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
1999 Trabalho em evento
Analysis of the 677C - T polymorphism in the methylenetetrahydrofolate reductase gene as a risk factor to neural tube defects. A L A CUNHA; M H HIRATA; Chong Ae KIM; S T SANTOS; R D C HIRATA Congressso de Patologia e Medicina Laboratorial. 33º Brasileiro- 4º Mercosul- 20º Mundial- 3º Gestão Laboratorial
HS Pediatrics; Perinatology and Child Health
1999 Trabalho em evento
Cromossomo 4 em anel: estrutura e correlação genótipo-fenótipo C I E CASTRO; D R BERTOLA; S M M SUGAYAMA; Chong Ae KIM; C P KOIFFMANN 45º Congresso Nacional de Genética ISBN 14154757
LS Genetics
1999 Trabalho em evento
Dissomia uniparenteral como causa de doença genética S A S FONSECA; C L BOROVICK; R MULLER; Chong Ae KIM; A M MORGANTE 45º Congresso Nacional de Genética ISBN 14154757
LS Genetics
1999 Trabalho em evento
Estudo genético-clínico e molecular da neurofibromatose L A PRAXEDES; R C Migroni NETO; P A OTTO; Chong Ae KIM; F ARITA 45º Congresso Nacional de Genética ISBN 14154757
HS Genetics (clinical)
1999 Trabalho em evento
Análise molecular de deleções 4p associadas com a síndrome de Wolf-Hirschhorn E P P SILVA; Chong Ae KIM; S M M SUGAYAMA; C Y UTAGAWA; C P KOIFFMANN 45º Congresso Nacional de Genética ISBN 14154757
LS Genetics
1999 Trabalho em evento
Estudo dos sinais clínicos e relevância no diagnóstico da neurofibromatose L A PRAXEDES; R C Migroni NETO; P A OTTO; Chong Ae KIM; F ARITA 45º Congresso Nacional de Genética ISBN 14154757
HS Genetics (clinical)
1999 Trabalho em evento
Síndrome de Pallister-Killian: detecção do i (12p) por Fish em mucosa oral C L BOROVICK; E Auler BITENCOURT; A P M SILVA; Chong Ae KIM; S M M SUGAYAMA et al 45º Congresso Nacional de Genética ISBN 14154757
LS Genetics
1999 Trabalho em evento
Triagem de mutações no gene CFTR em 160 pacientes com fibrose cística do pâncreas A BERNADINO; A FERRI; M R Passos BUENO; Chong Ae KIM; C M A NAKAIE et al 45º Congresso Nacional de Genética ISBN 14154757
HS Genetics (clinical)
1999 Trabalho em evento
Estudo da mutação R 334W em sete pacientes com fibrose cística do pâncreas K E MIRANDA; A L BERNARDINO; A FERRI; M R Passo BUENO; C M A NAKAIE et al 45º Congresso Nacional de Genética ISBN 14154757
LS Genetics
1999 Trabalho em evento
The gene for the camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) encodes a secreted proteoglycan that in essential to normal joint function J MARCELINO; J D CARPTEM; W M SUWAIRI; S SCHWARTZ; C ROBBINS et al Annual Meeting. The American Society of Human Genetics
LS Genetics
1999 Trabalho em evento
Noonan syndrome: a clinical and genetic study of 31 patients D R BEROLA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; L M J ALBANO; J D A CARNEIRO et al Annual Meeting. The American Society of Human Genetics
HS Genetics (clinical)
1999 Trabalho em evento
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations A L BERNARDINO; A FERRI; M R Passo BUENO; Chong Ae KIM; C M A NAKAIE et al Annual Meeting. The American Society of Human Genetics
LS Genetics
1999 Trabalho em evento
Clinical study and use of FISH analysis to diagnostic approach of Brazilian patients with Williams-Beuren syndrome Sofia Mizuko Miura SUGAYAMA; M L F CHAUFFAILLE; C J ABE; D R BEROLA; L ALBANO et al Annual Meeting of the American Society of Human Genetics
HS Genetics (clinical)
1999 Trabalho em evento
