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Departamento de Genética Médica
Produções / Artigos publicados em periódicos
Artigos publicados em periódicos especializados arbitrados de circulação (internacional)
1.
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de Souza, S.J. (autor); Camargo, AA (autor); Briones, MR (autor); Costa, FF (autor); Nagai, MA (autor); Verjovski-Almeida, S (autor); Zago, MA (autor); Andrade, LE (autor); Carrer, H (autor); El-Dorry, HF (autor); Espreafico, EM (autor); Habr-Gama, A (autor); Gianella-Neto, D (autor); Goldman, GH (autor); Gruber, A (autor); Hackel, Christine (autor); Kimura, ET (autor); Maciel, RM (autor); Marie, SK (autor); Martins, EA (autor); Nobrega, MP (autor); Paco-Larson, ML (autor); Pardini, MI (autor); Pereira, GG (autor); Pesquero, JB (autor); Rodrigues, V (autor); Rogato, SR (autor); da Silva, ID (autor); Sogayar, MC (autor); de Fatima Sonati, M (autor); "Identification of human chromosome 22 transcribed sequences with ORF expressed sequence tags.", 12/2000, Proc. Natl. Acad. Sci. USA., Vol. 97, Fac. 23, pp.12690-12693, SP, BRASIL, 2000
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2.
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Sartorato, Edi Lucia (autor); Gottardi, Elena (autor); Oliveira, Camila Andréa de (autor); Magna, Luis Alberto (autor); Annichino-Bizzacchi, Joyce Maria (autor); Seixas, Carlos Augusto (autor); Guerra, Andrea Trevas M (autor); "Determination of the frequency of the 35delG allele in Brazilian neonates.", 11/2000, Clinical Genetics, Vol. 58, pp.339-340, Copenhagen, DINAMARCA, 2000 *
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3.
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Cardoso, Francisco (autor); Oliveira, José Teotonio (autor); Solher-Puccioni, Marzia (autor); Fernandes, Alexandre R. (autor); Mattos, James Pitágoras de (autor); Lopes Cendes, Iscia (autor); "Eyelid Dystonia in Machado-Joseph Disease.", 11/2000, Movement disorders, Vol. 15, Fac. 5, pp.1028-1030, New York, ESTADOS UNIDOS, 2000
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4.
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Filardi, S. (autor); Marques-Neto, J.F. (autor); Guerreiro, C.A.M. (autor); Magna, Luis Alberto (autor); "Patients undergoing anticonvulsivant therapy at low risk for bone disease have normal bone mineral density, normal serum levels of vitamin D and slight decrease in the calcium serum level.", 10/2000, Journal of Clinical Rheumatology, Vol. 6, Fac. 3, pp.164-165, Baltimore, ESTADOS UNIDOS, 2000
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5.
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Kobayashi, Eliane (autor); Cendes, Fernando (autor); Sousa, Solange C. (autor); Scotoni, Anna E. (autor); Carvalho, Maria Imaculada (autor); Guerreiro, Marilisa Mantovani (autor); Guerreiro, Carlos A.M. (autor); Lopes Cendes, Iscia (autor); "Epilepsias parciais familiares.", 09/2000, Arquivos de Neuro-Psiquiatria, Vol. 58, Fac. 3B, pp.862-868, Sao Paulo, SP, BRASIL, 2000 *
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6.
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Filardi, S. (autor); Guerreiro, Carlos A.M. (autor); Magna, Luis Alberto (autor); Marques Neto, João Francisco (autor); "Bone mineral density, vitamin D and anticonvulsant therapy.", 09/2000, Arquivos de Neuro-Psiquiatria, Vol. 58, Fac. 3A, pp.616-620, Sao Paulo, SP, BRASIL, 2000 *
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7.
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Gonçalves, N.S. (autor); Pinho, J.R. (autor); Moreira, R.C. (autor); Saraceni, C.P. (autor); Spina, A.M. (autor); Stucchi, R.B. (autor); Filho, A.D. (autor); Magna, Luis Alberto (autor); Gonçalves Jr., F.L. (autor); "Hepatitis E vírus immunoglobulin G antibodies in different populations in Campinas, Brazil.", 09/2000, Clinical and Diagnostic Laboratory Immunology, Vol. 7, Fac. 5, pp.813-816, Washington, ESTADOS UNIDOS, 2000
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8.
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Billis, Athanase (autor); Magna, Luis Alberto (autor); "Prostate elastosis: a microscopic feature useful for the diagnosis of postatrophic hyperplasia.", 09/2000, Archives of Pathology and Laboratory Medicine, Vol. 124, Fac. 9, pp.1306-1309, Waukegan, ESTADOS UNIDOS, 2000 *
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9.
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Marques-de-Faria, Antonia Paula (autor); "A boy with mental retardation, blepharophimosis and hypothyroidism: a diagnostic dilemma between Young-Simpson and Ohdo syndrome.", 07/2000, Clinical Dysmorphology, Vol. 9, pp.199-204, Londres, REINO UNIDO, 2000
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10.
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Compri, Mariane Bernadete (autor); Saad, Sara T. Olalla (autor); Ramalho, Antonio Sergio (autor); "Investigação genético-epidemiológica e molecular da deficiência de G-6-PD em uma comunidade brasileira.", 07/2000, Cadernos de Saude Publica, Vol. 16, Fac. 2, pp.335-342, Rio de Janeiro, RJ, BRASIL, 2000
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11.
