Chong Ae Kim

Dados pessoais

Publicações

Total: 988

Área temática ASJC

Percentual das publicações classificadas

  • HS Ciências da Saúde
  • LS Ciências da Vida
  • MU Multidisciplinar
  • PS Ciências Físicas
  • SH Ciências Sociais e Humanidades

Categoria ASJC

Categorias ASJC mais frequentes

Termos frequentes nas publicações

Nuvem de termos dos títulos das publicações
Nome Vínculo Links Grande área de atuação Área de atuação
Carla Gentile MATAS Ciências da Saúde Fonoaudiologia
Carlos Augusto Galvão BARBOZA Ciências Biológicas Morfologia
Celia Priszkulnik KOIFFMANN Ciências Biológicas Genética
Claudia Berlim De MELLO Ciências Humanas Psicologia
Dafne Dain Gandelman HOROVITZ Ciências da Saúde Medicina
Débora Gusmão MELO Ciências da Saúde Medicina
Débora Maria Befi LOPES Membro Ciências da Saúde Fonoaudiologia
Decio BRUNONI Ciências Biológicas Genética
Erasmo Barbante CASELLA Ciências da Saúde Medicina
Fernanda Tebexreni ORSATI Ciências Humanas Psicologia
Juan Clinton Llerena JUNIOR Ciências da Saúde Medicina
Luiz Renato Rodrigues CARREIRO Ciências Humanas Psicologia
Márcia Helena Da Silva MELO Ciências Humanas Psicologia
Milena Coelho Fernandes CALDATO Ciências da Saúde Medicina
Paulo Ricardo Gazzola ZEN Ciências da Saúde Medicina
Paulo Sérgio BOGGIO Membro Ciências Biológicas Fisiologia
Roberto GIUGLIANI Membro Ciências Biológicas Genética
Vânia D ALMEIDA Membro Ciências Biológicas Bioquímica
Figura 1

Número de publicações por ano e por tipo

Todas as publicações do perfil

Figura 2

Categorias ASJC mais frequentes por ano

A cor dos pontos identifica a categoria predominante

Figura 3

Mapa de calor das categorias ASJC por ano

Frequências absolutas; cores mais escuras indicam mais publicações. Todas as categorias ASJC e anos disponíveis, sem aplicar os filtros da página.

