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S M M Sugayama

Observed names: S M Sugayama, S. M. M. Sugayama, S.M.M. Sugayama, SMM Sugayama
OpenAlex ID: A5111967865
Prenatal exposure to misoprostol and vascular disruption defects: A case-control study
2000 · F.R. Vargas, L. Schuler-Faccini, et al. · American Journal of Medical Genetics · 135
AEC Syndrome and CHAND Syndrome: Further Evidence of Clinical Overlapping in the Ectodermal Dysplasias
2000 · D. R. Bertola, C. A. Kim, et al. · Pediatric Dermatology · 26
Evaluation of the immune humoral response of Brazilian patients with Rubinstein-Taybi syndrome
2010 · L.C. Torres, S.M.M. Sugayama, et al. · Brazilian Journal of Medical and Biological Research · 12
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Orientacao familiar preventiva: aspectos geneticos das doencas cardiovasculares e perspectivas futuras
1996 · Motomu Shimoda, S M M Sugayama, et al. · 7
New CBP mutations in Brazilian patients with Rubinstein–Taybi syndrome
2012 · KT Suzuki, LC Torres, et al. · Clinical Genetics · 4
Mutations of the homeobox gene ALX4 in parietal foramina and cranium bifidum: a component of DEFECT 11 syndrome.
2000 · Lampros A. Mavrogiannis, A Baxová, et al. · The American Journal of Human Genetics · 2
Rubinstein-Taybi syndrome: a human model for studying the role of CREBBP and EP300 genes in B cell regulation
2007 · Leuridan Cavalcante Torres, S M M Sugayama, et al. · UNIFESP Institutional Repository (Universidade Federal de São Paulo)
High levels of total and specific IgM antibodies in patients with Rubinstein-Taybi syndrome (RTS)
2006 · Magda M. Carneiro-Samapio, Luisa Torres, et al. · Abstracts
Evaluation of immunocompetence in patients with Rubinstein-Taybi Syndrome (RTS)
2006 · Luisa Torres, Magda Carneiro‐Sampaio, et al. · Abstracts
Importance of cyanide-nitroprusside test for the diagnosis of homocystinuria
1999 · S M M Sugayama, C. A. Kim, et al.
Estudo genetico-clinico de delecao intersticial do braco longo do cromossomo 13
1996 · Cristina Izquierdo Castro, S M M Sugayama, et al.
Sindrome do triplo x: relato de 3 casos
1996 · C Andrade, S M M Sugayama, et al.
Sindrome de robinow
1994 · C A Kim, S M M Sugayama, et al.
Interstitial deletion of the long arm of chromosome 14 involving band 14q31 in a boy with a mca / mr syndrome
1994 · Claudette Hajaj Gonzalez, S M M Sugayama, et al. · Resumenes
Sindrome de jarcho lecin: relato de 2 irmaos afetados e revisao de literatura
1994 · S M M Sugayama, E M Ribeiro, et al. · Genetics and Molecular Biology
Neurofibromatose tipo i , anemia falciforme e talassemia em um menino de 12 anos
1994 · Enilze Maria de Souza Fonseca Ribeiro, Cláudia Yamada Utagawa, et al. · Genetics and Molecular Biology
Sindrome de picnodisostose: relato de 3 casos
1994 · C Y Utagawa, E M Ribeiro, et al. · Genetics and Molecular Biology
Anomalia de pelger-huet: relato de tres casos e revisao da literatura
1994 · C Y Utagawa, M F Monaco, et al. · Resumos
Delecao do 18p e isocromossomo 18q em mosaico em um paciente com ptose palpebral , baixa estatura e retardo mental
1993 · S M M Sugayama, Anne C. Barbosa, et al. · Genetics and Molecular Biology
Micronucleos (mn) em frentistas de postos automotivos, antes e apos a utilizacao do metanol como combustivel
1992 · C A Kim, S M M Sugayama, et al. · Genetics and Molecular Biology
Sindrome de down: complicacoes neonatais
1992 · C A Kim, E M A Diniz, et al. · Revista Paulista de Pediatria
Anemia de fanconi: estudo clinico e citogenetico em duas irmas afetadas e sua familia
1991 · S M Sugayama, C A Kim, et al. · Programa
Works count: 22
Citation count: 186
H-index: 4
I10-index: 3
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