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
2005 Trabalho em evento
Síndrome do cromossomo em anel B VASCONCELOS; I C SBRUZZI; L M J ALBANO; D R BERTOLA; C P KOIFFMANN et al XVII Congresso Nacional de Genética Clínica
LS Genetics
2005 Trabalho em evento
Síndrome da aorta - relato de caso S ZANINI; Gustavo D COELHO; E A FURUSAWA; L SUZUKI; Chong Ae KIM et al XIII Congresso Brasileiro de Nefrologia Pediátrica
SH Psychology (miscellaneous)
2005 Trabalho em evento
MPS-brazil Network: a country wide iniciative to improve diagnosis and management of mucopolysaccharidoses in Brazil I SCHWATZ; K SOEIRO; C RAFAELLI; M BURIN; J COELHO et al 5th International Symposium on Lysosomal Storage Diseases
HS Infectious Diseases
2005 Trabalho em evento
Clinical follow up of the five patients with Rothmund Thomson: Importance of osteosarcoma Claudia Renata Leite SILVA; D R BERTOLA; L M J ALBANO; Vicente Odone FILHO; Chong Ae KIM 55th Annual Meeting of the American Society of Human Genetics
HS Neurology (clinical)
2005 Trabalho em evento
Clinical study of the five patients with trichorhinophalangeal syndrome L M J ALBANO; Tatiana B BRASIL; M B MOREIRA; Claudia Renata Leite SILVA; D R BERTOLA et al 55th Annual Meeting of the American Society of Human Genetics
LS Genetics
2005 Trabalho em evento
Prader-Willi-like phenotype: Investigation of 1p36 deletion in 41 patients with delayed psychomotor development; hypotonia; obesity and/or hyperphagia; learning disabilities and behavioral problems. C S D ANGELO; J A PAZ; Chong Ae KIM; D R BERTOLA; C I E CASTRO et al 55th Annual Meeting of the American Society of Human Genetics
HS Pediatrics; Perinatology and Child Health
2005 Trabalho em evento
CKN1 gene analysis in Cockayne syndrome: novel mutaion in eight typical patients Debora Romeo BERTOLA; Hernian CAO; L M J ALBANO; Daniela P OLIVEIRA; F KOK et al 55th Annual Meeting of the American Society of Human Genetics
LS Genetics
2005 Trabalho em evento
A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity. M C VARELA; Chong Ae KIM; Debora Romeo BERTOLA; A Y Simões SATO; C I E C FABRIS et al 55th Annual Meeting of the American Society of Human Genetics
HS Neurology (clinical)
2005 Trabalho em evento
Ring chromosome syndrome: report of 12 cases B VASCONCELOS; L M J ALBANO; C I E CASTRO; Debora Romeo BERTOLA; I C SBRUZZI et al 55th Annual Meeting of the American Society of Human Genetics
LS Genetics
2005 Artigo em periódico
Impact of molecular mechanisms; including deletion size; on Prader-Willi syndrome phenotype: study of 75 patients. M C VARELA; F KOK; N SETIAN; Chong Ae KIM; C P KOIFFMANN Clinical Genetics ISSN 0009-9163
HS Neurology (clinical)
2005 Artigo em periódico
O pediatra e o aconselhamento genético Chong Ae KIM Pediatria (USP) ISSN 0101-3858
SH Education
2005 Artigo em periódico
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. F S JEHEE; D JOHNSON; L ALONSO; D P CAVALCANTI; E De Sá MOREIRA et al Clinical Genetics ISSN 0009-9163
LS Clinical Biochemistry
2005 Artigo em periódico
Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome Minrong AI; Shauna HEEGER; Cynthia F BARTELS; Deborah K SCHELLING; Konrad OEXLE et al American Journal of Human Genetics ISSN 0002-9297
HS Pediatrics; Perinatology and Child Health
2005 Artigo em periódico
CHILD Syndrome Caused by a deletion of Exons 6-8 of the NSDHL Gene Chong Ae KIM; A KÖNIG; D R BEROLA; L M J ALBANO; G J F GATTÁS et al Dermatology (Basel) ISSN 1018-8665
LS Genetics
2005 Artigo em periódico
Neurofibromatosis-Noonan Syndrome: Molecular Evidence of the Concurrence of Both Disorders in a Patient Debora R BERTOLA; Alexandre C PEREIRA; Fabio PASSETTI; Paulo S L De OLIVEIRA; Ludwine MESSIAEN et al American Journal of Medical Genetics. Part A ISSN 1552-4825
HS Genetics (clinical)
2005 Artigo em periódico
Mucopolysaccharidosis type VI:Identification of novel mutations on the arylsulphatase B gene in South American patients M F G PETRY; K NONEMACHER; J C SEBBEN; I V D SCHWARTZ; A C M AZEVEDO et al Journal of Inherited Metabolic Disease ISSN 0141-8955
LS Genetics
2004 Capítulo de livro
Abordagem Prática do Paciente com Malformação Congênita Chong Ae KIM; Denise DERANI Manual do Residente de Pediatria
HS Pediatrics; Perinatology and Child Health
2004 Capítulo de livro
Aconselhamento Genético Chong Ae KIM; Denise DERANI Manual do Médico Residente de Pediatria
HS Genetics (clinical)
2004 Trabalho em evento
Galactosialidose: relato de tres casos com início precoce L M J ALBANO; M SANO; L YANO; E M A DINIZ; D R BERTOLA et al XVI Congresso Brasileiro de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Omodisplasia: Relato do primeiro caso brasileiro L Mj ALBANO; L A N OLIVEIRA; D R BERTOLA; A C PAULA; T P DELBONI et al XVI Congresso Brasileiro de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Achados radiológicos em pacientes com Mucopolissacaridose A C PAULA; A C G M SANTOS; T P DELBONI; D R BERTOLA; L M J ALBANO et al XVI Congresso Brasileiro de Genética Clínica
HS Radiology; Nuclear Medicine and Imaging
2004 Trabalho em evento
Mucopolissacaridose tipo VI - Estudo de correlação genótipo-fenótipo em seis brasileiros portadores da mutação I533del23 A C AZEVEDO; I V SCHWARTZ; M PETRY; A P BEHEREGARAY; F T SOUZA et al XVI Congresso Brasileiro de Genética Clínica
HS Genetics (clinical)
2004 Trabalho em evento
Further evidence that the T731 PTPN11 gene mutation is associated with myeloproliferative disorder in Noonan syndrome D R BERTOLA; A C PEREIRA; J D A CARNEIRO; J E KRIEGER; Chong Ae KIM Annual Clinical Genetics Meeting
HS Genetics (clinical)
2004 Trabalho em evento
Achados radiológicos em pacientes com Mucopolissacaridose tipo VI (Síndrome de Maroteaux-Lamy) A C PAULA; F Donato JR; D R BERTOLA; L M J ALBANO; Chong Ae KIM et al 34ª Jornada Paulista de Radiologia
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 D R BERTOLA; A C PEREIRA; J D A CARNEIRO; J KRIEGER; Chong Ae KIM Annual Clinical Genetics Meeting. American College of Medical Genetics
HS Genetics (clinical)
2005 Trabalho em evento
LS Genetics