Escala: 0 → 17

Mapa de calor das categorias ASJC por ano
Categoria ASJC19801983198419851986198719881989199119921993199419951996199719981999200020012002200320042005200620072008200920102011201220132014201520162017201820192020202120222023202420252026
1311 · Genetics0101200061142924176442613118756128111071110352481171
2716 · Genetics (clinical)1000001220011753111091191512233611083557837458101042
2701 · Medicine (miscellaneous)211011022556014546777204105571563256460250000
2735 · Pediatrics; Perinatology and Child Health10120002023632132225122031120111212100123101
3201 · Psychology (miscellaneous)01000000133542511002111001121121000220040000
2728 · Neurology (clinical)10001100001231101203213301100311132031112000
2808 · Neurology00000001100121212551020110412300002400200000
2801 · Neuroscience (miscellaneous)00000100002001110130010111101051032101000000
1301 · Biochemistry; Genetics and Molecular Biology (miscellaneous)00000000000010011001000010202211000301001000
1312 · Molecular Biology00000000000000101000000010110001100000101001
2710 · Embryology00000001001001012100110000010000000000000000
2712 · Endocrinology; Diabetes and Metabolism00000000001000000000000001020000000001003100
2741 · Radiology; Nuclear Medicine and Imaging00000000000100001000040011000000001000000000
1309 · Developmental Biology00000000000000000001000000020000000021000110
2705 · Cardiology and Cardiovascular Medicine00000000000000000010101000000020100000110000
2738 · Psychiatry and Mental Health00000000101000000000100000021010000000010000
3304 · Education00000001000110000001001000000010001000000000
2725 · Infectious Diseases00000000000000000011001000002000010000000000
1308 · Clinical Biochemistry00000000001000000010001100000000100000000000
2700 · General Medicine00000000100001010000000000000000001000000100
2734 · Pathology and Forensic Medicine00000000000000002000200000000000000000000100
1203 · Language and Linguistics10000000001100000000000000000000000000100000
3616 · Speech and Hearing00000000110000001000000000000000000100000000
1103 · Animal Science and Zoology00000000000000020000000000000001000000000000
1702 · Artificial Intelligence00000000001000000000000000000010000000100000
2723 · Immunology and Allergy00000000000000001000000000000101000000000000
2204 · Biomedical Engineering00000000000000000010000000000100000000000000
2708 · Dermatology00000000000000000000000000100000000000000100
2713 · Epidemiology00000000000000000000000000000000000000010100
2715 · Gastroenterology00000000000000000000000000000000000000000020
2724 · Internal Medicine00000000000000000100000000001000000000000000
2731 · Ophthalmology00000000000000000000000000000100000000000010
2732 · Orthopedics and Sports Medicine00000000000000000001000000000100000000000000
2736 · Pharmacology (medical)00000000000000100000000000010000000000000000
3310 · Linguistics and Language00000000000101000000000000000000000000000000
1300 · General Biochemistry; Genetics and Molecular Biology00000000000000000000000000000100000000000000
1302 · Aging00000000000000000000000000010000000000000000
1303 · Biochemistry00000000000000000001000000000000000000000000
1310 · Endocrinology00000000000000000000000010000000000000000000
1313 · Molecular Medicine00000000000000000000000000000000000000100000
1314 · Physiology00000000000000000000010000000000000000000000
1402 · Accounting00000000000000000000000000000000000000001000
2301 · Environmental Science (miscellaneous)00000000000000000100000000000000000000000000
2401 · Immunology and Microbiology (miscellaneous)00000000000000000000000000000001000000000000
2405 · Parasitology00000000000100000000000000000000000000000000
2702 · Anatomy00000000000000000000000000000000000010000000
2704 · Biochemistry (medical)00000000000000000000000000100000000000000000
2720 · Hematology00000000000000000000100000000000000000000000
2722 · Histology00000000000000000000000000010000000000000000
2727 · Nephrology00000000000000000000010000000000000000000000
2730 · Oncology00000000000000000000001000000000000000000000
2733 · Otorhinolaryngology00000000000000000000000000000000000000000100
2739 · Public Health; Environmental and Occupational Health00000000000001000000000000000000000000000000
2746 · Surgery00000000000000000000000000000000010000000000
2803 · Biological Psychiatry00000000000000000000000000000100000000000000
2806 · Developmental Neuroscience00000000000000000000100000000000000000000000
2809 · Sensory Systems00000000000000000000000000000000000000001000
2919 · Pediatrics00000000000000000000000000000000000010000000
3001 · Pharmacology; Toxicology and Pharmaceutics (miscellaneous)00000000000000000000000000000000000100000000
3203 · Clinical Psychology00000000000000000000000000100000000000000000
3204 · Developmental and Educational Psychology00000000000000000000000000000000001000000000
3206 · Neuropsychology and Physiological Psychology00000000000000000000000000001000000000000000
3300 · General Social Sciences00000000000000000000000000000000000000010000
3607 · Medical Laboratory Technology00000000000000001000000000000000000000000000
988 publicação(ões)
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Ano Tipo Registro Área temática e categoria ASJC
2004 Trabalho em evento
Monozygotic twins discordant for cystic microphthalmia; abnormalities of first branchial arch and midline structures: a variant of oculocerebrocutaneous syndrome? Chong Ae KIM; L M J ALBANO; L R S SADECK; C R LEONE; G J F GATTÁS et al Annual Clinical Genetics Meeting of American College of Medical Genetics
HS Neurology (clinical)
2004 Trabalho em evento
Omodysplasia: report of the first Brazilian case L M J ALBANO; L A N OLIVEIRA; D R BERTOLA; A C PAULA; T P DELBONI et al 54th Annual Meeting of the American Society of Human Genetics
LS Neurology
2004 Trabalho em evento
