Kết quả tìm kiếm - Jonas Alex Morales Saute
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Riluzole in patients with hereditary cerebellar ataxia Bằng Jonas Alex Morales Saute, Laura Bannach Jardim
Được phát hành 2016Carta -
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Challenges in quantifying ataxia in core and comorbid early onset ataxias Bằng Jonas Alex Morales Saute, Laura Bannach Jardim
Được phát hành 2016Carta -
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When ataxia is not just ataxia Bằng Christian Kieling, Jonas Alex Morales Saute, Laura Bannach Jardim
Được phát hành 2007Carta -
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Diagnostic reasoning in neurogenetics: a general approach Bằng Helena Fussiger, José Luiz Pedroso, Jonas Alex Morales Saute
Được phát hành 2022Revisão -
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Diagnostic reasoning in neurogenetics: a general approach Bằng Helena Fussiger, José Luiz Pedroso, Jonas Alex Morales Saute
Được phát hành 2023Conjunto de Dados -
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Simultaneous bilateral optic neuritis and longitudinally extensive transverse myelitis following vaccination against COVID-19: A case report Bằng Wyllians Vendramini Borelli, André Luís Marques da Silveira, Alessandro Finkelsztejn, Gisele Hansel, Douglas Kazutoshi Sato, Jonas Alex Morales Saute
Được phát hành 2021Artigo -
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Expanding the Diagnosis of Familial Dilated Cardiomyopathy among Heart Transplant Recipients with a Screening Instrument Bằng Laura Caroline Tavares Hastenteufel, Fernando Luís Scolari, F. Scussel, J. Brum, Th. Krebs, Jonas Alex Morales Saute, N. Clausell, Lívia Adams Goldraich
Được phát hành 2022Artigo -
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Co-Occurrence of Myotonic Dystrophy Type 1 and Limb-Girdle Muscular Dystrophy Type 2B: A Case Report Bằng Lucas Augusto Hauschild, Taciana Seixas Maia da Silva, Pablo Brea Winckler, Laércio Moreira Cardoso-Júnior, Jonas Alex Morales Saute, Karina Carvalho Donis
Được phát hành 2023Artigo -
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Long-term progression of clinician-reported and gait performance outcomes in hereditary spastic paraplegias Bằng Diana Maria Cubillos Arcila, Gustavo Dariva Machado, Valéria Feijó Martins, Vanessa Bielefeldt Leotti, Rebecca Schüle, Leonardo Alexandre Peyré‐Tartaruga, Jonas Alex Morales Saute
Được phát hành 2023Artigo -
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Cognitive profile of patients with facioscapulohumeral muscular dystrophy Bằng 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
Được phát hành 2021Artigo -
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Speech and swallowing characteristics in patients with facioscapulohumeral muscular dystrophy Bằng 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
Được phát hành 2022Artigo -
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Genotype-phenotype correlation of neurodevelopmental disorders in patients with dystrophinopathies Bằng 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
Được phát hành 2025Artigo -
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SPTLC1 variants associated with childhood onset amyotrophic lateral sclerosis produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins Bằng 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
Được phát hành 2022Pré-impressão -
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SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins Bằng 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
Được phát hành 2022Artigo -
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MR Imaging in Spinocerebellar Ataxias: A Systematic Review Bằng 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
Được phát hành 2016Revisão
Công cụ tìm kiếm:
Các môn học liên quan
Medicine
Internal medicine
Biology
Disease
Gene
Genetics
Pathology
Pediatrics
Psychology
Neuroscience
Psychiatry
Physical medicine and rehabilitation
Phenotype
Physical therapy
Ataxia
Cerebral palsy
Computer science
Hereditary spastic paraplegia
Muscular dystrophy
Mutation
Spastic
Spinocerebellar ataxia
Audiology
Biochemistry
Mathematics
Spinal muscular atrophy
Chemistry
Duchenne muscular dystrophy
Endocrinology
Environmental health