Dysostosis spondylocosital: a clinical study of 14 patients S M M UTAGAWA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; Debora Romeo BERTOLA; L A N OLIVEIRA et al Annual Meeting. The American Society of Human Genetics
HS Embryology
1999 Trabalho em evento
Dilemma to chronic ventilation in Werdnig-Hoffmann disease: study of 15 patients Chong Ae KIM; P LECUSSAN; E B CASELLA; M J ALBANO; G OSELKA Annual Meeting. The American Society of Human Genetics
HS Genetics (clinical)
1999 Trabalho em evento
Estudo clínico-laboratorial de Mucopolissacaridoses: experiência de cinco anos L M J ALBANO; Sofia Mizuko Miura SUGAYAMA; Debora Romeo BERTOLA; Fávia PUPPI; C Y UTAGAWA et al XI Congresso Brasileiro de Genética Clínica
HS Genetics (clinical)
1999 Trabalho em evento
The gene for the camptodactily-arthropathy-coxa vara-pericarditis syndrome (CACP) encode a secreted proteoglycan that is essential to normal joint function J MARCELINO; J D CARPTEM; W M SUWAIRI; S SCHWARTZ; C ROBBINS et al 49th Annual Meeting. The American Society of Human Genetics
LS Genetics
1999 Trabalho em evento
Noonan syndrome: a clinical and genetic study of 31 patients Debora Romeo BERTOLA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; L M J ALBANO; J D A CARNEIRO et al 49th Annual Meeting. The American Society of Human Genetics
HS Genetics (clinical)
1999 Trabalho em evento
Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations A L F BENARDINO; A FERRI; M R Passos BUENO; Chong Ae KIM; C M A NAKAIE et al 49th Annual Meeting. The American Society of Human Genetics
HS Medicine (miscellaneous)
1999 Trabalho em evento
Clinical study and use of FISH analysis to diagnostic approach of brazilian patients with Williams-beuren syndrome Sofia Mizuko Miura SUGAYAMA; M L F CHAUFFAILLE; K T ABE; Debora Romeo BERTOLA; L M J ALBANO et al 49th Annual Meeting. The American Society of Human Genetics
LS Genetics
1999 Trabalho em evento
Dysostosis spondylocostal: a clinical study of 14 patients C Y UTAGAWA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; D R BERTOLA; L A N OLIVEIRA et al 49th Annual Meeting. The American Society of Human Genetics
HS Medicine (miscellaneous)
1999 Trabalho em evento
A clinical; cytogenetic and molecular study of three Brazilian patients with supernumerary Inv Dup(15) marker chromosomes. M C VARELA; C FRIDMAN; T E MATSUMOTO; Chong Ae KIM; F KOK et al 49th Annual Meeting. The American Society of Human Genetics
LS Genetics
1999 Trabalho em evento
Dilemma to chronic ventilation in Werdnig-Hoffmann disease: study of 16 patients Chong Ae KIM; P LECUSSAN; E B CASELLA; L M J ALBANO; G OSELKA 49th Annual Meeting. The American Society of Human Genetics
HS Medicine (miscellaneous)
1999 Trabalho em evento
Importance of cyanide-nitroprussiade test for the dianosis of homocystinuria Sofia Mizuko Miura SUGAYAMA; Chong Ae KIM; M M S K INOUE; C Y UTAGAWA; D R BERTOLA et al XX World Congress of Pathology/Laboratory Medicine; XXXIII Brazilian; IV Mercosul and the III Brazilian Congress of Laboratory Management
HS Neurology (clinical)
1999 Trabalho em evento
Use of FISH analysis to diagnostic approach of 11 Brazilian patients with Williams-Beuren syndrome S M M SUGAYAMA; Chong Ae KIM; K T ABE; L M J ALBANO; D R BERTOLA et al XX World Congress of Pathology/Laboratory Medicine; XXXIII Brazilian; IV Mercosul and the III Brazilian Congress of Laboratory Management
LS Neurology
1999 Trabalho em evento
HS Pediatrics; Perinatology and Child Health

