Departamento de Genética Médica

Resumos publicados em revistas de circulação internacional especializadas

  1. E.A.Parizotto, A.F.Ribeiro e C.S.Bertuzzo, ``Molecular characterisation of cystic fibrosis patients in the state of São Paulo (Brazil)'', Journal of Medical Genetics, 34(10), 877, (1997).
  2. G.Guerra Jr, A.T.M.Guerra, A.P.M.Faria, M.T.M.Baptista, R.B.P.Silva, M.Ceschini e I.A.Cardinalli, ``Chromosome constitution among true hermaphrodites Brazil : a different profile'', Frontiers in Endocrinology, 20, 240, (1997).
  3. D.B.Marmo, G.Guerra Junior, A.T.M.Guerra, M.T.M.Baptista, A.M.Morcillo, C.C.M.Medeiros, A.de A.Barros Filho e S.H.V.Marini, ``Turner Syndrome and Hashimoto Thyroiditis Association: The prevalence in 75 cases'', Pediatric Research, 41(2), 305, (1997).
  4. K.Metze, C.Hackel, V.C.Colussi, D.F.Cabral, O.Rettori, P.Iazetti, E.M.D.Nicola e J.H.Nicola, ``Photodynamic therapy in hyperbaric hyperoxia'', Pathology, Research and Practice, 193(5-6), 308, (1997).
  5. H.A.G.Teve, W.O.Arruda, P.C.B.Trevisol, I.Lopes Cendes, G.A.Rouleau e L.C.Werneck, ``Spinocerebellar ataxia: a genetic study in 30 Brazilian families'', Neurology, 48(suppl2), 177, (1997).
  6. C.Medeiros, G.Guerra Jr, S.Marini, D.Marmo, M.Baptista, A.P.M.Faria e A.T.M.Guerra, ``Turner syndrome and thyroid disease: a transversal study with paediatric patients in Brazil'', Pediatric Research, 48, 171, (1997).
  7. G.Guerra Jr, A.T.M.Guerra, M.Baptista, A.P.M.Faria, S.MArini e A.Morcillo, ``The evaluation of patients with sex ambiguity: a 6-year experience with 163 in Southeastern of Brazil'', Hormone Research, 48, 171, (1997).
  8. P.Silva, A.T.M.Guerra, G.Guerra, M.Baptista, M.Mello e S.Marini, ``Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Clinical expression and molecular characterization in 32 Brazilian patients'', Hormone Research, 48, 101, (1997).
  9. M.Baptista, S.Marini, P.Silva, A.Maorcillo, C.Medeiros, A.T.M.Guerra, D.Marmo e G.Guerra Jr, ``A preliminary study of final height in Brazilian girls with Turner syndrome'', Pediatric Research, 48, 60, (1997).
  10. M.T.M.Baptista, S.H.V.Marini, A.M.Morcillo, C.C.M.Medeiros, A.T.M.Guerra, D.B.Marmo e G.Guerra Junior, ``A preliminary study of final height in Brazilian girls with Turner Syndrome'', Hormone Research, 48(2), 201, (1997).
  11. C.C.M.Medeiros, G.Guerra Junior, S.H.V.Marini, D.B.Marmo, M.T.M.Baptista, A.P.M.Faria e A.T.M.Guerra, ``Turner Syndrome and Thyroid Disease: A transversal study with paediatric patients in Brazil'', Hormone Research, 48(2), 201, (1997).
  12. M.T.M.Baptista, S.H.V.Marini, P.O.A.Silva, A.M.Morcillo, C.C.M.Medeiros, A.T.M.Guerra, D.B.Marmo e G.Guerra Junior, ``A preliminary study of final height in brazilian girls with Turner syndrome'', Hormone Research, 48(2), 60, (1997).
  13. M.T.M.Baptista, S.H.V.Marini, A.M.Morcillo, C.C.M.Medeiros, A.T.M.Guerra, D.B.Marmo e G.Guerra Junior, ``A preliminary study of final height in Brazilian girls with Turner Syndrome'', Hormone Research, 48(suppl2), 60, (1997).
  14. P.O.A.Silva, A.T.M.Guerra, G.Guerra Junior, M.T.M.Baptista, M.P.Mello e S.H.V.Marini, ``Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: clinical expression and molecular characterization in 32 brazilian patients'', Hormone Research, 48(2), 101, (1997).
  15. G.Guerra Junior, A.T.M.Guerra, M.T.M.Baptista, A.P.M.Faria, S.H.V.Marini e A.M.Morcillo, ``The evaluation of patients with sex ambibuity: a 6-year experience with 163 in southern of Brazil'', Hormone Research, 48(2), 117, (1997).
  16. C.C.M.Medeiros, G.Guerra Junior, S.H.V.Marini, D.B.Marmo, M.T.M.Baptista, A.P.M.Faria e A.T.M.Guerra, ``Turner syndrome and thyroid disease: a transversal study with paediatric patients in Brazil'', Hormone Research, 48(2), 171, (1997).
  17. A.T.M.Guerra, G.Guerra Jr, A.P.M.Faria, M.T.M.Baptista, Z.Z.L.Bittencourt, M.Ceschini e I.A.Cardinalli, ``The evaluation of patients with anomalies of sex differentiation: a 6-year experience with 281 patients in Brazil'', Frontiers in Endocrinology, 20, 243, (1997).
  18. L.Ferraz, G.Guerra Jr, M.Baptista, A.T.M.Guerra e C.Hackel, ``Mutacao Gly-196-Ser no gene da 5 alfa-redutase II em paciente com pseudo-hermafroditismo masculino'', Brazilian Journal of Genetics, 20(supl), 238, (1997).
