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
2008 Artigo em periódico
Genetic and clinical aspects of neurofibromatosis type I:study of a large sample of affected Brazilian individuals. L A PRAXEDES; Jenneke Van Den ENDE; Yolande Van BEVER; Chong Ae KIM; P A OTTO RBM. Revista Brasileira de Medicina (Rio de Janeiro) ISSN 0034-7264
HS Genetics (clinical)
2008 Artigo em periódico
Trissomia; tetrassomia e pentassomia do cromossomo X: relato de 11 casos. B VASCONCELOS; S ANTONINI; L M J ALBANO; D R BERTOLA; Rachel Sayuri HONJO et al Pediatria (USP) ISSN 0101-3858
LS Genetics
2007 Capítulo de livro
Síndromes associadas à obesidade Chong Ae KIM; L M J ALBANO; Debora Romeo BERTOLA Obesidade na Criança e no Adolescente ISBN 978-85-7241-7
HS Pediatrics; Perinatology and Child Health
2007 Trabalho em evento
Hepatic involvement in Cockayne syndrome type A D R BERTOLA; G PORTA; M P GONÇALVES; S R CARDOSO; L SUZUKI et al European Human Genetics Conference
HS Pediatrics; Perinatology and Child Health
2007 Trabalho em evento
Otopalatodigital type I syndrome: report of a familial case. L M J ALBANO; S P ROBERTSON; L A N OLIVEIRA; D R BERTOLA; Chong Ae KIM European Human Genetics Conference
HS Radiology; Nuclear Medicine and Imaging
2007 Trabalho em evento
SOST gene mutation in two Brazilian families with sclerosteosis. Chong Ae KIM; R HONJO; D R BERTOLA; L M J ALBANO; L A N OLIVEIRA et al Eurpean Human Genetics Conference
LS Genetics
2007 Trabalho em evento
SOST gene mutation in two Brazilian families with sclerosteosis Chong Ae KIM; R HONJO; Debora Romeo BERTOLA; L M J ALBANO; L A N OLIVEIRA et al European Human Genetics Conference
LS Genetics
2007 Trabalho em evento
Alert to asymptomatic arteial hypertension in Williams-Beuren syndrome in childhood R HONJO; E A FURASAWA; D R BERTOLA; L M J ALBANO; L SUZUKI et al 57th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2007 Trabalho em evento
Cleidocranial dysplasia: the use of a specific protocol to detect atypical cases and new findings in eight Brazilian cases J P G PEREIRA; L A N OLIVEIRA; Debora Romeo BERTOLA; R HONJO; Chong Ae KIM et al 57th Annual Meeting of the American Society of Human Genetics
LS Neurology
2007 Trabalho em evento
Dental evaluation of kabuki syndrome patients C S TEIXEIRA; Claudia Renata Leite SILVA; Rachel Sayuri HONJO; D R BEROLA; L M J ALBANO et al 57th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2007 Trabalho em evento
Importance of dental anomalies to the dignosis of Smith-Magenis syndrome: description of two cases Claudia Renata Leite SILVA; C S TEIXEIRA; Rachel Sayuri HONJO; Debora Romeo BERTOLA; L M J ALBANO et al 57th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2007 Trabalho em evento
KRAS gene mutation analysis in a cohort of 50 Brazilian patients with Noonan and Noonan-like syndromes D R BEROLA; Debora Romeo BERTOLA; A S BRASIL; A C PEREIRA; L M J ALBANO et al 57th Annual Meeting of the American Society of Human Genetics
HS Genetics (clinical)
2007 Trabalho em evento
Angiokeratoma: an important clue for the diagnosis of Fabry disease L M J ALBANO; M C RIVITTI; R GIUGLIANI; L C F SÁ; Debora Romeo BERTOLA et al 57th Annual Meeting of the American Society of Human Genetics
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)
2007 Trabalho em evento
Significance of submicroscopic genomic imbalances in mental retardation A C Krepischi SANTOS; A M MORGANTE; F KOK; Chong Ae KIM; P A OTTO et al 57th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2007 Trabalho em evento
Investigation of 300 patients with delayed psicomotor development; obesity; hyperphagia; learning disabilities and behavioral problems M C VARELA; C S D ANGELO; I KOHL; C I E CASTRO; F KOK et al 57th Annual Meeting of the American Society of Human Genetics
HS Medicine (miscellaneous)
2007 Trabalho em evento
Prevalence of autism spectrum disorders in patients with Möbius sequence E KLUCZINK; Chong Ae KIM; C H GONZALEZ; J A PAZ; Maria Joaquina Marques DIAS 57th Annual Meeting of the American Society of Human Genetics
LS Neuroscience (miscellaneous)
2007 Trabalho em evento
Hipertensão Arterial na Mucopolissacaridose Ana Carolina De PAULA; V H KOCH; E A FURASAWA; G MOREIRA; Chong Ae KIM XII Simposio Latinoamericano de Enfermidades de Depósito Lisosomal
HS Medicine (miscellaneous)
2007 Trabalho em evento
Acompanhamento clínico de 30 pacientes com mucopolissacaridoses Ana Carolina PAULA; G N LEAL; L M J ALBANO; Debora Romeo BERTOLA; Rachel Sayuri HONJO et al I Congreso Latinoamericano de Enfermedades Lisosomales
HS Genetics (clinical)
2007 Trabalho em evento
Achados radiológicos em 30 pacientes com mucopolissacaridoses Ana Carolina PAULA; L A N OLIVEIRA; M CARVALHO; L M J ALBANO; Debora Romeo BERTOLA et al I Congreso Latinoamericano de Enfermedades Lisosomales
LS Genetics
2007 Trabalho em evento
The long path from birth until diagnosis: a study in 113 brazilian patients with mucopolysacharidoses T A VIEIRA; I V SCHWARTZ; M V MUNOZ; L L PINTO; C E STEINER et al I Congreso Latinoamericano de Enfermedades Lisosomales
HS Medicine (miscellaneous)
2007 Trabalho em evento
The Hunter outcome survey: data on Latin American patients and preliminary comparison data from the rest of the world R GIUGLIANI; L PINTO; T A VIEIRA; M V MUNOZ; I V SCHWARTZ et al I Congreso Latinoamericano de Enfermedades Lisosomales
HS Medicine (miscellaneous)
2007 Artigo em periódico
Phenotypic overlap in Melnick-Needles;serpentine fibula-polycystic kidney and Hajdu-Cheney syndrome:a clinical and molecular study in three patients. L M J ALBANO; Debora Romeo BERTOLA; M F BARBA; M VALENTE; S P ROBERTSON et al Clinical Dysmorphology ISSN 0962-8827
LS Molecular Biology
2007 Artigo em periódico
SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability Alexander A L JORGE; Silvia C SOUZA; Mirian Y NISHI; Billerbeck A E; Debora C C LIBORIO et al Clinical Endocrinology (Oxford) ISSN 0300-0664
LS Endocrinology
2007 Artigo em periódico
A clinical study of 77 patients with mucopolysaccharidosis type II I V SCHWARTZ; M RIBEIRO; J MOTA; Maria Betania P TORALLES; P CORREIA et al Acta Paediatrica (Oslo) ISSN 0803-5253
HS Pediatrics; Perinatology and Child Health
2007 Artigo em periódico
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB. L S BICKNELL; C Farrington ROCK; Y SCHAFEGHATI; Y ALEMBIK; N Al MADANI et al Journal of Medical Genetics ISSN 0022-2593
LS Genetics
2008 Artigo em periódico
HS Genetics (clinical)

