Waardenburg syndrome: Clinical differentiation between types I and II von Pardono, Eliete, van Bever, Yolande, van den Ende, Jenneke, Havrenne, Poti C., Iughetti, Paula, Maestrelli, Sylvia R.P., Costa F, Orozimbo, Richieri-Costa, Antonio, Frota-Pessoa, Oswaldo, Otto, Paulo A.

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Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant von Pardono, Eliete, Mazzeu, Juliana F., Lezirovitz, Karina, Auricchio, Maria Teresa B.M., Iughetti, Paula, Nascimento, Rafaella M.P., Mingroni-Netto, Regina C., Otto, Paulo A.

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Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17 von Nitrini, R, Teixeira da Silva, L S, Rosemberg, S, Caramelli, P, Carrilho, P E, Iughetti, P, Passos-Bueno, M R, Zatz, M, Albrecht, S, LeBlanc, A

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A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma von IUGHETTI, Paula, SUZUKI, Oscar, MOREIRA-FILHO, Carlos Alberto, SIMOSON, Andrew, OLIVA, Glaucius, PASSOS-BUENO, Maria Rita, GODOI, Paulo H. C, FERREIRA ALVES, Venancio Avancini, SERTIE, Andrea L, ZORICK, Todd, SOARES, Fernando, CAMARGO, Anamaria, MOREIRA, Eloisa S, DI LORETO, Celso

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Familial spongiform encephalopathy associated with a novel prion protein gene mutation von Nitrini, Ricardo, Rosemberg, Sergio, Passos-Bueno, Maria Rita, da Silva, Luís S. Teixeira, Iughetti, Paula, Papadopoulos, Maria, Carrilho, Paulo M., Caramelli, Paulo, Albrecht, Steffen, Zatz, Mayana, LeBlanc, Andrea

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Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasi... von Iughetti, Paula, Alonso, Luis Garcia, Wilcox, William, Alonso, Nivaldo, Passos-Bueno, Maria Rita

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Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region von Passos-Bueno, M.Rita, Bashir, Ramaisa, Moreira, Eloisa S., Vainzof, Mariz, Marie, Suely K., Vasquez, Luciana, Iughetti, Paula, Bakker, Egbert, Keers, Sharon, Stephenson, Anthea, Strachan, Tom, Mahneh, Ibrahim, Weissenbach, Jean, Bushby, Katharine, Zatz, Mayana

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Musca domestica hemolymph ferritin von Capurro, M. de L. (Universidade de Sao Paulo, Sao Paulo, SP, Brazil.), Iughetti, P, Ribolla, P.E.M, Bianchi, A.G. de

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Different behavior in the paternally vs. maternally inherited mutated allele in Brazilian Machado-Joseph (MJD1) Families von Iughetti, Paula, Otto, Paulo A., Zatz, Mayana, Bueno, Maria Rita Passos, Marie, Suely K.

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Progressive osseous heteroplasia: A case report with an unexpected trigger von Boncompagni, Alessandra, Lucas-Herald, Angela K., Beattie, Paula, McDevitt, Helen, Iughetti, Lorenzo, Constantinou, Panayiotis, Kinning, Esther, Ahmed, S. Faisal, Mason, Avril

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Progressive osseous heteroplasia: A case report with an unexpected trigger von Boncompagni, Alessandra, Lucas-Herald, Angela K, Beattie, Paula, McDevitt, Helen, Iughetti, Lorenzo, Constantinou, Panayiotis, Kinning, Esther, Ahmed, S Faisal, Mason, Avril

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