  19. F.C.Reis, D.Y.J.Norato, C.Hackel, R.P.Oliveira Sobrinho, S.P.Davidsohn e E.L.Sartorato, ``Estudo molecular da glicogenose tipo Ia (Doença de Von Gierke)'', Brazilian Journal of Genetics, 20(3), 234, (1997).
  20. H.G.Serra, C.S.Bertuzzo, T.C.L.Silva, C.C.Rossi e I.A.Paschoal, ``High prevalence of alpha 1-antitrypsin S allele in a Brazilian Population'', Chest, 112(3), 825, (1997).
  21. I.Lopes Cendes, E.Andermann, A.Nechiporuk, E.Attig, S.Bosh, M.Wagner, F.Andermann, F.Gerstenbrand, M.I.Botez, H.Teive, S.Jain, S.M.Pulst e G.A.Rouleau, ``Frequency and molecular characteristics of the spinocerebellar ataxia type 2 mutation'', Neurology, 48(suppl2), 177, (1997).
  22. H.A.G.Teive, W.O.Arruda, P.C.Trevisol-Bittencourt, I.Lopes Cendes, I.Silveira e G.A.Rouleau, ``Ataxias espinocerebelares : avaliação preliminar de 20 famílias através de estudos com genética molecular'', Arquivos de Neuro-Psiquiatria, 54(supl), 252, (1997).
  23. S.Premkumar, I.Lopes Cendes, A.L.DeStefano, G.A.Rouleau e L.A.Farrer, ``Patterns of transmission and correlation between CAG repeat and onset age in an ethnically diverse population of spinocerebellar ataxia type 2 (SCA2)'', American Journal of Human Genetics, 61(supp), 318, (1997).
  24. S.Hayes, I.Lopes Cendes, E.Andermann, C.Gaspar e G.A.Rouleau, ``Investigation of spinocerebellar ataxia type 6 (SCA6) in a group os spinocerebellar ataxia patients: frequency, allele distribution and clinical features'', American Journal of Human Genetics, 61(supp), 310, (1997).
  25. R.M.Volpe, M.T.Aquino e D.Y.J.Norato, ``An alternative way to construct and evaluate educacional software Journal of Medical Informatics Association'', Journal of Medical Informatics, 1, 1013, (1997).
  26. I.Lopes Cendes, E.Andermann, S.Hayes, E.Attig, S.Bosch, M.Wagner, F.Andermann, F.Gerstenbrand, M.I.Botez, H.Teive, F.Cardoso, S.Jain, Y.Robitaille, S.Pulst, S.Kish e G.A.Rouleau, ``Clinical, genetic and molecular studies in spinocerebellar ataxia type 2'', Journal of the Neurological Sciences, s, 41, Serie: 150 suppl., (1997).
  27. P.Maciel, C.Gaspar, L.Guimaraes, A.Dias, K.Arvidsson, S.Hayes, I.Lopes Cendes, J.Goto, A.Sousa, J.Sequeiros e G.A.Rouleau, ``Effect of the normal chromosome on the instability of the expanded CAG repeat in the MJD1 gene'', Journal of the Neurological Sciences, s, 314, Serie: 150 suppl., (1997).
  28. P.Coutinho, J.Guimaraes, J.Barros, J.L.Loureiro, P.Ribeiro, R.Chorao, E.Lourenço, C.Alves, J.V.Santos, I.Silveira, P.Maciel, C.Gaspar, I.Lopes Cendes, G.Rouleau e J.Sequeiros, ``Autossomal dominant ataxias in Portugal: review of 106 families'', Journal of the Neurological Sciences, 150(suppl), 40, Serie: s40, (1997).
  29. R.Joober, C.Benkelfat, J.L.Mandel, I.Lopes Cendes, S.Lal, P.Lalonde, A.Labelle, R.Palmour, G.O'Driscoll e G.A.Rouleau, ``Polyglutamine containing proteins in schizophrenia'', Journal of Medical and Biological Research(42), 98, Serie: 98S, (1997).
  30. N.J.P.Pavani, A.F.A.Braga, R.P.de Souza e L.A.Magna, ``Bloqueadores de Canais de Calcio e Sevoflurano. Estudo Experimental em Caes'', Revista Brasileira de Anestesiologia, 47(-), 8, Serie: (Suplemento 22), (1997).
  31. N.J.P.Pavani, A.F.A.Braga, J.M.D.Oliveira e L.A.Magna, ``Interacao entre Metoprolol, Bloqueadores do Canal de Calcio e Sevoflurano. Estudo Experimental em Caes'', Revista Brasileira de Anestesiologia, 47(-), 9, Serie: (Suplemento 22), (1997).
  32. N.J.P.Pavani, F.S.Soeiro, E.C.B.Aleixo e L.A.Magna, ``Interacao entre Metoprolol e Sevoflurano. Estudo Experimental em Caes'', Revista Brasileira de Anestesiologia, 47, 9, Serie: Suplemento 22 - Temas Livres do 44o. CBA, (1997).
  33. C.Gaspar, J.Goto, I.Lopes Cendes, S.Hayes, K.Arvidsson, P.Maciel, I.Silveira, P.Coutinho, G.Stevanin, A.DeStefano, O.Riess, H.Sasaki, P.Giunti, N.Wood, E.Brunt, L.Tranebjaerg, G.Nicholson, J.J.Higgins, M.Lauritzen, W.Watanabe, V.Volpini, M.Hsieh, B.Soong ``Founder effect study in a large group of Machado-Joseph disease families with different ethnic origins'', Journal of the Neurological Sciences, 150(supplS), 41, Serie: s41, (1997).

Fri Nov 13 10:37:14 BDB 1998