.
A pilot study of topiramate in children with lennox-gastaut syndrome.
Neurology.
Estados Unidos.
48,
(PO1.043)
A39-.
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Health Sciences
Cardiology and Cardiovascular Medicine
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Juliana Elias Do Prado GURGEL; Aron J DIAMENT.
1997.
Congenital fibre type disproportion myopathy. clinical course and prognosis.
J neurol sci.
Argentina.
150,
S122-.
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Health Sciences
Neurology (clinical)
Resende MBD; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary De Carvalho ALEGRO; Juliana Elias Do Prado GURGEL et al.
1997.
Minimal changes? myopathy. clinical course and prognosis.
J neurol sci.
Argentina.
150,
S322-.
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Life Sciences
Clinical Biochemistry
Juliana Elias Do Prado GURGEL; Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Mary Souza De CARVALHO; Palou V.
1997.
Desmin and vimentin analysis in nemaline myopathy.
J neurol sci.
Argentina.
150,
S121-.
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Life Sciences
Neurology
A A ESPINDOLA; Umbertina Conti REED; Suely Kazue Nagahashi MARIE; C A KIM; Juliana Elias Do Prado GURGEL et al.
1997.
Spinal muscular atrophy. clinical and genetic analysis of 28 cases.
J neurol sci.
Argentina.
150,
S313-.
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Health Sciences
Medicine (miscellaneous)
Resende MBD; Ramos FO; Hamani C; Umbertina Conti REED; Aron J DIAMENT.
1997.
Isquemia da artéria espinhal anterior como provável complicação de cateterização umbilical: relato de caso.
Revista de psiquiatria & psicanálise de crianças e adolescentes.
Brasil.
2,
(PO014)
31-.
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Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mariz VAINZOF; Eloisa Sá MOREIRA; José Antonio LEVY et al.
1996.
Congenital muscular dystrophy with cerebral white matter hypodensity. correlation of clinical features and merosin deficiency.
Brain & development (tokyo).
Japão.
18,
53-57.
-
Health Sciences
Medicine (miscellaneous)
Maria Luiza Giraldes De MANREZA; Marilisa GUERREIRO; Viviane Borges FERREIRA; Carlos Alberto Mantovani GUERREIRO; Aron DIAMENT et al.
1996.
Eficácia do topiramato em crianças com síndrome de lennox-gastaut.
Brazilian journal of epilepsy and clin. neurophysiology.
Brasil.
2,
86-86.
-
Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Chong Ae KIM; Maria Rita Passos BUENO; Alzira Alves De Siqueira CARVALHO et al.
1996.
Aep - estudo genético em família com heterogeneidade fenotípica.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
22-22.
-
Life Sciences
Genetics
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Alzira Alves De Siqueira CARVALHO; Mary De Carvalho ALEGRO; Eloisa Sá MOREIRA et al.
1996.
Dmc: forma pura ou clássica. análise clínica e revisão da classificação em 22 casos.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
43-43.
-
Health Sciences
Medicine (miscellaneous)
Patricia Soledad De SOUZA; Antonio Alberto ZAMBON; José Lamartine De ASSIS; Umbertina Conti REED; Paulo Eurípedes MARCHIORI.
1996.
Miastenia grave forma congênita familiar com apresentação cérvico-escapular.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
174-174.
-
Life Sciences
Neurology
Suely Kazue Nagahashi MARIE; Umbertina Conti REED; Mary De Carvalho ALEGRO; Alzira Alves De Siqueira CARVALHO; Helga Cristina Almeida De AZEVEDO et al.
1996.
Miopatia nemalínica: correlação clínico-histológica em 6 casos.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
44-44.
-
Health Sciences
Medicine (miscellaneous)
Fernando KOK; Leticia Pereira De BRITO; Umbertina Conti REED; Aron DIAMENT.
1996.
Sequencia da amioplasia congênita associada ao emprego durante a gestação de prostraglandina de uso veterinário: relato de caso.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
21-21.
-
Health Sciences
Medicine (miscellaneous)
Helga Cristina Almeida De AZEVEDO; J J LEITE; Mary De Carvalho ALEGRO; Eloisa Sá MOREIRA; Alzira Alves De Siqueira CARVALHO et al.
1996.
Teste de esforço cardiopulmonar nas miopatias.
Arquivos brasileiros de neuropsiquiatria.
Brasil.
54,
355-355.
-
Health Sciences
Neurology (clinical)
Chong Ae KIM; Maria Rita Passos BUENO; Suely Kazue Nagahashi MARIE; A M P CERQUEIRA; Umbertina Conti REED et al.
1996.
Molecular analysis of spinal muscular atrophy in brazilian patients.
