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Arthur J. Hudson
University of Western Ontario
40Publications
16H-index
1,448Citations
Publications 40
Newest
1 CitationsSource
#1Arthur J. Hudson (UWO: University of Western Ontario)H-Index: 16
#2David G. Munoz (UWO: University of Western Ontario)H-Index: 54
Last.Fred H. Gage (Salk Institute for Biological Studies)H-Index: 195
view all 6 authors...
#1Arthur J. Hudson (UWO: University of Western Ontario)H-Index: 16
#2David G. Munoz (UWO: University of Western Ontario)H-Index: 54
1 CitationsSource
#1Arthur J. HudsonH-Index: 16
#2David G. MunozH-Index: 54
Last.Fred H. GageH-Index: 195
view all 6 authors...
#1Arthur J. Hudson (UWO: University of Western Ontario)H-Index: 16
Bien que des etudes effectuees au cours des dernieres decennies aient decrit de facon detaillee les voies nociceptives peripheriques et ascendantes vers le thalamus et le cortex cerebral, la douleur est demeuree un symptome difficile a caracteriser au point de vue anatomique et physiologique. La tomographie par l'emission de positons et l'imagerie par resonance magnetique fonctionnelle ont demontre recemment l'existence d'un certain nombre de sites qui repondent a des stimuli cutanes desagreable...
56 CitationsSource
Source
#1Arthur J. Hudson (UWO: University of Western Ontario)H-Index: 16
#2David G. Munoz (UWO: University of Western Ontario)H-Index: 54
We present a family with congenital cataract with, in some cases, mental retardation and emotional instability, but intellectual deterioration in all affected members. The latter was accompanied by psychosis in some. The inheritance is most likely autosomal dominant, affecting two generations and consisting of a congenitally blind parent and 6 of 11 of her offspring. In addition to these features, some affected individuals had dysphagia and movement disorder, especially choreiform movements. The...
6 CitationsSource
#1Arthur J. HudsonH-Index: 16
#2George C. EbersH-Index: 85
Last.Dennis E. BulmanH-Index: 42
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The cause of several familial muscular diseases have recently been linked to mutations within skeletal muscle sodium and chloride channel genes. Thomsen's and Becker's diseases are autosomal dominant and recessive, respectively, and are caused by at least seven different mutations in the CLCNI (ClC-1) skeletal muscle chloride channel gene on chromosome 7q35. Hyperkalaemic periodic paralysis, paramyotonia congenita and a small heterogeneous group of related pure myotonias are autosomal dominant d...
85 CitationsSource
#1Dennis E. BulmanH-Index: 42
#2L L TollarH-Index: 1
Last.George C. EbersH-Index: 85
view all 7 authors...
#1Dennis E. BulmanH-Index: 42
#2L L TollarH-Index: 1
Last.George C. EbersH-Index: 85
view all 8 authors...
1 Citations
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