Síndrome do cromossomo em anel

XVII Congresso Nacional de Genética Clínica

B VASCONCELOS; I C SBRUZZI; L M J ALBANO; D R BERTOLA; C P KOIFFMANN et al

2005 Trabalho em evento
SH Psychology (miscellaneous)

Síndrome da aorta - relato de caso

XIII Congresso Brasileiro de Nefrologia Pediátrica

S ZANINI; Gustavo D COELHO; E A FURUSAWA; L SUZUKI; Chong Ae KIM et al

2005 Trabalho em evento
HS Infectious Diseases

MPS-brazil Network: a country wide iniciative to improve diagnosis and management of mucopolysaccharidoses in Brazil

5th International Symposium on Lysosomal Storage Diseases

I SCHWATZ; K SOEIRO; C RAFAELLI; M BURIN; J COELHO et al

2005 Trabalho em evento
HS Neurology (clinical)

Clinical follow up of the five patients with Rothmund Thomson: Importance of osteosarcoma

55th Annual Meeting of the American Society of Human Genetics

Claudia Renata Leite SILVA; D R BERTOLA; L M J ALBANO; Vicente Odone FILHO; Chong Ae KIM

2005 Trabalho em evento
LS Genetics

Clinical study of the five patients with trichorhinophalangeal syndrome

55th Annual Meeting of the American Society of Human Genetics

L M J ALBANO; Tatiana B BRASIL; M B MOREIRA; Claudia Renata Leite SILVA; D R BERTOLA et al

2005 Trabalho em evento
HS Pediatrics; Perinatology and Child Health

Prader-Willi-like phenotype: Investigation of 1p36 deletion in 41 patients with delayed psychomotor development; hypotonia; obesity and/or hyperphagia; learning disabilities and behavioral problems.

