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Neurology. Genetics|August 6, 2020
Expanded genetic insight and clinical experience of DNMT1-complex disorderHongyan Bi, Kaori Hojo, Masashi Watanabe, et al.
Neurology. Genetics|August 6, 2020
SLC12A2 mutations cause NKCC1 deficiency with encephalopathy and impaired secretory epitheliaTommy Stödberg, Måns Magnusson, Nicole Lesko, et al.
Neurology. Genetics|April 20, 2023
Novel Homozygous Variant in COQ7 in Siblings With Hereditary Motor NeuropathyIan C Smith, Chantal A Pileggi, Ying Wang, et al.
Neurology. Genetics|August 18, 2020
Delineating the phenotypic spectrum of sulfite oxidase and molybdenum cofactor deficiencyAlbert L Misko, Ye Liang, Joshua B Kohl, et al.
Neurology. Genetics|August 18, 2020
Genetic risk scores and hallucinations in patients with Parkinson diseaseCynthia D J Kusters, Kimberly C Paul, Aline Duarte Folle, et al.
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Neurology. Genetics|August 18, 2020
LINS1-associated neurodevelopmental disorder: Family with novel mutation expands the phenotypic spectrumChristiane M Neuhofer, Claudia B Catarino, Heinrich Schmidt, et al.
Neurology. Genetics|April 22, 2021
African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic VariantsSuzanne E Schindler, Carlos Cruchaga, Amulya Joseph, et al.
Neurology. Genetics|June 26, 2020
Prevalence of RFC1-mediated spinocerebellar ataxia in a North American ataxia cohortDona Aboud Syriani, Darice Wong, Sameer Andani, et al.
Neurology. Genetics|November 22, 2019
A family with spinocerebellar ataxia and retinitis pigmentosa attributed to an ELOVL4 mutationChangrui Xiao, Elaine M Binkley, Jessica Rexach, et al.
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