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G A Nicholson

Showing results (101-110 of 115) with videos related to

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Journal of Human Hypertension|February 13, 2004
AGT and RH blood group polymorphisms affect blood pressure and lipids in Afro-CaribbeansM T Robinson, T W Wilson, G A Nicholson, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Clinical Genetics|January 21, 2017
The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in AustraliaE P McCann, K L Williams, J A Fifita, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxiaE Storey, D du Sart, J H Shaw, et al.
Journal of the Neurological Sciences|November 1, 1979
An evaluation of some carrier detection techniques in Duchenne muscular dystrophyR J Lane, P Maskrey, G A Nicholson, et al.
Neuroscience Letters|October 27, 1995
A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's diseaseW S Brooks, R N Martins, J De Voecht, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 13, 2016
Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathyN Shahrizaila, Y Noto, N G Simon, et al.
Experimental Neurology|May 1, 1989
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17J M Vance, G A Nicholson, L H Yamaoka, et al.
Nature Genetics|March 1, 1994
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesG A Nicholson, L J Valentijn, A K Cherryson, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Journal of Human Hypertension|February 13, 2004
AGT and RH blood group polymorphisms affect blood pressure and lipids in Afro-CaribbeansM T Robinson, T W Wilson, G A Nicholson, et al.
Neurology|May 5, 1998
Charcot-Marie-Tooth disease and Noonan syndrome with giant proximal nerve hypertrophyP A Silburn, G A Nicholson, B T Teh, et al.
Clinical Genetics|January 21, 2017
The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in AustraliaE P McCann, K L Williams, J A Fifita, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxiaE Storey, D du Sart, J H Shaw, et al.
Journal of the Neurological Sciences|November 1, 1979
An evaluation of some carrier detection techniques in Duchenne muscular dystrophyR J Lane, P Maskrey, G A Nicholson, et al.
Neuroscience Letters|October 27, 1995
A mutation in codon 717 of the amyloid precursor protein gene in an Australian family with Alzheimer's diseaseW S Brooks, R N Martins, J De Voecht, et al.
American Journal of Medical Genetics|October 26, 1999
Clinical and genetic study of Friedreich ataxia in an Australian populationM B Delatycki, D B Paris, R J Gardner, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 13, 2016
Quantitative muscle ultrasound as a biomarker in Charcot-Marie-Tooth neuropathyN Shahrizaila, Y Noto, N G Simon, et al.
Experimental Neurology|May 1, 1989
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17J M Vance, G A Nicholson, L H Yamaoka, et al.
Nature Genetics|March 1, 1994
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiesG A Nicholson, L J Valentijn, A K Cherryson, et al.
Pageof 12