Showing results (51-60 of 61) with videos related to
Sort By:
Pageof 7
Annals of Clinical and Translational Neurology|June 24, 2026
Clinical and Modifiable Factors Associated With Disability and Relapse in MOGAD: A Multicentre Cohort StudyYingtao Wang, Shaoxin Tao, Qiujia Wang, et al.Nature Communications|October 2, 2025
Platelet activation plays a pro-inflammatory role in myasthenia gravisQi Wen, Shu Zhang, Yaye Wang, et al.Nature Communications|January 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humansClaudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig, et al.Nature|April 21, 2022
Somatic mosaicism reveals clonal distributions of neocortical developmentMartin W Breuss, Xiaoxu Yang, Johannes C M Schlachetzki, et al.JAMA Neurology|January 21, 2025
Novel Meningoencephalomyelitis Associated With Vimentin IgG AutoantibodiesDongshan Wan, Shufang Zhao, Chen Zhang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2020
Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative conditionShereen G Ghosh, Sangmoon Lee, Rudy Fabunan, et al.The New England Journal of Medicine|September 29, 2021
A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt SecretionGuoliang Chai, Emmanuelle Szenker-Ravi, Changuk Chung, et al.American Journal of Human Genetics|November 4, 2017
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and OsteopeniaThi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn Sheridan, et al.American Journal of Human Genetics|August 14, 2018
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia SyndromeShereen G Ghosh, Kerstin Becker, He Huang, et al.Neuron|November 21, 2020
Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with MicrocephalyGuoliang Chai, Alice Webb, Chen Li, et al.Pageof 7