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Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.

Publication ,  Journal Article
Gospe, SM; El-Schahawi, M; Shanske, S; Bruno, C; DiMauro, S; Hoye, E; Walsh, DA; Gorin, FA
Published in: Neurology
October 1998
Published version (DOI) Link to item

Duke Scholars

Sidney M. Gospe Jr.
Author Sidney M. Gospe Jr. Pediatrics, Neurology

Published In

Neurology

DOI

10.1212/wnl.51.4.1228

ISSN

0028-3878

Publication Date

October 1998

Volume

51

Issue

4

Start / End Page

1228 / 1229

Location

United States

Related Subject Headings

  • Polymorphism, Restriction Fragment Length
  • Phosphorylases
  • Neurology & Neurosurgery
  • Mutation
  • Muscle, Skeletal
  • Humans
  • Glycogen Storage Disease Type V
  • Female
  • Creatine Kinase
  • Adolescent
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Gospe, S. M., El-Schahawi, M., Shanske, S., Bruno, C., DiMauro, S., Hoye, E., … Gorin, F. A. (1998). Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. Neurology, 51(4), 1228–1229. https://doi.org/10.1212/wnl.51.4.1228
Gospe, S. M., M. El-Schahawi, S. Shanske, C. Bruno, S. DiMauro, E. Hoye, D. A. Walsh, and F. A. Gorin. “Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.” Neurology 51, no. 4 (October 1998): 1228–29. https://doi.org/10.1212/wnl.51.4.1228.
Gospe SM, El-Schahawi M, Shanske S, Bruno C, DiMauro S, Hoye E, et al. Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. Neurology. 1998 Oct;51(4):1228–9.
Gospe, S. M., et al. “Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.” Neurology, vol. 51, no. 4, Oct. 1998, pp. 1228–29. Pubmed, doi:10.1212/wnl.51.4.1228.
Gospe SM, El-Schahawi M, Shanske S, Bruno C, DiMauro S, Hoye E, Walsh DA, Gorin FA. Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase. Neurology. 1998 Oct;51(4):1228–1229.

Published In

Neurology

DOI

10.1212/wnl.51.4.1228

ISSN

0028-3878

Publication Date

October 1998

Volume

51

Issue

4

Start / End Page

1228 / 1229

Location

United States

Related Subject Headings

  • Polymorphism, Restriction Fragment Length
  • Phosphorylases
  • Neurology & Neurosurgery
  • Mutation
  • Muscle, Skeletal
  • Humans
  • Glycogen Storage Disease Type V
  • Female
  • Creatine Kinase
  • Adolescent