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R C Griggs

Showing results (61-70 of 191) with videos related to

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Neurology|August 1, 1979
Regulation of plasma potassium in hyperkalemic periodic paralysisE D Lewis, R C Griggs, R T Moxley
Neurology|December 1, 1980
3-methylhistidine excretion in myotonic dystrophyR C Griggs, R T Moxley, G B Forbes
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Episodic movement disorders as channelopathiesK P Bhatia, R C Griggs, L J Ptácek
Annals of Internal Medicine|February 1, 1977
Acetazolamide-induced weakness in paramyotonia congenitaJ E Riggs, R C Griggs, R T Moxley
Archives of Neurology|October 1, 1985
Severe neonatal centronuclear myopathy with autosomal dominant inheritanceC F Torres, R C Griggs, J P Goetz
Archives of Neurology|January 1, 1984
Dissociation of glucose and potassium arterial-venous differences across the forearm by acetazolamide. A possible relationship to acetazolamide's beneficial effect in hypokalemic periodic paralysisJ E Riggs, R C Griggs, R T Moxley
Archives of Neurology|July 1, 1984
Effect of acetazolamide on insulin sensitivity in myotonic disordersA Corbett, W Kingston, R C Griggs, et al.
Annals of Neurology|March 20, 1998
Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH ConsortiumR Tawil, D A Figlewicz, R C Griggs, et al.
Archives of Neurology|November 1, 1995
Scapuloperoneal syndromes. Absence of linkage to the 4q35 FSHD locusR Tawil, G J Myers, B Weiffenbach, et al.
Neurology|November 1, 1993
Intranuclear rods in severe congenital nemaline myopathyZ Rifai, A M Kazee, C Kamp, et al.
Pageof 20

Showing results (61-70 of 191) with videos related to

Sort By:
Pageof 20
Neurology|August 1, 1979
Regulation of plasma potassium in hyperkalemic periodic paralysisE D Lewis, R C Griggs, R T Moxley
Neurology|December 1, 1980
3-methylhistidine excretion in myotonic dystrophyR C Griggs, R T Moxley, G B Forbes
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Episodic movement disorders as channelopathiesK P Bhatia, R C Griggs, L J Ptácek
Annals of Internal Medicine|February 1, 1977
Acetazolamide-induced weakness in paramyotonia congenitaJ E Riggs, R C Griggs, R T Moxley
Archives of Neurology|October 1, 1985
Severe neonatal centronuclear myopathy with autosomal dominant inheritanceC F Torres, R C Griggs, J P Goetz
Archives of Neurology|January 1, 1984
Dissociation of glucose and potassium arterial-venous differences across the forearm by acetazolamide. A possible relationship to acetazolamide's beneficial effect in hypokalemic periodic paralysisJ E Riggs, R C Griggs, R T Moxley
Archives of Neurology|July 1, 1984
Effect of acetazolamide on insulin sensitivity in myotonic disordersA Corbett, W Kingston, R C Griggs, et al.
Annals of Neurology|March 20, 1998
Facioscapulohumeral dystrophy: a distinct regional myopathy with a novel molecular pathogenesis. FSH ConsortiumR Tawil, D A Figlewicz, R C Griggs, et al.
Archives of Neurology|November 1, 1995
Scapuloperoneal syndromes. Absence of linkage to the 4q35 FSHD locusR Tawil, G J Myers, B Weiffenbach, et al.
Neurology|November 1, 1993
Intranuclear rods in severe congenital nemaline myopathyZ Rifai, A M Kazee, C Kamp, et al.
Pageof 20