Хайлтын үр дүнгүүд - Jonas Alex Morales Saute
- 66-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Diagnostic reasoning in neurogenetics: a general approach -н Helena Fussiger, José Luiz Pedroso, Jonas Alex Morales Saute
Хэвлэсэн 2023Conjunto de Dados -
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Simultaneous bilateral optic neuritis and longitudinally extensive transverse myelitis following vaccination against COVID-19: A case report -н Wyllians Vendramini Borelli, André Luís Marques da Silveira, Alessandro Finkelsztejn, Gisele Hansel, Douglas Kazutoshi Sato, Jonas Alex Morales Saute
Хэвлэсэн 2021Artigo -
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Expanding the Diagnosis of Familial Dilated Cardiomyopathy among Heart Transplant Recipients with a Screening Instrument -н Laura Caroline Tavares Hastenteufel, Fernando Luís Scolari, F. Scussel, J. Brum, Th. Krebs, Jonas Alex Morales Saute, N. Clausell, Lívia Adams Goldraich
Хэвлэсэн 2022Artigo -
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Long-term progression of clinician-reported and gait performance outcomes in hereditary spastic paraplegias -н Diana Maria Cubillos Arcila, Gustavo Dariva Machado, Valéria Feijó Martins, Vanessa Bielefeldt Leotti, Rebecca Schüle, Leonardo Alexandre Peyré‐Tartaruga, Jonas Alex Morales Saute
Хэвлэсэн 2023Artigo -
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Cognitive profile of patients with facioscapulohumeral muscular dystrophy -н 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
Хэвлэсэн 2021Artigo -
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Speech and swallowing characteristics in patients with facioscapulohumeral muscular dystrophy -н 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
Хэвлэсэн 2022Artigo -
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Genotype-phenotype correlation of neurodevelopmental disorders in patients with dystrophinopathies -н 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
Хэвлэсэн 2025Artigo -
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SPTLC1 variants associated with childhood onset amyotrophic lateral sclerosis produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins -н 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
Хэвлэсэн 2022Pré-impressão -
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SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins -н 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
Хэвлэсэн 2022Artigo -
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MR Imaging in Spinocerebellar Ataxias: A Systematic Review -н 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
Хэвлэсэн 2016Revisão
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
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