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
2010 Capítulo de livro
Envelhecimento precoce Chong Ae KIM; L M J ALBANO; Debora Romeo BERTOLA Genética na Prática Pediátrica ISBN 9788520428610
LS Aging
2010 Capítulo de livro
Síndromes com risco aumentado de desenvolvimento de tumores Rachel Sayuri HONJO; Isabel Mosca FURQUIM; Chong Ae KIM; L M J ALBANO Genética na Prática Pediátrica ISBN 9788520428610
HS Medicine (miscellaneous)
2010 Capítulo de livro
Doenças de depósito lisossômico Ana Carolina PAULA; Chong Ae KIM; L M J ALBANO Genética na Prática Pediátrica ISBN 9788520428610
HS Medicine (miscellaneous)
2010 Capítulo de livro
Teratógenos Camila Rebelo NICOLAU; Chong Ae KIM; Debora Romeo BERTOLA Genética na Prática Pediátrica ISBN 9788520428610
HS Pharmacology (medical)
2010 Livro
Genética na Prática Pediátrica Chong Ae KIM; L M J ALBANO; D R BERTOLA — ISBN 9788520428610
HS Genetics (clinical)
2010 Trabalho em evento
Cardiac findings in 61 Noonan syndrome patients with proven mutations in genes of the RAS/MAPK signaling pathway Debora Romeo BERTOLA; A S BRASIL; Alexander A L JORGE; A C MALAQUIAS; Luciana T WANDERLEY et al European Human Genetics Conference 2010
HS Medicine (miscellaneous)
2010 Trabalho em evento
High frequency of autistic traits in Williams-beuren patients Chong Ae KIM; Francisco B Assumpção JUNIOR; Rachel Sayuri HONJO; Roberta Lelis DUTRA; Vera A S AMARAL et al European Human Genetics Conference 2010
LS Genetics
2010 Trabalho em evento
Mechanisms of Ring Chromosome Formation Maria Isabel MELARAGNO; V A F MELONI; Chong Ae KIM; Rachel Sayuri HONJO; D M CHRISTOFOLINI et al European Human Genetics Conference 2010
LS Genetics
2010 Trabalho em evento
First Brazilian Case of Lysinuric Protein Intolerance (LPI) Isabel Mosca FURQUIM; Rachel Sayuri HONJO; C M LOURENÇO; T MAUAD; D R BERTOLA et al European Human Genetics Conference 2010
LS Genetics
2010 Trabalho em evento
Enzyme replacement therapy in 25 mucopolyssaccharidosis type VI Brazilian children under five years Dafne HOROVITZ; T P C MAGALHÃES; A ACOSTA; E M RIBEIRO; L GIUGLIANI et al 11th International Symposium on Mucopolysaccharide and related diseases
HS Genetics (clinical)
2010 Trabalho em evento
Replacement therapy in mucopolysaccharidosis typi VI: Advantages of early onset of treatment regarding cardiac involvement G N LEAL; Ana Carolina PAULA; Chong Ae KIM 11th International Symposium on Mucopolysaccharide and related disease
HS Pediatrics; Perinatology and Child Health
2010 Trabalho em evento
Genotype-phenotype delineation of terminal deletions 18q demonstrating high phenotypic variability L D KULIKOWSKI; M YOSHIMOTO; C M MONMA; F T S BELLUCCO; S I N BELANGERO et al European Human Genetics Conference 2010
LS Genetics
2010 Artigo em periódico
Alterações comportamentais na Síndrome de Noonan: dados preliminares brasileiros. Erica R MOTA; D R BERTOLA; Chong Ae KIM; Maria Cristina T V TEIXEIRA Revista Latinoamericana de Psicología ISSN 0120-0534
HS Psychiatry and Mental Health
2010 Artigo em periódico