Radiologic manifestations of 5 brazilian cases of mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome) A C PAULA; A C G M SANTOS; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al 54th Annual Meeting of the American Society of Human Genetics
LS Genetics
2004 Trabalho em evento
Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient Debora Romeo BERTOLA; A C PEREIRA; P S OLIVEIRA; L MESSIAEN; B D GELB et al 54th Annual Meeting of the American Society of Human Genetics
LS Neurology
2004 Trabalho em evento
Noonan-like phenotype and PTPN11 gene: study of 15 patients Chong Ae KIM; A C PEREIRA; J KRIEGER; L M J ALBANO; Debora Romeo BERTOLA 54th Annual Meeting of the American Society of Human Genetics
LS Genetics
2004 Trabalho em evento
Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly - screening for loss of heterozigosity in 9p and 11q regions F S JEHEE; D JOHNSON; K T ABE; L ALONSO; N ALONSO et al 54th Annual Meeting of the American Society of Human Genetics
HS Genetics (clinical)
2004 Trabalho em evento
Is the Prader-Willi Syndrome phenotype related to molecular mechanisms? A study of 75 patients M C VARELA; F KOK; N SETIAN; Chong Ae KIM; C P KOIFFMANN 54th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2004 Trabalho em evento
Oral defects of brazilian cases of mucopolysaccharidosis A C G M SANTOS; A PAULA; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al 54th Annual Meeting of the American Society of Human Genetics
LS Genetics
2004 Trabalho em evento
Anomalias congênitas associadas ao uso do Misoprostol no 1º trimestre de gestação: estudo clínico de 11 novos casos Maria Joaquina Marques DIAS; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; J A PAZ; E DINIZ et al XIV Congresso Brasileiro de Perinatologia- XI Reunião de Enfermagem Perinatal
HS Pediatrics; Perinatology and Child Health
2004 Trabalho em evento
Isolation of a peptide linked keratan sulphate from urine of a patient with Morquio Syndrome V J Coulson THOMAS; Y M MICHELACCI; T G FERREIRA; Chong Ae KIM; L M J ALBANO et al SIMEC International Symposium on Extracellular Matrix
HS Genetics (clinical)
2004 Trabalho em evento
Achados radiológicos em pacientes com Mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) Ana Carolina PAULA; A C G M SANTOS; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al XVI Congresso Brasileiro de Genética Clínica
HS Radiology; Nuclear Medicine and Imaging
2004 Trabalho em evento
Galactosialidose: relato de tres casos com início precoce. L M J ALBANO; M SANO; L YANO; E DINIZ; D R BERTOLA et al XVI Congresso Nacional de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Estudo de correlação genótipo-fenótipo em seis brasileiros portadores da mutação 1533del23 A C M AZEVEDO; I SCHWATZ; M PETRY; A P BEHEREGARAY; F T SOUZA et al XVI Congresso Nacional de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Omodisplasia: relato do primeiro caso brasileiro L ALBANO; L A N OLIVEIRA; D R BERTOLA; A C PAULA; T P DELBONI et al XVI Congresso Nacional de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Achados radiológicos em pacientes com mucopolissacaridose Ana Carolina PAULA; A C G M SANTOS; T P DELBONI; D R BEROLA; L M J ALBANO et al XVI Congresso Nacional de Genética Clínica
HS Radiology; Nuclear Medicine and Imaging
2004 Trabalho em evento
Further evidence that the T731 PTPN11 gene mutation is associated with myeloproliferative disorder in Noonan syndrome Debora Romeo BERTOLA; A C PEREIRA; J D A CARNEIRO; J KRIEGER; Chong Ae KIM Annual Clinical Genetics Meeting of American College of Medical Genetics
LS Genetics
2004 Artigo em periódico
Serum leptin level is a regulator of bone mass F ELEFTEROIUS; S TAKEDA; K EBIHARA; J MAGRE; N PATANO et al PNAS. Proceedings of the National Academy of Sciences of the United States of America ISSN 0027-8424
LS Physiology
2004 Artigo em periódico
Mutations in the gene encoding filamin B disrupt vertebral segmentation; joint formation and skeletogenesis D KRAKOW; S P ROBERTSON; L M KING; T MORGAN; E T SEBALD et al Nature Genetics ISSN 1061-4036
LS Genetics
2004 Artigo em periódico
Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telengiectasia: seven new mutations. G COUTINHO; M MITUI; C CAMBELL; B T C CARVALHO; S NAHAS et al American Journal of Medical Genetics. Part A ISSN 1552-4825
HS Genetics (clinical)
2004 Artigo em periódico
Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis L M J ALBANO; P P O SAKAE; M M G B MATALOUN; C R LEONE; D R BERTOLA et al Clinics (USP. Impresso) ISSN 1807-5932
HS Embryology
2004 Artigo em periódico
Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia; type Maroteaux. C F BARTELS; H BUKULMEZ; P PADAYATTI; D K RHEE; C Van SHIH et al American Journal of Human Genetics ISSN 0002-9297
HS Genetics (clinical)
2004 Artigo em periódico
Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome at variable expression of a single genetic disorder. D R BERTOLA; Chong Ae KIM; L Mj ALBANO; H SCHEFFER; R MEIJER et al Clinical Genetics ISSN 0009-9163
LS Genetics
2004 Artigo em periódico
Clinical and biochemical study of 28 patients with mucopolysaccharidose type VI. A C AZEVEDO; I V SCHWARTZ; L KALAKUN; S BRUSTOLIN; M G BURLIN et al Clinical Genetics ISSN 0009-9163
HS Genetics (clinical)
2004 Artigo em periódico
Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation. D R BEROLA; A C PEREIRA; P S OLIVEIRA; Chong Ae KIM; J E KRIEGER American Journal of Medical Genetics. Part A ISSN 1552-4825
HS Genetics (clinical)
2004 Artigo em periódico
Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH) S M M SUGAYAMA; V H KOCH; E A FURUSAWA; C LEONE; Chong Ae KIM Clinics (USP. Impresso) ISSN 1807-5932
HS Nephrology
2004 Trabalho em evento
HS Neurology (clinical)