Analysis of the 677C - T polymorphism in the methylenetetrahydrofolate reductase gene as a risk factor to neural tube defects.

Congressso de Patologia e Medicina Laboratorial. 33º Brasileiro- 4º Mercosul- 20º Mundial- 3º Gestão Laboratorial

A L A CUNHA; M H HIRATA; Chong Ae KIM; S T SANTOS; R D C HIRATA

1999 Trabalho em evento
LS Genetics

Cromossomo 4 em anel: estrutura e correlação genótipo-fenótipo

45º Congresso Nacional de Genética

C I E CASTRO; D R BERTOLA; S M M SUGAYAMA; Chong Ae KIM; C P KOIFFMANN

ISBN 14154757
1999 Trabalho em evento
LS Genetics

Dissomia uniparenteral como causa de doença genética

45º Congresso Nacional de Genética

S A S FONSECA; C L BOROVICK; R MULLER; Chong Ae KIM; A M MORGANTE

ISBN 14154757
1999 Trabalho em evento
HS Genetics (clinical)

Estudo genético-clínico e molecular da neurofibromatose

45º Congresso Nacional de Genética

L A PRAXEDES; R C Migroni NETO; P A OTTO; Chong Ae KIM; F ARITA

ISBN 14154757
1999 Trabalho em evento
LS Genetics

Análise molecular de deleções 4p associadas com a síndrome de Wolf-Hirschhorn

45º Congresso Nacional de Genética

E P P SILVA; Chong Ae KIM; S M M SUGAYAMA; C Y UTAGAWA; C P KOIFFMANN

ISBN 14154757
1999 Trabalho em evento
HS Genetics (clinical)

Estudo dos sinais clínicos e relevância no diagnóstico da neurofibromatose

45º Congresso Nacional de Genética

L A PRAXEDES; R C Migroni NETO; P A OTTO; Chong Ae KIM; F ARITA

ISBN 14154757
1999 Trabalho em evento
LS Genetics

Síndrome de Pallister-Killian: detecção do i (12p) por Fish em mucosa oral

45º Congresso Nacional de Genética

C L BOROVICK; E Auler BITENCOURT; A P M SILVA; Chong Ae KIM; S M M SUGAYAMA et al

ISBN 14154757
1999 Trabalho em evento
HS Genetics (clinical)

Triagem de mutações no gene CFTR em 160 pacientes com fibrose cística do pâncreas

45º Congresso Nacional de Genética

A BERNADINO; A FERRI; M R Passos BUENO; Chong Ae KIM; C M A NAKAIE et al

ISBN 14154757
1999 Trabalho em evento
LS Genetics

Estudo da mutação R 334W em sete pacientes com fibrose cística do pâncreas

45º Congresso Nacional de Genética

K E MIRANDA; A L BERNARDINO; A FERRI; M R Passo BUENO; C M A NAKAIE et al

ISBN 14154757
1999 Trabalho em evento
LS Genetics

The gene for the camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) encodes a secreted proteoglycan that in essential to normal joint function

Annual Meeting. The American Society of Human Genetics

J MARCELINO; J D CARPTEM; W M SUWAIRI; S SCHWARTZ; C ROBBINS et al

1999 Trabalho em evento
HS Genetics (clinical)

Noonan syndrome: a clinical and genetic study of 31 patients

Annual Meeting. The American Society of Human Genetics

D R BEROLA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; L M J ALBANO; J D A CARNEIRO et al

1999 Trabalho em evento
LS Genetics

Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations

Annual Meeting. The American Society of Human Genetics

A L BERNARDINO; A FERRI; M R Passo BUENO; Chong Ae KIM; C M A NAKAIE et al

1999 Trabalho em evento
HS Genetics (clinical)

Clinical study and use of FISH analysis to diagnostic approach of Brazilian patients with Williams-Beuren syndrome

Annual Meeting of the American Society of Human Genetics

Sofia Mizuko Miura SUGAYAMA; M L F CHAUFFAILLE; C J ABE; D R BEROLA; L ALBANO et al

