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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|February 3, 2004
The genetics of motor neuron diseasesDenise A Figlewicz, Richard W OrrellCerebrovascular Diseases (Basel, Switzerland)|January 13, 2005
Coagulation factor XIII VaI34Leu polymorphism in patients with small vessel disease or primary intracerebral hemorrhageAgnieszka Slowik, Tomasz Dziedzic, Joanna Pera, et al.Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|December 24, 2002
Synergistic effects of low level stressors in an oxidative damage model of spinal motor neuron degenerationElizabeth Kriscenski-Perry, Heather D Durham, Shey-Shing Sheu, et al.Archives of Neurology|February 15, 2002
Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegiaInge A Meijer, Collette K Hand, P Cossette, et al.Biochemical and Biophysical Research Communications|September 1, 2009
Reduction of a 4q35-encoded nuclear envelope protein in muscle differentiationCecilia Ostlund, Tinglu Guan, Denise A Figlewicz, et al.Journal of Neurochemistry|March 5, 2008
Proteasomes remain intact, but show early focal alteration in their composition in a mouse model of amyotrophic lateral sclerosisEdor Kabashi, Jeffrey N Agar, Yu Hong, et al.Stroke|May 29, 2004
II genotype of the angiotensin-converting enzyme gene increases the risk for subarachnoid hemorrhage from ruptured aneurysmAgnieszka Slowik, Anna Borratynska, Joanna Pera, et al.Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 7, 2002
Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stressMark R Cookson, Fiona M Menzies, Philip Manning, et al.Stroke|June 5, 2004
A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in malesAgnieszka Slowik, Tomasz Dziedzic, Wojciech Turaj, et al.Stroke|February 19, 2005
Alpha1-antichymotrypsin gene (SERPINA3) A/T polymorphism as a risk factor for aneurysmal subarachnoid hemorrhageAgnieszka Slowik, Anna Borratynska, Wojciech Turaj, et al.Pageof 2