Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Journal of Chromatographic Science|July 9, 2025
Simple, Sensitive and Reproducible High-performance Liquid Chromatographic Method for Determination of Mixed Tocotrienol in Blood Plasma using Fluorescent DetectionTeong G Thor, Song T Goh, Kah H Yuen, et al.
Glycoconjugate Journal|December 1, 1992
Use of large-scale hydrazinolysis in the preparation of N-linked oligosaccharide libraries: application to brain tissueD R Wing, T W Rademacher, M C Field, et al.
Neuromuscular Disorders : NMD|March 7, 2017
Congenital myopathy with "corona" fibres, selective muscle atrophy, and craniosynostosis associated with novel recessive mutations in SCN4AHernan D Gonorazky, Christian R Marshall, Maryam Al-Murshed, et al.
Scientific Reports|November 28, 2019
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutationMichael G Thor, Vinojini Vivekanandam, Marisol Sampedro-Castañeda, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2018
Spider toxin inhibits gating pore currents underlying periodic paralysisRoope Männikkö, Zakhar O Shenkarev, Michael G Thor, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Brain : a Journal of Neurology|December 25, 2015
Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathyIrina T Zaharieva, Michael G Thor, Emily C Oates, et al.
Pageof 2