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Journal of Neurology|May 16, 2015
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxiaM J Keogh, H Steele, K Douroudis, et al.Journal of Neurology|May 16, 2015
Functional neural substrates of posterior cortical atrophy patientsH Shames, N Raz, Netta LevinJournal of Neurology|May 6, 2020
Persistent asymptomatic or mild symptomatic hyperCKemia due to mutations in ANO5: the mildest end of the anoctaminopathies spectrumLuísa Panadés-de Oliveira, Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, et al.Journal of Neurology|May 8, 2020
Correction to: Endovascular stroke treatment's impact on malignant type of edema (ESTIMATE)Hannah Fuhrer, Silvia Schönenberger, Wolf-Dirk Niesen, et al.Journal of Neurology|May 10, 2020
Application of "Mentzer's PML case definition" to natalizumab-treated patients in the setting of strict MRI-based pharmacovigilanceMartijn T Wijburg, Clemens Warnke, Joep Killestein, et al.Journal of Neurology|May 11, 2020
Cerebellar degeneration in adult spinal muscular atrophy patientsFabrício Castro de Borba, Giorgia Querin, Marcondes Cavalcante França, et al.Journal of Neurology|May 13, 2020
Asymmetry index of Blink Reflex Recovery Cycle differentiates Parkinson's disease from atypical Parkinsonian syndromesGiorgia Sciacca, Giovanni Mostile, Ivano Disilvestro, et al.Journal of Neurology|May 4, 2020
Whole-body muscle MRI of patients with MATR3-associated distal myopathy reveals a distinct pattern of muscular involvement and highlights the value of whole-body examinationAlexander Mensch, Torsten Kraya, Felicitas Koester, et al.Journal of Neurology|May 9, 2020
Advantages of timing the duration of a freezing of gait-provoking test in individuals with Parkinson's diseaseTalia Herman, Moria Dagan, Shirley Shema-Shiratzky, et al.Journal of Neurology|December 24, 1997
Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year periodE M Hoogerwaard, W G de Voogt, A A Wilde, et al.Pageof 1,106