Showing results (741-750 of 823) with videos related to

Sort By:
Pageof 83
Journal of the American Society of Nephrology : JASN|May 9, 2020
ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid TreatmentEugen Widmeier, Seyoung Yu, Anish Nag, et al.
Neurology|September 4, 2016
Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndromeGina L O'Grady, Corien Verschuuren, Michaela Yuen, et al.
Neuromuscular Disorders : NMD|January 6, 2015
Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defectYiran Guo, Minal J Menezes, Manoj P Menezes, et al.
Brain : a Journal of Neurology|February 15, 2015
Expanding the phenotype of GMPPB mutationsMacarena Cabrera-Serrano, Roula Ghaoui, Gianina Ravenscroft, et al.
Neurology|November 2, 2022
Association Between Characteristics of National Association of Epilepsy Centers and Reported Utilization of Specific Surgical TechniquesKristen H Arredondo, Stephanie M Ahrens, Anto I Bagić, et al.
Elife|November 19, 2014
miR-142 regulates the tumorigenicity of human breast cancer stem cells through the canonical WNT signaling pathwayTaichi Isobe, Shigeo Hisamori, Daniel J Hogan, et al.
Epilepsia|November 1, 2022
Epilepsy center characteristics and geographic region influence presurgical testing in the United StatesStephanie M Ahrens, Kristen H Arredondo, Anto I Bagić, et al.
JAMA Neurology|October 6, 2015
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons LearnedRoula Ghaoui, Sandra T Cooper, Monkol Lek, et al.
Elife|March 21, 2022
Inhibiting USP16 rescues stem cell aging and memory in an Alzheimer's modelFelicia Reinitz, Elizabeth Y Chen, Benedetta Nicolis di Robilant, et al.
Chest|October 11, 2007
Multistate outbreak of Burkholderia cenocepacia colonization and infection associated with the use of intrinsically contaminated alcohol-free mouthwashPreeta K Kutty, Barbara Moody, Jessica Smartt Gullion, et al.
Pageof 83