Genetic and clinical aspects of neurofibromatosis type I:study of a large sample of affected Brazilian individuals.

RBM. Revista Brasileira de Medicina (Rio de Janeiro)

L A PRAXEDES; Jenneke Van Den ENDE; Yolande Van BEVER; Chong Ae KIM; P A OTTO

ISSN 0034-7264
2008 Artigo em periódico
LS Genetics

Trissomia; tetrassomia e pentassomia do cromossomo X: relato de 11 casos.

Pediatria (USP)

B VASCONCELOS; S ANTONINI; L M J ALBANO; D R BERTOLA; Rachel Sayuri HONJO et al

ISSN 0101-3858
2007 Capítulo de livro
HS Pediatrics; Perinatology and Child Health

Síndromes associadas à obesidade

Obesidade na Criança e no Adolescente

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

ISBN 978-85-7241-7
2007 Trabalho em evento
HS Pediatrics; Perinatology and Child Health

Hepatic involvement in Cockayne syndrome type A

European Human Genetics Conference

D R BERTOLA; G PORTA; M P GONÇALVES; S R CARDOSO; L SUZUKI et al

2007 Trabalho em evento
HS Radiology; Nuclear Medicine and Imaging

Otopalatodigital type I syndrome: report of a familial case.

European Human Genetics Conference

L M J ALBANO; S P ROBERTSON; L A N OLIVEIRA; D R BERTOLA; Chong Ae KIM

2007 Trabalho em evento
LS Genetics

SOST gene mutation in two Brazilian families with sclerosteosis.

Eurpean Human Genetics Conference

Chong Ae KIM; R HONJO; D R BERTOLA; L M J ALBANO; L A N OLIVEIRA et al

2007 Trabalho em evento
LS Genetics

SOST gene mutation in two Brazilian families with sclerosteosis

European Human Genetics Conference

Chong Ae KIM; R HONJO; Debora Romeo BERTOLA; L M J ALBANO; L A N OLIVEIRA et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

Alert to asymptomatic arteial hypertension in Williams-Beuren syndrome in childhood

57th Annual Meeting of the American Society of Human Genetics

R HONJO; E A FURASAWA; D R BERTOLA; L M J ALBANO; L SUZUKI et al

2007 Trabalho em evento
LS Neurology

Cleidocranial dysplasia: the use of a specific protocol to detect atypical cases and new findings in eight Brazilian cases

57th Annual Meeting of the American Society of Human Genetics

J P G PEREIRA; L A N OLIVEIRA; Debora Romeo BERTOLA; R HONJO; Chong Ae KIM et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

