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Material Type: Artigo
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Cor pulmonale in Manson's schistosomiasis. I. Frequency in necropsy material; pulmonary vascular changes caused by schistosome ovaLOPES DE FARIA, JThe American journal of pathology, 1954-01, Vol.30 (1), p.167-193 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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Expression of developmentally defined retinal phenotypes in the histogenesis of retinoblastomaGonzalez-Fernandez, F ; Lopes, MB ; Garcia-Fernandez, JM ; Foster, RG ; De Grip, WJ ; Rosemberg, S ; Newman, SA ; VandenBerg, SRThe American journal of pathology, 1992-08, Vol.141 (2), p.363-375 [Periódico revisado por pares]BALTIMORE: ASIPTexto completo disponível |
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Material Type: Artigo
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Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate regionLOPES-CENDES, I ; ANDERMANN, E ; ATTIG, E ; CENDES, F ; BOSCH, S ; WAGNER, M ; GERSTENBRAND, F ; ANDERMANN, F ; ROULEAU, G. AAmerican journal of human genetics, 1994-05, Vol.54 (5), p.774-781 [Periódico revisado por pares]Chicago, IL: University of Chicago PressTexto completo disponível |
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Material Type: Artigo
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A retrospective study of the use of bovine pericardium, dura mater, and polypropylene mesh as reinforcement materials in abdominal and thoracic wall reconstructionMarques, Américo ; Lopes, Ademar ; Yojo, Lúcia M. ; Brenda, Elizabeth ; Amarante, Marco Túlio J. ; Pereira, Max D. ; Torloni, HumbertoCurrent therapeutic research, 1995-05, Vol.56 (5), p.492-497 [Periódico revisado por pares]Belle Mead, NJ: EM Inc USATexto completo disponível |
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Material Type: Artigo
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Correlation between CAG repeat length and clinical features in Machado-Joseph diseaseMACIEL, P ; GASPAR, C ; NEZARATI, M. M ; CORWIN, L. I ; LOPES-CENDES, I ; ROOKE, K ; ROSENBERG, R ; MACLEOD, P ; FARRER, L. A ; SEQUEIROS, J ; ROULEAU, G. A ; DESTEFANO, A. L ; SILVEIRA, I ; COUTINHO, P ; RADVANY, J ; DAWSON, D. M ; SUDARSKY, L ; GUIMARAES, J ; LOUREIRO, J. E. LAmerican journal of human genetics, 1995-07, Vol.57 (1), p.54-61 [Periódico revisado por pares]Chicago, IL: University of Chicago PressTexto completo disponível |
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Material Type: Artigo
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Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences : New tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1ALOPES, J ; LEGUERN, E ; GOUIDER, R ; TARDIEU, S ; ABBAS, N ; BIROUK, N ; GUGENHEIM, M ; BOUCHE, P ; AGID, Y ; BRICE, AAmerican journal of human genetics, 1996, Vol.58 (6), p.1223-1230 [Periódico revisado por pares]Chicago, IL: University of Chicago PressTexto completo disponível |
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Material Type: Artigo
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The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15qCASAUBON, L. K ; MELANSON, M ; ROULEAU, G. A ; LOPES-CENDES, I ; MARINEAU, C ; ANDERMANN, E ; ANDERMANN, F ; WEISSENBACH, J ; PREVOST, C ; BOUCHARD, J.-P ; MATHIEU, JAmerican journal of human genetics, 1996, Vol.58 (1), p.28-34 [Periódico revisado por pares]Chicago, IL: University of Chicago PressTexto completo disponível |
8 |
Material Type: Artigo
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Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research GroupLopes, J ; LeGuern, E ; Gouider, R ; Tardieu, S ; Abbas, N ; Birouk, N ; Gugenheim, M ; Bouche, P ; Agid, Y ; Brice, AAmerican journal of human genetics, 1996-06, Vol.58 (6), p.1223-1230 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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Diagnósticos de enfermagem de pacientes em unidades de terapia intensivaPasini, Dolores ; Alvim, Iracema ; Kanda, Luiza ; Mendes, Rita do Socorro Pereira ; Cruz, Diná de Almeida Lopes Monteiro daRevista da Escola de Enfermagem da U S P, 1996-12, Vol.30 (3), p.501-518 [Periódico revisado por pares]Universidade de São Paulo, Escola de EnfermagemTexto completo disponível |
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Material Type: Artigo
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Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24Phillips, H.A. ; Scheffer, I.E. ; Crossland, K.M. ; Bhatia, K.P. ; Fish, D.R. ; Marsden, C.D. ; Howell, S.J.L. ; Stephenson, J.B.P. ; Tolmie, J. ; Plazzi, G. ; Eeg-Olofsson, O. ; Singh, R. ; Lopes-Cendes, I. ; Andermann, E. ; Andermann, F. ; Berkovic, S.F. ; Mulley, J.C.American journal of human genetics, 1998-10, Vol.63 (4), p.1108-1116 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |