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Garth Nicholson

Showing results (11-20 of 67) with videos related to

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The Australian Journal of Physiotherapy|September 1, 2006
Night splinting does not increase ankle range of motion in people with Charcot-Marie-Tooth disease: a randomised, cross-over trialKathryn M Refshauge, Jacqueline Raymond, Garth Nicholson, et al.
Clinical Neurology and Neurosurgery|November 8, 2005
Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findingsAndrea J Lindahl, Sam D Lhatoo, Malcolm J Campbell, et al.
Neurogenetics|May 7, 2008
Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb regionMegan Brewer, Febriani Changi, Anthony Antonellis, et al.
Neurogenetics|May 23, 2003
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the regionDanqing Zhu, Marina Kennerson, John Merory, et al.
Muscle & Nerve|September 8, 2017
Sarcolemmal excitability in the myotonic dystrophiesRobert Boland-Freitas, James Lee, James Howells, et al.
Muscle & Nerve|April 5, 2013
Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutationRabia Chaudhry, Aditi Kidambi, Megan Hwa Brewer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2018
A novel Parkinson's disease risk variant, p. W378R, in the Gaucher's disease GBA geneMichal Lubomski, Michael Hayes, Marina Kennerson, et al.
Neurogenetics|March 6, 2010
X-linked CMT: genes and gene loci in an Australian cohortMegan Hwa Brewer, Rabia Chaudhry, Keta McDowall, et al.
Journal of the Peripheral Nervous System : JPNS|October 5, 2016
Relationship between physical performance and quality of life in Charcot-Marie-Tooth disease: a pilot studyDaniel Roberts-Clarke, Che Fornusek, Nidhi Saigal, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
The Australian Journal of Physiotherapy|September 1, 2006
Night splinting does not increase ankle range of motion in people with Charcot-Marie-Tooth disease: a randomised, cross-over trialKathryn M Refshauge, Jacqueline Raymond, Garth Nicholson, et al.
Clinical Neurology and Neurosurgery|November 8, 2005
Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findingsAndrea J Lindahl, Sam D Lhatoo, Malcolm J Campbell, et al.
Neurogenetics|May 7, 2008
Evidence of a founder haplotype refines the X-linked Charcot-Marie-Tooth (CMTX3) locus to a 2.5 Mb regionMegan Brewer, Febriani Changi, Anthony Antonellis, et al.
Neurogenetics|May 23, 2003
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the regionDanqing Zhu, Marina Kennerson, John Merory, et al.
Muscle & Nerve|September 8, 2017
Sarcolemmal excitability in the myotonic dystrophiesRobert Boland-Freitas, James Lee, James Howells, et al.
Muscle & Nerve|April 5, 2013
Re-analysis of an original CMTX3 family using exome sequencing identifies a known BSCL2 mutationRabia Chaudhry, Aditi Kidambi, Megan Hwa Brewer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2018
A novel Parkinson's disease risk variant, p. W378R, in the Gaucher's disease GBA geneMichal Lubomski, Michael Hayes, Marina Kennerson, et al.
Neurogenetics|March 6, 2010
X-linked CMT: genes and gene loci in an Australian cohortMegan Hwa Brewer, Rabia Chaudhry, Keta McDowall, et al.
Journal of the Peripheral Nervous System : JPNS|October 5, 2016
Relationship between physical performance and quality of life in Charcot-Marie-Tooth disease: a pilot studyDaniel Roberts-Clarke, Che Fornusek, Nidhi Saigal, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Pageof 7