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Annals of the New York Academy of Sciences|November 1, 2017
Mutation Testing in Charcot-Marie-Tooth NeuropathyGarth A NicholsonMuscle & Nerve|January 5, 2006
The dominantly inherited motor and sensory neuropathies: clinical and molecular advancesGarth A NicholsonBrain : a Journal of Neurology|May 13, 2008
Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosisSteve Vucic, Garth A Nicholson, Matthew C KiernanCell Cycle (Georgetown, Tex.)|March 9, 2004
Equilibrium between cell division and apoptosis in immortal cells as an alternative to the G1 restriction mechanism in mammalian cellsVadim N Dedov, Irina V Dedova, Garth A NicholsonCell Cycle (Georgetown, Tex.)|October 7, 2004
Hypoxia causes aggregation of serine palmitoyltransferase followed by non-apoptotic death of human lymphocytesVadim N Dedov, Irina V Dedova, Garth A NicholsonJournal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 20, 2010
Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathiesLana A del Porto, Garth A Nicholson, Pon KetheswarenMovement Disorders : Official Journal of the Movement Disorder Society|July 12, 2002
Friedreich's ataxia with chorea and myoclonus caused by a compound heterozygosity for a novel deletion and the trinucleotide GAA expansionDanqing Zhu, Christopher Burke, Anthony Leslie, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 19, 2013
Apparent anticipation in SOD1 familial amyotrophic lateral sclerosisSteve Vucic, Garth A Nicholson, Adriano Chio, et al.The International Journal of Biochemistry & Cell Biology|June 15, 2010
Fused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding proteinShu Yang, Sadaf T Warraich, Garth A Nicholson, et al.Neurogenetics|July 9, 2004
Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genesCindy Kok, Marina L Kennerson, Simon J Myers, et al.Pageof 10