Williams-Beuren syndrome:Diagnosis by polymorphic markers Ivanete Chaves SBRUZZI; A C PEREIRA; Beatriz VASCONCELOS; Rachel Sayuri HONJO; J E KRIEGER et al Genetic Testing ISSN 1090-6576
LS Genetics
2010 Artigo em periódico
Fenótipo comportamental de crianças e adolescentes com síndrome de Prader-Willi Maria Luiza G De MESQUITA; Decio BRUNONI; João Monteiro De Pina NETO; Chong Ae KIM; Márcia Helena S MELO et al Revista Paulista de Pediatria (Impresso) ISSN 0103-0582
SH Psychology (miscellaneous)
2010 Artigo em periódico
Echocardiographic study of paediatric patients with mucopolycaccharidosis G N LEAL; Ana Carolina PAULA; C LEONE; Chong Ae KIM Cardiology in the Young ISSN 1047-9511
HS Medicine (miscellaneous)
2010 Artigo em periódico
PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-like syndromes A S BRASIL; A C PEREIRA; Luciana T WANDERLEY; Chong Ae KIM; A C MALAQUIAS et al Genetic Testing ISSN 1090-6576
LS Genetics
2010 Artigo em periódico
Craniosynostosis in Pycnodysostosis: Broading the Spectrum of the Cranial Flat Bone Abnormalities Debora Romeo BERTOLA; Cassio AMARAL; Chong Ae KIM; L M J ALBANO; Meire AGUENA et al American Journal of Medical Genetics. Part A ISSN 1552-4825
HS Genetics (clinical)
2010 Artigo em periódico
DiGeorge syndrome: a not so rare syndrome A B F FOMIN; A C PASTORINO; Chong Ae KIM; A C PEREIRA; M Carneiro SAMPAIO et al Clinics (USP. Impresso) ISSN 1807-5932
HS Medicine (miscellaneous)
2010 Artigo em periódico
Enzyme replacement the therapy fro mucopolysaccharidoses: I;II and VI: recommendation from a group of brazilian F experts Roberto GIUGLIANI; A FEDERHEN; M V MUNOZ; T A VIEIRA; O ARTIGALÁS et al Revista da Associação Médica Brasileira (1992. Impresso) ISSN 0104-4230
HS Genetics (clinical)
2010 Artigo em periódico
Two Distinct Regions in 2q24.2-q24.3 Associated with Idiopathic Epilepsy A C Krepischi SANTOS; J KNIJNENBURG; D R BEROLA; Chong Ae KIM; P L PEARSON et al Epilepsia (Copenhagen) ISSN 0013-9580
LS Neurology
2010 Artigo em periódico
Behavioral and cognitive phenotype of children and adolescent with Williams-Beuren syndrome Maria Cristina T V TEIXEIRA; Camila Rondinelli Cobra MONTEIRO; Renata De Lima VELLOSO; Chong Ae KIM; Luiz Renato Rodrigues CARREIRO Pró-Fono (Impresso) ISSN 0104-5687
SH Psychology (miscellaneous)
2010 Artigo em periódico
All Ilustrative Case of Neurofibromatosis type 1 and NF1Microdeletion L A PRAXEDES; F M PEREIRA; Juliana MAZZEU; S S COSTA; Debora Romeo BERTOLA et al Molecular Syndromology ISSN 1661-8769
LS Molecular Biology
2010 Artigo em periódico
Co-ocurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype? A S BRASIL; Chong Ae KIM; J KRIEGER; A C PEREIRA; Debora Romeo BERTOLA Arquivos Brasileiros de Endocrinologia e Metabologia (Impresso) ISSN 0004-2730
HS Endocrinology; Diabetes and Metabolism
2010 Artigo em periódico
Obesity in Pycnodisostosis due to UPD1: Possible effect of an Imprinted gene in Chromosome 1 Debora Romeo BERTOLA; Meire AGUENA; G L YAMAMOTO; Chong Ae KIM; M R Passo BUENO American Journal of Medical Genetics. Part A ISSN 1552-4825
HS Genetics (clinical)
2010 Capítulo de livro
LS Aging

