Showing results (191-200 of 409) with videos related to
Sort By:
Pageof 41
Neurology|August 23, 2013
Clinical and MRI activity as determinants of sample size for pediatric multiple sclerosis trialsLeonard H Verhey, Alessio Signori, Douglas L Arnold, et al.American Journal of Human Genetics|November 1, 2011
Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophyMartine Tétreault, Karine Choquet, Simona Orcesi, et al.Journal of Proteome Research|April 26, 2008
Time series proteome profiling to study endoplasmic reticulum stress responseMichelle Mintz, Adeline Vanderver, Kristy J Brown, et al.Neurology|May 3, 2019
Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSGEmmanuelle Waubant, Brenda Banwell, Evangeline Wassmer, et al.BMJ Neurology Open|March 21, 2022
Effect of fingolimod on health-related quality of life in paediatric patients with multiple sclerosis: results from the phase 3 PARADIGMS StudyLauren Krupp, Brenda Banwell, Tanuja Chitnis, et al.Molecular Genetics and Metabolism Reports|December 22, 2021
Corrigendum to "Long-term follow-up of renal function in patients treated with migalastat for Fabry disease" [Bichet et al., MGM Reports; 28 (2021) 100786]Daniel G Bichet, Roser Torra, Eric Wallace, et al.Pediatric Research|February 22, 2003
Myoclonic epilepsy in Gaucher disease: genotype-phenotype insights from a rare patient subgroupJoseph K Park, Eduard Orvisky, Nahid Tayebi, et al.BMC Neurology|November 8, 2008
Skin-impedance in Fabry Disease: a prospective, controlled, non-randomized clinical studySurya N Gupta, Markus Ries, Gary J Murray, et al.Molecular Genetics and Metabolism Reports|August 17, 2021
Long-term follow-up of renal function in patients treated with migalastat for Fabry diseaseDaniel G Bichet, Roser Torra, Eric Wallace, et al.Annals of Neurology|September 27, 2002
Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locusAnne Fogli, Kondi Wong, Eleonore Eymard-Pierre, et al.Pageof 41