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R Tandan

Showing results (41-50 of 58) with videos related to

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Neurology|April 1, 1988
Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy)M D Mohire, R Tandan, T J Fries, et al.
Journal of the Neurological Sciences|December 1, 1987
Childhood giant axonal neuropathy. Case report and review of the literatureR Tandan, B W Little, E S Emery, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 2000
A Bethlem myopathy Gly to Glu mutation in the von Willebrand factor A domain N2 of the collagen alpha3(VI) chain interferes with protein foldingT Sasaki, E Hohenester, R Z Zhang, et al.
American Journal of Medical Genetics|August 28, 1995
Bethlem myopathy is not allelic to limb-girdle muscular dystrophy type 1AM C Speer, L H Yamaoka, J Stajich, et al.
Annals of Surgical Oncology|August 18, 2004
A prospective evaluation of positron emission tomography scanning, sentinel lymph node biopsy, and standard axillary dissection for axillary staging in patients with early stage breast cancerPeter J Lovrics, Vicky Chen, Geoff Coates, et al.
Neurology|November 1, 1996
A controlled trial of amino acid therapy in amyotrophic lateral sclerosis: I. Clinical, functional, and maximum isometric torque dataR Tandan, M B Bromberg, D Forshew, et al.
Journal of the Neurological Sciences|August 1, 1989
Quantitative measures of neurological function in chronic neuromuscular diseases and ataxiaM J Fillyaw, G J Badger, W G Bradley, et al.
Neurology|November 1, 1988
Double-blind controlled trials of Cronassial in chronic neuromuscular diseases and ataxiaW G Bradley, G J Badger, R Tandan, et al.
Progress in Clinical and Biological Research|January 1, 1989
DNA repair deficiency for alkylation damage in cells from Alzheimer's disease patientsW G Bradley, R J Polinsky, W W Pendlebury, et al.
Human Molecular Genetics|May 23, 1998
Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathyT C Pan, R Z Zhang, M A Pericak-Vance, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Neurology|April 1, 1988
Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy)M D Mohire, R Tandan, T J Fries, et al.
Journal of the Neurological Sciences|December 1, 1987
Childhood giant axonal neuropathy. Case report and review of the literatureR Tandan, B W Little, E S Emery, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 2000
A Bethlem myopathy Gly to Glu mutation in the von Willebrand factor A domain N2 of the collagen alpha3(VI) chain interferes with protein foldingT Sasaki, E Hohenester, R Z Zhang, et al.
American Journal of Medical Genetics|August 28, 1995
Bethlem myopathy is not allelic to limb-girdle muscular dystrophy type 1AM C Speer, L H Yamaoka, J Stajich, et al.
Annals of Surgical Oncology|August 18, 2004
A prospective evaluation of positron emission tomography scanning, sentinel lymph node biopsy, and standard axillary dissection for axillary staging in patients with early stage breast cancerPeter J Lovrics, Vicky Chen, Geoff Coates, et al.
Neurology|November 1, 1996
A controlled trial of amino acid therapy in amyotrophic lateral sclerosis: I. Clinical, functional, and maximum isometric torque dataR Tandan, M B Bromberg, D Forshew, et al.
Journal of the Neurological Sciences|August 1, 1989
Quantitative measures of neurological function in chronic neuromuscular diseases and ataxiaM J Fillyaw, G J Badger, W G Bradley, et al.
Neurology|November 1, 1988
Double-blind controlled trials of Cronassial in chronic neuromuscular diseases and ataxiaW G Bradley, G J Badger, R Tandan, et al.
Progress in Clinical and Biological Research|January 1, 1989
DNA repair deficiency for alkylation damage in cells from Alzheimer's disease patientsW G Bradley, R J Polinsky, W W Pendlebury, et al.
Human Molecular Genetics|May 23, 1998
Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathyT C Pan, R Z Zhang, M A Pericak-Vance, et al.
Pageof 6