Envelhecimento precoce

Genética na Prática Pediátrica

Chong Ae KIM; L M J ALBANO; Debora Romeo BERTOLA

ISBN 9788520428610
2010 Capítulo de livro
HS Medicine (miscellaneous)

Síndromes com risco aumentado de desenvolvimento de tumores

Genética na Prática Pediátrica

Rachel Sayuri HONJO; Isabel Mosca FURQUIM; Chong Ae KIM; L M J ALBANO

ISBN 9788520428610
2010 Capítulo de livro
HS Medicine (miscellaneous)

Doenças de depósito lisossômico

Genética na Prática Pediátrica

Ana Carolina PAULA; Chong Ae KIM; L M J ALBANO

ISBN 9788520428610
2010 Capítulo de livro
HS Pharmacology (medical)

Teratógenos

Genética na Prática Pediátrica

Camila Rebelo NICOLAU; Chong Ae KIM; Debora Romeo BERTOLA

ISBN 9788520428610
2010 Livro
HS Genetics (clinical)

Genética na Prática Pediátrica

—

Chong Ae KIM; L M J ALBANO; D R BERTOLA

ISBN 9788520428610
2010 Trabalho em evento
HS Medicine (miscellaneous)

Cardiac findings in 61 Noonan syndrome patients with proven mutations in genes of the RAS/MAPK signaling pathway

European Human Genetics Conference 2010

Debora Romeo BERTOLA; A S BRASIL; Alexander A L JORGE; A C MALAQUIAS; Luciana T WANDERLEY et al

2010 Trabalho em evento
LS Genetics

High frequency of autistic traits in Williams-beuren patients

European Human Genetics Conference 2010

Chong Ae KIM; Francisco B Assumpção JUNIOR; Rachel Sayuri HONJO; Roberta Lelis DUTRA; Vera A S AMARAL et al

2010 Trabalho em evento
LS Genetics

Mechanisms of Ring Chromosome Formation

European Human Genetics Conference 2010

Maria Isabel MELARAGNO; V A F MELONI; Chong Ae KIM; Rachel Sayuri HONJO; D M CHRISTOFOLINI et al

2010 Trabalho em evento
LS Genetics

First Brazilian Case of Lysinuric Protein Intolerance (LPI)

European Human Genetics Conference 2010

Isabel Mosca FURQUIM; Rachel Sayuri HONJO; C M LOURENÇO; T MAUAD; D R BERTOLA et al

2010 Trabalho em evento
HS Genetics (clinical)

Enzyme replacement therapy in 25 mucopolyssaccharidosis type VI Brazilian children under five years

11th International Symposium on Mucopolysaccharide and related diseases

Dafne HOROVITZ; T P C MAGALHÃES; A ACOSTA; E M RIBEIRO; L GIUGLIANI et al

2010 Trabalho em evento
HS Pediatrics; Perinatology and Child Health

Replacement therapy in mucopolysaccharidosis typi VI: Advantages of early onset of treatment regarding cardiac involvement

11th International Symposium on Mucopolysaccharide and related disease

G N LEAL; Ana Carolina PAULA; Chong Ae KIM

2010 Trabalho em evento
LS Genetics

Genotype-phenotype delineation of terminal deletions 18q demonstrating high phenotypic variability

European Human Genetics Conference 2010

L D KULIKOWSKI; M YOSHIMOTO; C M MONMA; F T S BELLUCCO; S I N BELANGERO et al

2010 Artigo em periódico
HS Psychiatry and Mental Health

Alterações comportamentais na Síndrome de Noonan: dados preliminares brasileiros.