Dental evaluation of kabuki syndrome patients

57th Annual Meeting of the American Society of Human Genetics

C S TEIXEIRA; Claudia Renata Leite SILVA; Rachel Sayuri HONJO; D R BEROLA; L M J ALBANO et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

Importance of dental anomalies to the dignosis of Smith-Magenis syndrome: description of two cases

57th Annual Meeting of the American Society of Human Genetics

Claudia Renata Leite SILVA; C S TEIXEIRA; Rachel Sayuri HONJO; Debora Romeo BERTOLA; L M J ALBANO et al

2007 Trabalho em evento
HS Genetics (clinical)

KRAS gene mutation analysis in a cohort of 50 Brazilian patients with Noonan and Noonan-like syndromes

57th Annual Meeting of the American Society of Human Genetics

D R BEROLA; Debora Romeo BERTOLA; A S BRASIL; A C PEREIRA; L M J ALBANO et al

2007 Trabalho em evento
LS Biochemistry; Genetics and Molecular Biology (miscellaneous)

Angiokeratoma: an important clue for the diagnosis of Fabry disease

57th Annual Meeting of the American Society of Human Genetics

L M J ALBANO; M C RIVITTI; R GIUGLIANI; L C F SÁ; Debora Romeo BERTOLA et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

Significance of submicroscopic genomic imbalances in mental retardation

57th Annual Meeting of the American Society of Human Genetics

A C Krepischi SANTOS; A M MORGANTE; F KOK; Chong Ae KIM; P A OTTO et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

Investigation of 300 patients with delayed psicomotor development; obesity; hyperphagia; learning disabilities and behavioral problems

57th Annual Meeting of the American Society of Human Genetics

M C VARELA; C S D ANGELO; I KOHL; C I E CASTRO; F KOK et al

2007 Trabalho em evento
LS Neuroscience (miscellaneous)

Prevalence of autism spectrum disorders in patients with Möbius sequence

57th Annual Meeting of the American Society of Human Genetics

E KLUCZINK; Chong Ae KIM; C H GONZALEZ; J A PAZ; Maria Joaquina Marques DIAS

2007 Trabalho em evento
HS Medicine (miscellaneous)

Hipertensão Arterial na Mucopolissacaridose

XII Simposio Latinoamericano de Enfermidades de Depósito Lisosomal

Ana Carolina De PAULA; V H KOCH; E A FURASAWA; G MOREIRA; Chong Ae KIM

2007 Trabalho em evento
HS Genetics (clinical)

Acompanhamento clínico de 30 pacientes com mucopolissacaridoses

I Congreso Latinoamericano de Enfermedades Lisosomales

Ana Carolina PAULA; G N LEAL; L M J ALBANO; Debora Romeo BERTOLA; Rachel Sayuri HONJO et al

2007 Trabalho em evento
LS Genetics

Achados radiológicos em 30 pacientes com mucopolissacaridoses

I Congreso Latinoamericano de Enfermedades Lisosomales

Ana Carolina PAULA; L A N OLIVEIRA; M CARVALHO; L M J ALBANO; Debora Romeo BERTOLA et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

The long path from birth until diagnosis: a study in 113 brazilian patients with mucopolysacharidoses

I Congreso Latinoamericano de Enfermedades Lisosomales

T A VIEIRA; I V SCHWARTZ; M V MUNOZ; L L PINTO; C E STEINER et al

2007 Trabalho em evento
HS Medicine (miscellaneous)

The Hunter outcome survey: data on Latin American patients and preliminary comparison data from the rest of the world

I Congreso Latinoamericano de Enfermedades Lisosomales

R GIUGLIANI; L PINTO; T A VIEIRA; M V MUNOZ; I V SCHWARTZ et al

2007 Artigo em periódico
LS Molecular Biology

Phenotypic overlap in Melnick-Needles;serpentine fibula-polycystic kidney and Hajdu-Cheney syndrome:a clinical and molecular study in three patients.

Clinical Dysmorphology

L M J ALBANO; Debora Romeo BERTOLA; M F BARBA; M VALENTE; S P ROBERTSON et al

ISSN 0962-8827
2007 Artigo em periódico
LS Endocrinology

SHOX mutations in idiopathic short stature and Leri-Weill dyschondrosteosis: frequency and phenotypic variability

Clinical Endocrinology (Oxford)

Alexander A L JORGE; Silvia C SOUZA; Mirian Y NISHI; Billerbeck A E; Debora C C LIBORIO et al

ISSN 0300-0664
2007 Artigo em periódico
HS Pediatrics; Perinatology and Child Health

A clinical study of 77 patients with mucopolysaccharidosis type II

Acta Paediatrica (Oslo)

I V SCHWARTZ; M RIBEIRO; J MOTA; Maria Betania P TORALLES; P CORREIA et al

ISSN 0803-5253
2007 Artigo em periódico
LS Genetics

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Journal of Medical Genetics

L S BICKNELL; C Farrington ROCK; Y SCHAFEGHATI; Y ALEMBIK; N Al MADANI et al

ISSN 0022-2593