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Stuchi-Peres, Eliana Gabas (autor); Baptista, Maria Tereza Matias (autor); Lukas-Croisier, C. (autor); Scolfaro, M.R. (autor); Hackel, Christine (autor); Guerra, Andrea Trevas M (autor); Castro, M. (autor); Guerra Junior, Gil (autor); Marques-de-Faria, Antonia Paula (autor); "Evaluation of the tubular and interstitial function of the testis in 46, XY patients with ambiguous genitalia.", 06/2000, Journal of Pediatric Endocrinology and Metabolism, Vol. 13, pp.605-612, Londres, REINO UNIDO, 2000 *
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12.
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Lopes Cendes, Iscia (autor); Scheffer, I.E. (autor); Berkovic, S.F. (autor); Rousseau, M. (autor); Andermann, E. (autor); Rouleau, G.A. (autor); "A new Locus for generalized epilepsy with febrile seizures plus maps to chromosome 2.", 06/2000, American Journal of Human Genetics, Vol. 66, pp.698-701, Chicago, ESTADOS UNIDOS, 2000
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13.
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Gonçalves, F.L. Jr (autor); Stucchi, R.S. (autor); Pavan, M.H. (autor); Escanhoela, C.A. (autor); Yamanaka, A. (autor); Magna, Luis Alberto (autor); "A clinical, epidemological, laboratorial, histological and ultrasonographical evaluation of anti-HCV EIA-2 positive blood donors.", 06/2000, Revista Instituto de Medicina Tropical de São Paulo, Vol. 42, Fac. 3, pp.147-152, São Paulo, SP, BRASIL, 2000
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14.
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Lima e Silva, Tereza Cristina (autor); Serra, Heliane Guerra (autor); Bertuzzo, Carmem Silvia (autor); Lopes Cendes, Iscia (autor); "Molecular diagnosis of Huntington Disease in brazilian patients.", 05/2000, Arquivos de Neuro-Psiquiatria, Vol. 58, Fac. 1, pp.11-17, Sao Paulo, SP, BRASIL, 2000
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15.
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Steiner, Carlos Eduardo (autor); Guerreiro, Marilisa Mantovani (autor); Marques-de-Faria, Antonia Paula (autor); "Differential Diagnosis of Autism: The Importance of Medical Evaluation to Genetic Counseling.", 05/2000, NADD Bulletin, Vol. 3, Fac. 3, pp.48-53, Kingston, ESTADOS UNIDOS, 2000 *
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16.
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Hayes, Sean (autor); Turecki, Gustavo (autor); Brisebois, Kateri (autor); Lopes Cendes, Iscia (autor); Gaspar, Claudia (autor); Riess, Olaf (autor); Ranum, Laura P.W. (autor); Pulst, Stefan-M. (autor); Rouleau, Guy A. (autor); "CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)", 05/2000, Human Molecular Genetics, Vol. 9, Fac. 12, pp.1753-1758, REINO UNIDO, 2000
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17.
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Steiner, Carlos Eduardo (autor); Marques-de-Faria, Antonia Paula (autor); "Growth deficiency, mental retardation and unusual facies.", 04/2000, Clinical Dysmorphology, Vol. 9, Fac. 2, pp.155-157, Londres, REINO UNIDO, 2000
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18.
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Steiner, Carlos Eduardo (autor); Torriani, Martin P. (autor); Norato, Denise Yvonne J (autor); Marques-de-Faria, Antonia Paula (autor); "Spondylocarpotarsal Synostosis With Ocular Findings.", 03/2000, American Journal of Medical Genetics, Vol. 91, Fac. 2, pp.131-134, New York, NY, ESTADOS UNIDOS, 2000 *
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19.
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Ramalho, Antonio Sergio (autor); Paiva e Silva, Roberto Benedito (autor); "Community Genetics: a new discipline and its application in Brazil.", 03/2000, Cadernos de Saude Publica, Vol. 16, Fac. 1, pp.261-263, Rio de Janeiro, RJ, BRASIL, 2000
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20.
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Potério, MB (AUTOR); Cardillo, JA (AUTOR); Senne, FMB (AUTOR); Pelegrino, R (AUTOR); Kara José, Newton (AUTOR); Norato, Denise Yvonne J (AUTOR); Potério, GMB (AUTOR); "The Feasibility of Introducing a Visual Screening Test for Children during Vaccnination Campaigns.", 03/2000, Journal of Pediatric Ophthalmology and Strabismus, Vol. 37, Fac. 2, pp.68-72, Thorofare, New Jersey, ESTADOS UNIDOS, 2000 *
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21.
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Lima e Silva, Tereza Cristina (autor); Serra, Heliane Guerra (autor); Bertuzzo, Carmem Silvia (autor); Lopes Cendes, Iscia (autor); "Molecular diagnosis of Huntington disease in Brazilian patients.", 02/2000, Arquivos de Neuro-Psiquiatria, Vol. 58, Fac. 1, pp.11-17, Sao Paulo, SP, BRASIL, 2000
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22.
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Assumpção, Juliana Godoy (autor); Hackel, Christine (autor); Marques-de-Faria, Antonia Paula (autor); Mello, Maricilda Palandi (autor); "Molecular mapping of an idic (y6) chromosome in a Ulrich-Turner patient.", 01/2000, American Journal of Medical Genetics, Vol. 91, Fac. 2, pp.85-88, New York, NY, ESTADOS UNIDOS, 2000 *
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23.
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Marques-de-Faria, Antonia Paula (autor); Guerra, Andrea Trevas M (autor); Guerra Junior, Gil (autor); Baptista, Maria Tereza Matias (autor); "A boy wih mental retardation, blepharophimosis and hypothyroidism: a diagnostic dilema between Young-Simpson and Ohdo syndrome", 01/2000, Clinical Dysmorphology, Vol. 9, Fac. 1, pp.1-6, Londres, REINO UNIDO, 2000 *
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* Esta produção está associada também a outros órgãos
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