55th Annual Meeting of the American Society of Human Genetics

C S D ANGELO; J A PAZ; Chong Ae KIM; D R BERTOLA; C I E CASTRO et al

2005 Trabalho em evento
LS Genetics

CKN1 gene analysis in Cockayne syndrome: novel mutaion in eight typical patients

55th Annual Meeting of the American Society of Human Genetics

Debora Romeo BERTOLA; Hernian CAO; L M J ALBANO; Daniela P OLIVEIRA; F KOK et al

2005 Trabalho em evento
HS Neurology (clinical)

A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.

55th Annual Meeting of the American Society of Human Genetics

M C VARELA; Chong Ae KIM; Debora Romeo BERTOLA; A Y Simões SATO; C I E C FABRIS et al

2005 Trabalho em evento
LS Genetics

Ring chromosome syndrome: report of 12 cases

55th Annual Meeting of the American Society of Human Genetics

B VASCONCELOS; L M J ALBANO; C I E CASTRO; Debora Romeo BERTOLA; I C SBRUZZI et al

2005 Artigo em periódico
HS Neurology (clinical)

Impact of molecular mechanisms; including deletion size; on Prader-Willi syndrome phenotype: study of 75 patients.

Clinical Genetics

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

ISSN 0009-9163
2005 Artigo em periódico
SH Education

O pediatra e o aconselhamento genético

Pediatria (USP)

Chong Ae KIM

ISSN 0101-3858
2005 Artigo em periódico
LS Clinical Biochemistry

Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.

Clinical Genetics

F S JEHEE; D JOHNSON; L ALONSO; D P CAVALCANTI; E De Sá MOREIRA et al

ISSN 0009-9163
2005 Artigo em periódico
HS Pediatrics; Perinatology and Child Health

Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome

American Journal of Human Genetics

Minrong AI; Shauna HEEGER; Cynthia F BARTELS; Deborah K SCHELLING; Konrad OEXLE et al

ISSN 0002-9297
2005 Artigo em periódico
LS Genetics

CHILD Syndrome Caused by a deletion of Exons 6-8 of the NSDHL Gene

Dermatology (Basel)

Chong Ae KIM; A KÖNIG; D R BEROLA; L M J ALBANO; G J F GATTÁS et al

ISSN 1018-8665
2005 Artigo em periódico
HS Genetics (clinical)

Neurofibromatosis-Noonan Syndrome: Molecular Evidence of the Concurrence of Both Disorders in a Patient

American Journal of Medical Genetics. Part A

Debora R BERTOLA; Alexandre C PEREIRA; Fabio PASSETTI; Paulo S L De OLIVEIRA; Ludwine MESSIAEN et al

ISSN 1552-4825
2005 Artigo em periódico
LS Genetics

Mucopolysaccharidosis type VI:Identification of novel mutations on the arylsulphatase B gene in South American patients

Journal of Inherited Metabolic Disease

M F G PETRY; K NONEMACHER; J C SEBBEN; I V D SCHWARTZ; A C M AZEVEDO et al

ISSN 0141-8955
2004 Capítulo de livro
HS Pediatrics; Perinatology and Child Health

Abordagem Prática do Paciente com Malformação Congênita

Manual do Residente de Pediatria

Chong Ae KIM; Denise DERANI

2004 Capítulo de livro
HS Genetics (clinical)

Aconselhamento Genético

Manual do Médico Residente de Pediatria

Chong Ae KIM; Denise DERANI

2004 Trabalho em evento
HS Genetics (clinical)

Galactosialidose: relato de tres casos com início precoce

XVI Congresso Brasileiro de Genética Clínica

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

2004 Trabalho em evento
HS Genetics (clinical)

Omodisplasia: Relato do primeiro caso brasileiro

XVI Congresso Brasileiro de Genética Clínica

L Mj 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 Brasileiro de Genética Clínica

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

2004 Trabalho em evento
HS Genetics (clinical)

Mucopolissacaridose tipo VI - Estudo de correlação genótipo-fenótipo em seis brasileiros portadores da mutação I533del23

XVI Congresso Brasileiro de Genética Clínica

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

2004 Trabalho em evento
HS Genetics (clinical)

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

Annual Clinical Genetics Meeting

D R BERTOLA; A C PEREIRA; J D A CARNEIRO; J E KRIEGER; Chong Ae KIM

2004 Trabalho em evento
HS Radiology; Nuclear Medicine and Imaging

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

34ª Jornada Paulista de Radiologia

A C PAULA; F Donato JR; D R BERTOLA; L M J ALBANO; Chong Ae KIM et al

2004 Trabalho em evento
HS Genetics (clinical)

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

Annual Clinical Genetics Meeting. American College of Medical Genetics

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