Brazilian journal of genetic.
Brasil.
19,
(suppl.)
241-241.
-
Health Sciences
Neurology (clinical)
Helga Cristina Almeida De AZEVEDO; Lucia Iracema Zanotto De MENDONÇA; Paulo Nicolau Borsoi SALUM; Suely Kazue Nagahashi MARIE; Alzira Alves De Siqueira CANÇADO et al.
1996.
Miotonia congênita. relato de sete pacientes.
Arq neuropsiquiatr.
Brasil.
54,
595-600.
-
Health Sciences
Neurology (clinical)
Mariz VAINZOF; Suely Kazue Nagahashi MARIE; Umbertina Conti REED; J S SCHWARTZMAN; Rita C M PAVANELLO et al.
1995.
Deficiency of merosin (laminin m or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
Neuropediatrics.
Estados Unidos.
26,
293-296.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Suely Kazue Nagalhashi MARIE; Mario Wilson Iervolino BROTTO; Carlos Alberto MARTINEZ; Paulo Eurípedes MARCHIORI et al.
1995.
Autosomal recessive nondystrophic myotonia. report of a case with unusual clinical course.
Arq neuropsiquiatr.
Brasil.
53,
114-117.
-
Life Sciences
Neurology
José Luiz Dias GHERPELLI; Marilisa M GUERREIRO; Rotta NT; Costa JC; Maria Luiza Giraldes De MANREZA et al.
1995.
Vigabatrin in refractory childhood epilepsy. the brazilian multicenter study.
Epilepsia.
Austrália.
36,
(supl. 3)
S103-.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Passos Bueno MR; Suely Kazue Nagahashi MARIE; Antonia M P CERQUEIRA; Lucia Iracema Zanotto De MENDONÇA et al.
1994.
Distrofia miotônica. estudo da correlação clínico-genética em um par familiar (pai- filho).
Arq neuropsiquiatr.
Brasil.
52,
545-548.
-
Health Sciences
Cardiology and Cardiovascular Medicine
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Aron J DIAMENT; José Antonio LEVY.
1994.
Congenital structural myopathies: clinical and pathological review of 13 patients.
Pediatr neurol.
Estados Unidos.
11,
140-.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Suely Kazue Nagahashi MARIE; Ana Maria Crous TSANACLIS; Mary Souza De CARVALHO; Jaime ROIZENBLAT et al.
1994.
Congenital muscular dystrophy in two siblings with cataracts and slight cerebral involvement.
Pediatr neurol.
Brasil.
11,
141-.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Paulo Nicolau Borsoi SALUM; Aron J DIAMENT; José Antonio LEVY.
1994.
Congenital muscular dystrophy: clinical and pathological review of 24 patients.
Pediatr neurol.
Estados Unidos.
11,
141-.
-
Life Sciences
Neurology
José Luiz Dias GHERPELLI; Marilisa M GUERREIRO; Rotta NT; Costa JC; Maria Luiza Giraldes De MANREZA et al.
1994.
Vigabatrin in refractory childhood epilepsy: a multicenter study.
Pediatr neurol.
Estados Unidos.
11,
162-.
-
Life Sciences
Neurology
A Espíndola Aa Carvalho Ms DIAMENT; Maria Luiza Giraldes De MANREZA; Souza AMMH; Umbertina Conti REED; Aron J DIAMENT.
1994.
Single; small ct lesions in children with seizures.
Pediatric neurology.
Estados Unidos.
11,
116-.
-
Social Sciences & Humanities
Psychology (miscellaneous)
Laura Maria Ferreira GUILHOTO; Umbertina Conti REED; Silva LJB; Aron J DIAMENT.
1993.
Amiotrofia espinal infantil de evolução atípica. relato de dois casos.
Arq neuropsiquiatr.
Brasil.
51,
339-402.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Sérgio ROSEMBERG; José Luiz Dias GHERPELLI; Hamilton MATUSHITA; Gilberto G Machado De ALMEIDA et al.
1993.
Brain tumors in the first two years of life: a review of forty cases.
Pediatr neurosurg.
Estados Unidos.
19,
180-185.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Maria Luiza Giraldes De MANREZA; Aron J DIAMENT.
1993.
Epilepsy secondary to brain tumors in children.
Epilepsia.
Estados Unidos.
34,
(supl.2)
103-.
-
Life Sciences
Animal Science and Zoology
Suely Kazue Nagahashi MARIE; Mary Souza De CARVALHO; Umbertina Conti REED; Carvalho M; Paulo Nicolau Borsoi SALUM et al.
1993.
Stick-man: report of five cases of favorable evolution.