1999 Trabalho em evento
HS Embryology

Dysostosis spondylocosital: a clinical study of 14 patients

Annual Meeting. The American Society of Human Genetics

S M M UTAGAWA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; Debora Romeo BERTOLA; L A N OLIVEIRA et al

1999 Trabalho em evento
HS Genetics (clinical)

Dilemma to chronic ventilation in Werdnig-Hoffmann disease: study of 15 patients

Annual Meeting. The American Society of Human Genetics

Chong Ae KIM; P LECUSSAN; E B CASELLA; M J ALBANO; G OSELKA

1999 Trabalho em evento
HS Genetics (clinical)

Estudo clínico-laboratorial de Mucopolissacaridoses: experiência de cinco anos

XI Congresso Brasileiro de Genética Clínica

L M J ALBANO; Sofia Mizuko Miura SUGAYAMA; Debora Romeo BERTOLA; Fávia PUPPI; C Y UTAGAWA et al

1999 Trabalho em evento
LS Genetics

The gene for the camptodactily-arthropathy-coxa vara-pericarditis syndrome (CACP) encode a secreted proteoglycan that is essential to normal joint function

49th Annual Meeting. The American Society of Human Genetics

J MARCELINO; J D CARPTEM; W M SUWAIRI; S SCHWARTZ; C ROBBINS et al

1999 Trabalho em evento
HS Genetics (clinical)

Noonan syndrome: a clinical and genetic study of 31 patients

49th Annual Meeting. The American Society of Human Genetics

Debora Romeo BERTOLA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; L M J ALBANO; J D A CARNEIRO et al

1999 Trabalho em evento
HS Medicine (miscellaneous)

Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations

49th Annual Meeting. The American Society of Human Genetics

A L F BENARDINO; A FERRI; M R Passos BUENO; Chong Ae KIM; C M A NAKAIE et al

1999 Trabalho em evento
LS Genetics

Clinical study and use of FISH analysis to diagnostic approach of brazilian patients with Williams-beuren syndrome

49th Annual Meeting. The American Society of Human Genetics

Sofia Mizuko Miura SUGAYAMA; M L F CHAUFFAILLE; K T ABE; Debora Romeo BERTOLA; L M J ALBANO et al

1999 Trabalho em evento
HS Medicine (miscellaneous)

Dysostosis spondylocostal: a clinical study of 14 patients

49th Annual Meeting. The American Society of Human Genetics

C Y UTAGAWA; Chong Ae KIM; Sofia Mizuko Miura SUGAYAMA; D R BERTOLA; L A N OLIVEIRA et al

1999 Trabalho em evento
LS Genetics

A clinical; cytogenetic and molecular study of three Brazilian patients with supernumerary Inv Dup(15) marker chromosomes.

49th Annual Meeting. The American Society of Human Genetics

M C VARELA; C FRIDMAN; T E MATSUMOTO; Chong Ae KIM; F KOK et al

1999 Trabalho em evento
HS Medicine (miscellaneous)

Dilemma to chronic ventilation in Werdnig-Hoffmann disease: study of 16 patients

49th Annual Meeting. The American Society of Human Genetics

Chong Ae KIM; P LECUSSAN; E B CASELLA; L M J ALBANO; G OSELKA

1999 Trabalho em evento
HS Neurology (clinical)

Importance of cyanide-nitroprussiade test for the dianosis of homocystinuria

XX World Congress of Pathology/Laboratory Medicine; XXXIII Brazilian; IV Mercosul and the III Brazilian Congress of Laboratory Management

Sofia Mizuko Miura SUGAYAMA; Chong Ae KIM; M M S K INOUE; C Y UTAGAWA; D R BERTOLA et al

1999 Trabalho em evento
LS Neurology

Use of FISH analysis to diagnostic approach of 11 Brazilian patients with Williams-Beuren syndrome

XX World Congress of Pathology/Laboratory Medicine; XXXIII Brazilian; IV Mercosul and the III Brazilian Congress of Laboratory Management

S M M SUGAYAMA; Chong Ae KIM; K T ABE; L M J ALBANO; D R BERTOLA et al