Revista Latinoamericana de Psicología

Erica R MOTA; D R BERTOLA; Chong Ae KIM; Maria Cristina T V TEIXEIRA

ISSN 0120-0534
2010 Artigo em periódico
LS Genetics

Williams-Beuren syndrome:Diagnosis by polymorphic markers

Genetic Testing

Ivanete Chaves SBRUZZI; A C PEREIRA; Beatriz VASCONCELOS; Rachel Sayuri HONJO; J E KRIEGER et al

ISSN 1090-6576
2010 Artigo em periódico
SH Psychology (miscellaneous)

Fenótipo comportamental de crianças e adolescentes com síndrome de Prader-Willi

Revista Paulista de Pediatria (Impresso)

Maria Luiza G De MESQUITA; Decio BRUNONI; João Monteiro De Pina NETO; Chong Ae KIM; Márcia Helena S MELO et al

ISSN 0103-0582
2010 Artigo em periódico
HS Medicine (miscellaneous)

Echocardiographic study of paediatric patients with mucopolycaccharidosis

Cardiology in the Young

G N LEAL; Ana Carolina PAULA; C LEONE; Chong Ae KIM

ISSN 1047-9511
2010 Artigo em periódico
LS Genetics

PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-like syndromes

Genetic Testing

A S BRASIL; A C PEREIRA; Luciana T WANDERLEY; Chong Ae KIM; A C MALAQUIAS et al

ISSN 1090-6576
2010 Artigo em periódico
HS Genetics (clinical)

Craniosynostosis in Pycnodysostosis: Broading the Spectrum of the Cranial Flat Bone Abnormalities

American Journal of Medical Genetics. Part A

Debora Romeo BERTOLA; Cassio AMARAL; Chong Ae KIM; L M J ALBANO; Meire AGUENA et al

ISSN 1552-4825
2010 Artigo em periódico
HS Medicine (miscellaneous)

DiGeorge syndrome: a not so rare syndrome

Clinics (USP. Impresso)

A B F FOMIN; A C PASTORINO; Chong Ae KIM; A C PEREIRA; M Carneiro SAMPAIO et al

ISSN 1807-5932
2010 Artigo em periódico
HS Genetics (clinical)

Enzyme replacement the therapy fro mucopolysaccharidoses: I;II and VI: recommendation from a group of brazilian F experts

Revista da Associação Médica Brasileira (1992. Impresso)

Roberto GIUGLIANI; A FEDERHEN; M V MUNOZ; T A VIEIRA; O ARTIGALÁS et al

ISSN 0104-4230
2010 Artigo em periódico
LS Neurology

Two Distinct Regions in 2q24.2-q24.3 Associated with Idiopathic Epilepsy

Epilepsia (Copenhagen)

A C Krepischi SANTOS; J KNIJNENBURG; D R BEROLA; Chong Ae KIM; P L PEARSON et al

ISSN 0013-9580
2010 Artigo em periódico
SH Psychology (miscellaneous)

Behavioral and cognitive phenotype of children and adolescent with Williams-Beuren syndrome

Pró-Fono (Impresso)

Maria Cristina T V TEIXEIRA; Camila Rondinelli Cobra MONTEIRO; Renata De Lima VELLOSO; Chong Ae KIM; Luiz Renato Rodrigues CARREIRO

ISSN 0104-5687
2010 Artigo em periódico
LS Molecular Biology

All Ilustrative Case of Neurofibromatosis type 1 and NF1Microdeletion

Molecular Syndromology

L A PRAXEDES; F M PEREIRA; Juliana MAZZEU; S S COSTA; Debora Romeo BERTOLA et al

ISSN 1661-8769
2010 Artigo em periódico
HS Endocrinology; Diabetes and Metabolism

Co-ocurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?

Arquivos Brasileiros de Endocrinologia e Metabologia (Impresso)

A S BRASIL; Chong Ae KIM; J KRIEGER; A C PEREIRA; Debora Romeo BERTOLA

ISSN 0004-2730
2010 Artigo em periódico
HS Genetics (clinical)

Obesity in Pycnodisostosis due to UPD1: Possible effect of an Imprinted gene in Chromosome 1

American Journal of Medical Genetics. Part A

Debora Romeo BERTOLA; Meire AGUENA; G L YAMAMOTO; Chong Ae KIM; M R Passo BUENO

ISSN 1552-4825