Search Results - Jonas Alex Morales Saute
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When ataxia is not just ataxia by Christian Kieling, Jonas Alex Morales Saute, Laura Bannach Jardim
Published 2007Carta -
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Diagnostic reasoning in neurogenetics: a general approach by Helena Fussiger, José Luiz Pedroso, Jonas Alex Morales Saute
Published 2022Revisão -
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Diagnostic reasoning in neurogenetics: a general approach by Helena Fussiger, José Luiz Pedroso, Jonas Alex Morales Saute
Published 2023Conjunto de Dados -
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Simultaneous bilateral optic neuritis and longitudinally extensive transverse myelitis following vaccination against COVID-19: A case report by Wyllians Vendramini Borelli, André Luís Marques da Silveira, Alessandro Finkelsztejn, Gisele Hansel, Douglas Kazutoshi Sato, Jonas Alex Morales Saute
Published 2021Artigo -
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Expanding the Diagnosis of Familial Dilated Cardiomyopathy among Heart Transplant Recipients with a Screening Instrument by Laura Caroline Tavares Hastenteufel, Fernando Luís Scolari, F. Scussel, J. Brum, Th. Krebs, Jonas Alex Morales Saute, N. Clausell, Lívia Adams Goldraich
Published 2022Artigo -
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Long-term progression of clinician-reported and gait performance outcomes in hereditary spastic paraplegias by Diana Maria Cubillos Arcila, Gustavo Dariva Machado, Valéria Feijó Martins, Vanessa Bielefeldt Leotti, Rebecca Schüle, Leonardo Alexandre Peyré‐Tartaruga, Jonas Alex Morales Saute
Published 2023Artigo -
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Speech and swallowing characteristics in patients with facioscapulohumeral muscular dystrophy by Vanessa Brzoskowski dos Santos, Jonas Alex Morales Saute, Laís Alves Jacinto-Scudeiro, A. Jean Ayres, Rafaela Soares Rech, Alcyr Alves de Oliveira, Maira Rozenfeld Olchik
Published 2022Artigo -
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Genotype-phenotype correlation of neurodevelopmental disorders in patients with dystrophinopathies by Félix Alexandre Antunes Soares, Bruna Faria Rosa, G Giordani, Daniela Mayumi Usuda Prado Rocha, Ana Carolina Brusius-Facchin, Michele M Becker, Jonas Alex Morales Saute
Published 2025Artigo -
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SPTLC1 variants associated with childhood onset amyotrophic lateral sclerosis produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins by Museer A. Lone, Mari J. Aaltonen, Aliza Zidell, Hélio Pedro, Jonas Alex Morales Saute, Shalett Mathew, Payam Mohassel, Carsten G. Bönnemann, Eric A. Shoubridge, Thorsten Hornemann
Published 2022Pré-impressão -
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SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins by Museer A. Lone, Mari J. Aaltonen, Aliza Zidell, Hélio Pedro, Jonas Alex Morales Saute, Shalett Mathew, Payam Mohassel, Carsten G. Bönnemann, Eric A. Shoubridge, Thorsten Hornemann
Published 2022Artigo -
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MR Imaging in Spinocerebellar Ataxias: A Systematic Review by Amália Izaura Nair de Medeiros Klaes, Estela Da Rosa Reckziegel, Marcondes C. França, Thiago Junqueira Ribeiro de Rezende, Leonardo Vedolin, Laura Bannach Jardim, Jonas Alex Morales Saute
Published 2016Revisão
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