Showing results (61-70 of 849) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|August 20, 2016
Rare disease clinical trials: Power in numbersMatthew P Wicklund
Neurology. Genetics|August 10, 2016
Complex relation of HLA-DRB1*1501, age at menarche, and age at multiple sclerosis onsetRiley Bove, Alicia S Chua, Zongqi Xia, et al.
Neurology. Genetics|August 10, 2016
Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer lociGail Chan, Charles C White, Phoebe A Winn, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Neurology. Genetics|March 1, 2017
Redefining the phenotype of ALSP and AARS2 mutation-related leukodystrophyRahul Lakshmanan, Matthew E Adams, David S Lynch, et al.
Neurology. Genetics|June 22, 2017
Previously unrecognized behavioral phenotype in Gaucher disease type 3Magy Abdelwahab, Michael Potegal, Elsa G Shapiro, et al.
Neurology. Genetics|September 21, 2016
Loss of MUNC13-1 function causes microcephaly, cortical hyperexcitability, and fatal myastheniaAndrew G Engel, Duygu Selcen, Xin-Ming Shen, et al.
Neurology. Genetics|August 2, 2018
Longitudinal analysis of contrast acuity in Friedreich ataxiaAli G Hamedani, Lauren A Hauser, Susan Perlman, et al.
Neurology. Genetics|May 17, 2017
Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial diseaseEnrico Bugiardini, Olivia V Poole, Andreea Manole, et al.
Neurology. Genetics|June 12, 2018
Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathyMarkus T Sainio, Emil Ylikallio, Laura Mäenpää, et al.
Pageof 85