Rett syndrome: clinical and molecular characterization of two Brazilian patients Síndrome de Rett: caracterização clínica e molecular de dois casos brasileiros by Andrea Stachon, Francisco Baptista Assumpção Jr, Salmo Raskin

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Juvenile Huntington's disease confirmed by genetic examination in twins Doença de Huntington juvenil confirmada por exame genético em gêmeas by GILBERTO LEVY, MARIA EDUARDA NOBRE, VINICIUS T. CIMINI, SALMO RASKIN, ELIASZ ENGELHARDT

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Spinocerebellar ataxia type 6 in Brazil Ataxia espinocerebelar tipo 6 no Brasil by Hélio A.G. Teive, Renato Puppi Munhoz, Salmo Raskin, Lineu César Werneck

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Migrânea com afasia: relato de uma família by DANIEL BENZECRY ALMEIDA, WALTER OLESCHKO ARRUDA, RICARDO RAMINA, ARI ANTÔNIO PEDROZO, SALMO RASKIN

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Evidence and practices of the use of next generation sequencing in patients with undiagnosed autosomal dominant cerebellar ataxias: a review by Luiz Eduardo NOVIS, Mariana SPITZ, Marcia JARDIM, Salmo RASKIN, Hélio A. G. TEIVE

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The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene A história da ataxia espinocerebelar tipo 10 no Brasil: as viagens de um gene by Hélio A.G. Teive, Walter O. Arruda, Salmo Raskin, Tetsuo Ashizawa, Lineu César Werneck

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Clinical relevance of "bulging eyes" for the differential diagnosis of spinocerebellar ataxias by Adriana Moro, Renato Puppi Munhoz, Walter Oleschko Arruda, Salmo Raskin, Helio Afonso Ghizoni Teive

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Non-choreic movement disorders as initial manifestations of Huntington's disease Distúrbios do movimento não-coreicos como manifestação inicial da doença de Huntington by Nilson Becker, Renato P. Munhoz, Salmo Raskin, Lineu César Werneck, Hélio A.G. Teive

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Spinocerebellar ataxia type 3: subphenotypes in a cohort of brazilian patients by Adriana Moro, Renato P. Munhoz, Walter O. Arruda, Salmo Raskin, Mariana Moscovich, Hélio A.G. Teive

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Deletion Involving the 7q31-32 Band at the CADPS2 Gene Locus in a Patient with Autism Spectrum Disorder and Recurrent Psychotic Syndrome Triggered by Stress by Paulo André Pera Grabowski, Alexandre Ferreira Bello, Diogo Lima Rodrigues, Murilo José Forbeci, Vinicius Motter, Salmo Raskin

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Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystonia by Carlos Henrique F. Camargo, Sarah Teixeira Camargos, Salmo Raskin, Francisco Eduardo C. Cardoso, Hélio Afonso G. Teive

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Congenital contractural arachnodactyly with neurogenic muscular atrophy: case report by Rosana Herminia Scola, Lineu Cesar Werneck, Fabio Massaiti Iwamoto, Letícia Cristine Ribas, Salmo Raskin, Ylmar Correa Neto

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Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids by Adriana Moro, Renato P. Munhoz, Salmo Raskin, Torben C. Bezerra, Mariana Moscovich, Tetsuo Ashizawa, Hélio A.G. Teive

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Acute onset of cerebellar ataxia in a spinocerebellar ataxia type 10 patient after use of steroids Início agudo de ataxia cerebelar em paciente com ataxia espinocerebelar tipo 10 a... by Adriana Moro, Renato P. Munhoz, Salmo Raskin, Torben C. Bezerra, Mariana Moscovich, Tetsuo Ashizawa, Hélio A.G. Teive

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Rigid spine syndrome: case report by VIVIANE H. FLUMIGNAN ZÉTOLA, ROSANA HERMÍNIA SCOLA, SALMO RASKIN, DANIEL MONTE SERRAT PREVENDELLO, YLMAR CORREA NETO, LINEU CESAR WERNECK

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Kennedy's disease phenotype with positive genetic study for Kugelberg-Welander's disease: case report Fenótipo de doença de Kennedy com estudo genético positivo para doença de Kuge... by Ana P. Trentin, Rosana H. Scola, Hélio A.G. Teive, Salmo Raskin, Francisco M.B. Germiniani, Lineu C. Werneck

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Itajaí, Santa Catarina – Azorean ancestry and spinocerebellar ataxia type 3 by Hélio A. G. Teive, Adriana Moro, Walter O. Arruda, Salmo Raskin, Gladys M. G. Teive, Norberto Dallabrida, Renato P. Munhoz

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Epileptic encephalopathy and atypical Rett syndrome with mutations in CDKL5: clinical and molecular characterization of two Brazilian patients by Erica Leitao Ermel, Lauriane Caroline Carneiro, Carolina Fischinger Moura de Souza, Ana Chrystina de Souza Crippa, Maria Teresa Vieira Sanseverino, Salmo Raskin

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Cervical dystonia: about familial and sporadic cases in 88 patients by Carlos Henrique F. Camargo, Sarah Teixeira Camargos, Nilson Becker, Renato Puppi Munhoz, Salmo Raskin, Francisco Eduardo C. Cardoso, Hélio Afonso G. Teive

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Atrofia muscular bulbo espinhal recessiva ligada ao cromossomo X (doença de Kennedy): estudo de uma família by DAMACIO RAMÓN KAIMEN-MACIEL, MILTON MEDEIROS, VALTER CLÍMACO, GIORGE RIBEIRO KELIAN, LUIS SIDONIO TEIXEIRA DA SILVA, MÔNICA MARCOS DE SOUZA, SALMO RASKIN

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