Distrofia muscular congênita de Ullrich moderadamente progressiva von Carakushansky, Gerson, Ribeiro, Marcia Gonçalves, Kahn, Evelyn

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Moderately progressive Ullrich congenital muscular dystrophy von Carakushansky, Gerson, Ribeiro, Marcia Gonçalves, Kahn, Evelyn

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Mutation Analysis of Patients with Hermansky-Pudlak Syndrome: A Frameshift Hot Spot in the HPS Gene and Apparent Locus Heterogeneity von Oh, Jangsuk, Ho, Lingling, Ala-Mello, Sirpa, Amato, Dominick, Armstrong, Linda, Bellucci, Sylvia, Carakushansky, Gerson, Ellis, Julia P., Fong, Chin-To, Green, Jane S., Heon, Elise, Legius, Eric, Levin, Alex V., Nieuwenhuis, H. Karel, Pinckers, A., Tamura, Naoaki, Whiteford, Margo L., Yamasaki, Hisato, Spritz, Richard A.

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Ligneous Periodontitis and Ehlers‐Danlos Syndrome von Pierro, Viviane S.S., Vazquez‐Sullca, Ramon, Vieira, Áurea Simone Barrôso, Takiya, Christina Maeda, Carakushansky, Gerson, Feres‐Filho, Eduardo J.

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Forma recessiva da síndrome de Freeman-Sheldon: relato de dois irmãos afetados von Carakushansky, Gerson, Paiva, Isaías S., Evelyn, Kahn, Ribeiro, Márcia G.

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Forma recessiva da síndrome de Freeman-Sheldon: relato de dois irmãos afetados Recessive type of Freeman-Sheldon syndrome: report of two affected siblings von Gerson Carakushansky, Isaías S. Paiva, Kahn Evelyn, Márcia G. Ribeiro

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Recessive type of Freeman-Sheldon syndrome - report of two affected siblings von Carakushansky, G, Paiva, I S, Kahn, E, Ribeiro, M G

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Diploid/triploid mosaicism: Further delineation of the phenotype von Carakushansky, Gerson, Teich, Evelyn, Ribeiro, Marcia G., Horowitz, Dafne D. G., Pellegrini, Sandra

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Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients von Lopes-Cendes, I, Teive, H G, Calcagnotto, M E, Da Costa, J C, Cardoso, F, Viana, E, Maciel, J A, Radvany, J, Arruda, W O, Trevisol-Bittencourt, P C, Rosa Neto, P, Silveira, I, Steiner, C E, Pinto Júnior, W, Santos, A S, Correa Neto, Y, Werneck, L C, Araújo, A Q, Carakushansky, G, Mello, L R, Jardim, L B, Rouleau, G A

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Forma recessiva da síndrome de Freeman-Sheldon: relato de dois irmãos afetados von Carakushansky, Gerson, Paiva, Isaías S., Evelyn, Kahn, Ribeiro, Márcia G.

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Síndrome oral-facial-digital: relato de um caso com anomalias do sistema nervoso central von Carakushansky, Gerson, Machado, Aluizio H. de Andrade

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Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients Freqüência das mutações que causam ataxi... von Iscia Lopes-Cendesi, Hélio G.A. Teive, Maria E Calcagnotto, Jaderson C. da Costa, Francisco Cardoso, Erika Viana, Jaime A. Maciel, João Radvany, Walter O. Arruda, Paulo C. Trevisol-Bittencourt, Pedro Rosa Neto, Isabel Silveira, Carlos E. Steiner, Walter Pinto-Júnior, André S. Santos, Ylmar Correa Neto, Lineu C. Werneck, Abelardo Q.C. Araújo, Gerson Carakushansky, Luiz R. Mello, Laura B. Jardim, Guy A. Rouleau

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Achondroplasia associated with Down syndrome von Carakushansky, Gerson, Carakushansky, Gerson, Rosembaum, Stella, Ribeiro, Marcia G., Kahn, Evelyn, Carakushansky, Mauri

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Síndrome oral-facial-digital: relato de um caso com anomalias do sistema nervoso central Oral-facial-digital syndrome: report of a case with abnormalities of the central nervous sy... von Gerson Carakushansky, Aluizio H. de Andrade Machado

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Síndrome oral-facial-digital: relato de um caso com anomalias do sistema nervoso central von Carakushansky, Gerson, Machado, Aluizio H. de Andrade

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LYSERGIDE AND CANNABIS AS POSSIBLE TERATOGENS IN MAN von Carakushansky, Gerson, Neu, RichardL, Gardner, LyttI

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Identical twin discordance for the Brachmann-de Lange syndrome revisited von Carakushansky, Gerson, Aguiar, Marcos B., Gonçalves, Marcia R., Berthier, Clélia O., Kahn, Evelyn, Carakushansky, Mauri, Pena, Sergio D. J.

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Transplacental Passage and Persistence in Serum for 6 9/12 Years of Iophenoxic Acid (Teridax) in a Child von Carakushansky, Gerson, Cárdenas, Luis E., Gardner, Lytt I.

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XYY WITH ABNORMAL GENITALIA von Carakushansky, Gerson, Neu, RichardL, Gardner, LyttI

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Intercorrências clínicas na Síndrome de Turner von Guimarães, Marília M., Guerra, Carla T.G., Alves, Solange T.F., Cunha, Maria C.S.A., Marins, Luiz A., Barreto, Luiz F.M., Teich, Evelyn, Santos, Flávia N., Ornellas, José F.R., Carakushansky, Gerson, Pinheiro, Gustavo, Oliveira, Helena P., Beserra, Isabel C.R., Ghiaroni, Juraci, Peixoto, Marcelo V., Farias, Maria L.F., Lanfredi, Mônica M.A., Proença, Munira A., Ramalho, Paula P., Pinheiro, Pedro S., Zagury, Roberto L., Antunes, Roberto A.

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