Monozygotic twins discordant for cystic microphthalmia; abnormalities of first branchial arch and midline structures: a variant of oculocerebrocutaneous syndrome?

Annual Clinical Genetics Meeting of American College of Medical Genetics

Chong Ae KIM; L M J ALBANO; L R S SADECK; C R LEONE; G J F GATTÁS et al

2004 Trabalho em evento
LS Neurology

Omodysplasia: report of the first Brazilian case

54th Annual Meeting of the American Society of Human Genetics

L M J ALBANO; L A N OLIVEIRA; D R BERTOLA; A C PAULA; T P DELBONI et al

2004 Trabalho em evento
LS Genetics

Radiologic manifestations of 5 brazilian cases of mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)

54th Annual Meeting of the American Society of Human Genetics

A C PAULA; A C G M SANTOS; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al

2004 Trabalho em evento
LS Neurology

Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient

54th Annual Meeting of the American Society of Human Genetics

Debora Romeo BERTOLA; A C PEREIRA; P S OLIVEIRA; L MESSIAEN; B D GELB et al

2004 Trabalho em evento
LS Genetics

Noonan-like phenotype and PTPN11 gene: study of 15 patients

54th Annual Meeting of the American Society of Human Genetics

Chong Ae KIM; A C PEREIRA; J KRIEGER; L M J ALBANO; Debora Romeo BERTOLA

2004 Trabalho em evento
HS Genetics (clinical)

Genetic and molecular analysis of a large cohort of patients with syndromic and non-syndromic trigonocephaly - screening for loss of heterozigosity in 9p and 11q regions

54th Annual Meeting of the American Society of Human Genetics

F S JEHEE; D JOHNSON; K T ABE; L ALONSO; N ALONSO et al

2004 Trabalho em evento
HS Medicine (miscellaneous)

Is the Prader-Willi Syndrome phenotype related to molecular mechanisms? A study of 75 patients

54th Annual Meeting of the American Society of Human Genetics

M C VARELA; F KOK; N SETIAN; Chong Ae KIM; C P KOIFFMANN

2004 Trabalho em evento
LS Genetics

Oral defects of brazilian cases of mucopolysaccharidosis

54th Annual Meeting of the American Society of Human Genetics

A C G M SANTOS; A PAULA; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al

2004 Trabalho em evento
HS Pediatrics; Perinatology and Child Health

Anomalias congênitas associadas ao uso do Misoprostol no 1º trimestre de gestação: estudo clínico de 11 novos casos

XIV Congresso Brasileiro de Perinatologia- XI Reunião de Enfermagem Perinatal

Maria Joaquina Marques DIAS; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; J A PAZ; E DINIZ et al

2004 Trabalho em evento
HS Genetics (clinical)

Isolation of a peptide linked keratan sulphate from urine of a patient with Morquio Syndrome

SIMEC International Symposium on Extracellular Matrix

V J Coulson THOMAS; Y M MICHELACCI; T G FERREIRA; Chong Ae KIM; L M J ALBANO et al

2004 Trabalho em evento
HS Radiology; Nuclear Medicine and Imaging

Achados radiológicos em pacientes com Mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy)

XVI Congresso Brasileiro de Genética Clínica

Ana Carolina PAULA; A C G M SANTOS; T P DELBONI; Debora Romeo BERTOLA; L M J ALBANO et al

2004 Trabalho em evento
HS Genetics (clinical)

Galactosialidose: relato de tres casos com início precoce.

XVI Congresso Nacional de Genética Clínica

L M J ALBANO; M SANO; L YANO; E DINIZ; D R BERTOLA et al

2004 Trabalho em evento
HS Genetics (clinical)

Estudo de correlação genótipo-fenótipo em seis brasileiros portadores da mutação 1533del23

XVI Congresso Nacional de Genética Clínica

A C M AZEVEDO; I SCHWATZ; M PETRY; A P BEHEREGARAY; F T SOUZA et al

2004 Trabalho em evento
HS Genetics (clinical)

Omodisplasia: relato do primeiro caso brasileiro

XVI Congresso Nacional de Genética Clínica

L ALBANO; L A N OLIVEIRA; D R BERTOLA; A C PAULA; T P DELBONI et al

2004 Trabalho em evento
HS Radiology; Nuclear Medicine and Imaging

Achados radiológicos em pacientes com mucopolissacaridose

XVI Congresso Nacional de Genética Clínica

Ana Carolina PAULA; A C G M SANTOS; T P DELBONI; D R BEROLA; L M J ALBANO et al

2004 Trabalho em evento
LS Genetics

Further evidence that the T731 PTPN11 gene mutation is associated with myeloproliferative disorder in Noonan syndrome

Annual Clinical Genetics Meeting of American College of Medical Genetics

Debora Romeo BERTOLA; A C PEREIRA; J D A CARNEIRO; J KRIEGER; Chong Ae KIM

2004 Artigo em periódico
LS Physiology

Serum leptin level is a regulator of bone mass

PNAS. Proceedings of the National Academy of Sciences of the United States of America

F ELEFTEROIUS; S TAKEDA; K EBIHARA; J MAGRE; N PATANO et al

ISSN 0027-8424
2004 Artigo em periódico
LS Genetics

Mutations in the gene encoding filamin B disrupt vertebral segmentation; joint formation and skeletogenesis

Nature Genetics

D KRAKOW; S P ROBERTSON; L M KING; T MORGAN; E T SEBALD et al

ISSN 1061-4036
2004 Artigo em periódico
HS Genetics (clinical)

Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telengiectasia: seven new mutations.

American Journal of Medical Genetics. Part A

G COUTINHO; M MITUI; C CAMBELL; B T C CARVALHO; S NAHAS et al

ISSN 1552-4825
2004 Artigo em periódico
HS Embryology

Hydronephrosis in Schinzel-Giedion syndrome: an important clue for the diagnosis

Clinics (USP. Impresso)

L M J ALBANO; P P O SAKAE; M M G B MATALOUN; C R LEONE; D R BERTOLA et al

ISSN 1807-5932
2004 Artigo em periódico
HS Genetics (clinical)

Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia; type Maroteaux.

American Journal of Human Genetics

C F BARTELS; H BUKULMEZ; P PADAYATTI; D K RHEE; C Van SHIH et al

ISSN 0002-9297
2004 Artigo em periódico
LS Genetics

Molecular evidence that AEC syndrome and Rapp-Hodgkin syndrome at variable expression of a single genetic disorder.

Clinical Genetics

D R BERTOLA; Chong Ae KIM; L Mj ALBANO; H SCHEFFER; R MEIJER et al

ISSN 0009-9163
2004 Artigo em periódico
HS Genetics (clinical)

Clinical and biochemical study of 28 patients with mucopolysaccharidose type VI.

Clinical Genetics

A C AZEVEDO; I V SCHWARTZ; L KALAKUN; S BRUSTOLIN; M G BURLIN et al

ISSN 0009-9163
2004 Artigo em periódico
HS Genetics (clinical)

Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation.

American Journal of Medical Genetics. Part A

D R BEROLA; A C PEREIRA; P S OLIVEIRA; Chong Ae KIM; J E KRIEGER

ISSN 1552-4825
2004 Artigo em periódico
HS Nephrology

Renal and urinary findings in 20 patients with Williams-Beuren syndrome diagnosed by fluorescence in situ hybridization (FISH)

Clinics (USP. Impresso)

S M M SUGAYAMA; V H KOCH; E A FURUSAWA; C LEONE; Chong Ae KIM

ISSN 1807-5932