Departamento de Genética Médica

Resumos em Revistas de Circ. Internac. Espec.

  1. E. Kobayashi, S.C.de Sousa, T.C.L. Silva, Carlos A.M. Guerreiro, Iscia Lopes Cendes e Fernando Cendes, "Epilepsia de Lobo Temporal Familiar", Brazilian Journal of Epilepsy and Clínical Neurophysiology, 4 , 85, (1998). [72596]
  2. E. Kobayashi, T.C.L. Silva, S.C. Sousa, Carlos A.M. Guerreiro, A.E. Scotoni, Marilisa Mantovani Guerreiro, F. Cendes e Iscia Lopes Cendes, "Familial Idiopathic Epilepsies", Arquivos de Neuro-Psiquiatria, 56 (s1), 205, (1998). [74511]
  3. H. Teive, D. Sá, W. Arruda, P. Trevisol, L. Werneck, Iscia Lopes Cendes e G.A. Rouleau, "Is It Possible To Differentiate Machado-joseph Disease From Others spinocerebellar Ataxias Based On Clínical Grounds?", Arquivos de Neuro-Psiquiatria, 56 (s1), 209, (1998). [74513]
  4. M.F.A.G. Camargo, F.C. Costa, T.C.L. Silva e Iscia Lopes Cendes, "Clínical And Genetic Heterogeneity In spinocerebellar Ataxias", Arquivos de Neuro-Psiquiatria, 56 (s1), 250, (1998). [74515]
  5. Antonia Paula M Faria e Gisele S. Oliveira, "Clínical Features Of Kabuki Syndrome In Ten Brazilian Children", American Journal of Human Genetics, 63 (4), 623, (1998). [78019]
  6. Sofia Helena Valente Lemos-marini, Maria Tereza Matias Baptista, P.O.A. Silva, André Moreno Morcillo, Andrea Trevas M Guerra, Gil Guerra Junior, Sofia Helena Valente Lemos-marini, Maria Tereza Matias Baptista, André Moreno Morcillo, Andrea Trevas M Guerra, Denise Barbieri Marmo e Gil Gu, "Final Height In Girls With Turner Syndrome", Pediatric Research, 43 (2), 297, (1998). [80940]
  7. E.G. Stuchi-perez, Maria Tereza Matias Baptista, Gil Guerra Junior, M.R. Scolfaro, Andrea Trevas M Guerra, Antonia Paula M Faria, R.B.P. Silva, M. Ceschini, M. Castro, R. Rey e I Cardinalli, "Hormônio Anti-mülleriano: Aplicação Clínica em Intersexo", Arquivos Brasileiros de Endocrinologia e Metabologia, 42 (5), 278, (1998). [80945]
  8. Denise Pontes Cavalcanti, H. Serra, J.I.C.F. Neri, B.R. Alvares, G.A. Souza e I.A. Cardinalli, "Tibial Aplasia, Polidactyly, Triphalangeal Thumbs And Müllerian Duct Malformations: a New Syndrome?", American Journal of Human Genetics, 63 (Suppl, 99, (1998). [81345]
  9. Edi Lucia Sartorato, R.C.V. Carrara, W.O. Bragança, R. Yamasaki, Christine Hackel e J.M. Pina-neto, "Molecular Approach In The Study Of Idiopathic Infertile Male", American Journal of Human Genetics, 63(4 (Suppl, 384, (1998). [81424]
  10. E.M. Thomaz, A.M. Sakamoto, E.A. Donadi, Luis Alberto Magna e Maria Helena S. Kraemer, "Moleculat Analysis And Distribuition Of The Mhc Class II Alleles And Haplotipes In The Brazilian Population Of The City Of Campinas", Human Immunology, 59 (Suppl, 57, (1998). [81450]
  11. Edi Lucia Sartorato, F.C. Reis, Denise Yvonne J Norato e Christine Hackel, "A Novel Mutation In a Brazilian Patient With Glycogen Storage Disease Type 1a", Journal of Inherited Metabolic Disease, 21 , 447, (1998). [81451]
  12. M.D. Dágostino, E. Andermann, S.F. Berkovic, Iscia Lopes Cendes, Fernando Cendes, B. Abou-khalil, M. Javidan, M. Labuda, M. Pandolfo, T. Hudson e F. Andermann, "Familial Temporal Lobe Epilepsy (Ftle): Clínical Characterization And Preliminary Linkage Studies", American Journal of Human Genetics, 63 (Supp, 101, (1998). [81733]
  13. B.A. Minassian, J. Lee, J. Herbrick, J.. Huizenga, A. Mungall, I. Dunham, C.Y. Fong, Iscia Lopes Cendes, L.C. Tsui, A.V. Delgado-escueta, G.A. Rouleau e S.W. Scherer, "Molecular Genetics Of Lafora's Progressive Myoclonus Epilepsy", American Journal of Human Genetics, 63 (Sup A, 374, (1998). [81737]