Canad j neurol sci.
Canadá.
20,
(S4)
S60-.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Ana Maria Crous TSANACLIS; Laura Maria De Figueiredo Ferreira GUILHOTO; Mary Souza De CARVALHO; Aron J DIAMENT et al.
1992.
Miopatia centronuclear (miotubular): relato de caso.
Rev hosp clin fac med s paulo.
Brasil.
47,
237-239.
-
Social Sciences & Humanities
Psychology (miscellaneous)
Paulo Henrique Pires De AGUIAR; Hamilton MATUSHITA; Orildo Ciquini JUNIOR; Sérgio ROSEMBERG; Umbertina Conti REED et al.
1991.
Síndrome de russell: relato de dois casos.
Arq neuropsiquiatr.
Brasil.
10,
39-46.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Matsuhita H; Rosemberg S; Gilberto G Machado De ALMEIDA; Aron J DIAMENT.
1990.
Brain tumors in children of less than two years of age.
Brain development.
Japão.
12,
(TL003)
623-.
-
Health Sciences
Neurology (clinical)
Umbertina Conti REED; Hamilton MATUSHITA; Rosemberg S; Gilberto G Machado De ALMEIDA; Aron J DIAMENT.
1990.
Supratentorial brain tumors in children.
Brain development.
Japão.
12,
(PO204)
716-.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Hamilton MATUSHITA; Rosemberg S; Gilberto G Machado De ALMEIDA; Aron J DIAMENT.
1990.
Brain tumors in children. a statistical study.
Brain development.
Japão.
12,
(PO203)
716-.
-
Social Sciences & Humanities
Psychology (miscellaneous)
Umbertina Conti REED; Olazabal PJC; Livia Cunha ELKIS; Aron J DIAMENT.
1986.
Síndrome dos polegares aduzidos. relato de um caso e revisão da literatura.
Anais do 12o congresso brasileiro de neurologia.
Brasil.
25.09-.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Sérgio ROSEMBERG; Milberto SCAFF; Horácio Martins CANELAS; Aron J DIAMENT et al.
1984.
Síndrome de menkes: revisão da patogenia a propósito de um caso anátomo-clínico.
Arq neuropsiquiatr.
Brasil.
42,
262-273.
-
Health Sciences
Pediatrics, Perinatology and Child Health
Maria Cristina BELTRAMI; Umbertina Conti REED; Aron J DIAMENT.
1984.
Tumores intracranianos no grupo etário de zero a 2 anos.
Anais do xi congresso brasileiro de neurologia.
Brasil.
(TL8)
92-.
-
Health Sciences
Neurology (clinical)
Munhoz PSJ; Umbertina Conti REED; Andrade AF; Aron J DIAMENT; Gilberto G Machado De ALMEIDA.
1983.
Hematoma primário de tronco cerebral. registro de um caso.
Arq bras neurocir.
Brasil.
2,
285-289.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED.
1982.
Tumores raros de fossa posterior na infância.
Arq bras neurocir.
Brasil.
1,
27-38.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED.
1982.
Tumores da fossa posterior em crianças. aspectos clínicos.
Rev hosp clín fac med s paulo.
Brasil.
37,
219-227.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Aron J DIAMENT; Horácio Martins CANELAS; Antonio Branco LEFÈVRE.
1982.
Síndrome de menkes - apresentação de 1 caso.
Anais do x congresso brasileiro de neurologia e vii reunião da liga brasileira de epilepsia.
Brasil.
((TL5))
93-.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED; Gilberto G Machado De ALMEIDA; Antonio Branco LEFÈVRE; Sallum J.
1979.
Teratoma do iv ventrículo e puberdade precoce.
Arq neuropsiquiatr.
Brasil.
37,
319-327.
-
Health Sciences
Medicine (miscellaneous)
Umbertina Conti REED.
1977.
Tumores do sistema nervoso central na infância.
Clínica pediátrica.
Brasil.
1,
(10)
4-23.
-
Health Sciences
Veterinary (miscellaneous)
Umbertina Conti REED; Bresolin AU; Antonio Branco LEFÈVRE.
1975.
Granuloma eosinófilo de coluna cervical com manifestações neurológicas; liquóricas e radiológicas atípicas.
Arq neuropsiquiatr.
Brasil.
33,
168-177.
-
Life Sciences
Neuroscience (miscellaneous)
José Píndaro Pereira PLESE; Walter Carlos PEREIRA; Umbertina Conti REED; Antonio Branco LEFÈVRE.
1974.
Abscessos cerebelares. considerações a propósito de 4 casos em crianças.
Arq neuropsiquiatr.
Brasil.
32,
217-221.