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Seizure|August 13, 2024
Neurofilament light (NfL) concentrations in patients with epilepsy with recurrent isolated seizures: Insights from a clinical cohort studyJustina Dargvainiene, Safa Sahaf, Jeanette Franzenburg, et al.Movement Disorders Clinical Practice|September 5, 2024
Archimedes Spiral Ratings: Determinants and Population-Based Limits of NormalFranziska Hopfner, Anja Tietz, Yuri D'Elia, et al.Journal of Neurology|October 27, 2004
Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissectionsCarsten Konrad, Georg A Müller, Claus Langer, et al.Muscle & Nerve|March 31, 2004
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophyGert Hünermund, Anja Schirmacher, Bernd Ringelstein, et al.Heliyon|July 21, 2021
Atypical pantothenate kinase-associated neurodegeneration with variable phenotypes in an Egyptian familyAli S Shalash, Thomas W Rösler, Ibrahim Y Abdelrahman, et al.Journal of Child Neurology|November 22, 2013
Broad phenotypic heterogeneity due to a novel SCN1A mutation in a family with genetic epilepsy with febrile seizures plusHadassa Goldberg-Stern, Sharon Aharoni, Zaid Afawi, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
LINGO1 is not associated with Parkinson's disease in German patientsStephan Klebe, Sandra Thier, Delia Lorenz, et al.Neurology. Genetics|November 18, 2017
c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystoniaAli S Shalash, Thomas W Rösler, Stefanie H Müller, et al.American Journal of Human Genetics|January 21, 2010
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B geneSilke Appenzeller, Anja Schirmacher, Hartmut Halfter, et al.Journal of Neurology|October 14, 2015
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasiaKarl Martin Klein, Manuela Pendziwiat, Rony Cohen, et al.Pageof 10