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Related Articles by Review for PubMed (Select 18401027)

1.

Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?

Ørngreen MC, Schelhaas HJ, Jeppesen TD, Akman HO, Wevers RA, Andersen ST, ter Laak HJ, van Diggelen OP, DiMauro S, Vissing J.

Neurology. 2008 May 13;70(20):1876-82. doi: 10.1212/01.wnl.0000289190.66955.67. Epub 2008 Apr 9.

PMID:
18401027
2.

Adult phosphorylase b kinase deficiency.

Clemens PR, Yamamoto M, Engel AG.

Ann Neurol. 1990 Oct;28(4):529-38. Review.

PMID:
2252364
3.

A case of McArdle disease: efficacy of vitamin B6 on fatigability and impaired glycogenolysis.

Izumi R, Suzuki N, Kato K, Warita H, Tateyama M, Nakashima I, Itoyama Y.

Intern Med. 2010;49(15):1623-5. Epub 2010 Aug 2. Review.

4.

[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].

Laforêt P, Eymard B, Lombès A, Duboc D, Jehenson P, Rocchiccioli F, Chaussain M, Chateau D, Brunet P, Fardeau M.

Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Review. French.

PMID:
8944243
5.

Lactate production and clearance in exercise. Effects of training. A mini-review.

Stallknecht B, Vissing J, Galbo H.

Scand J Med Sci Sports. 1998 Jun;8(3):127-31. Review.

PMID:
9659671
6.

Phosphorylase b kinase deficiency in man: a review.

Van den Berg IE, Berger R.

J Inherit Metab Dis. 1990;13(4):442-51. Review.

PMID:
2122111
7.

McArdle disease: molecular genetic update.

Andreu AL, Nogales-Gadea G, Cassandrini D, Arenas J, Bruno C.

Acta Myol. 2007 Jul;26(1):53-7. Review.

8.

[Metabolic myopathies--part I: disorders of the carbohydrate metabolism].

Finsterer J.

Fortschr Neurol Psychiatr. 2011 Oct;79(10):598-605; quiz 606. doi: 10.1055/s-0031-1281721. Epub 2011 Oct 11. Review. German. No abstract available.

PMID:
21989512
9.

The pathophysiology of McArdle's disease: clues to regulation in exercise and fatigue.

Lewis SF, Haller RG.

J Appl Physiol (1985). 1986 Aug;61(2):391-401. Review.

PMID:
3528113
10.

McArdle's disease presenting with asymmetric, late-onset arm weakness.

Wolfe GI, Baker NS, Haller RG, Burns DK, Barohn RJ.

Muscle Nerve. 2000 Apr;23(4):641-5. Review.

PMID:
10716777
11.

Genetic deficiencies of the glycogen phosphorylase system.

Hendrickx J, Willems PJ.

Hum Genet. 1996 May;97(5):551-6. Review.

PMID:
8655128
12.

Glycogen Storage Disease Type V.

Martín MA, Lucía A, Arenas J, Andreu AL.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2006 Apr 19 [updated 2014 Jun 26].

13.

Skeletal muscle disorders and associated factors that limit exercise performance.

Lewis SF, Haller RG.

Exerc Sport Sci Rev. 1989;17:67-113. Review.

PMID:
2676557
14.

[Metabolic intolerance to exercise].

Arenas J, Martín MA.

Neurologia. 2003 Jul-Aug;18(6):291-302. Review. Spanish.

PMID:
12838448
15.

Glycogen turnover forms lactate during exercise.

Shulman RG.

Exerc Sport Sci Rev. 2005 Oct;33(4):157-62. Review.

PMID:
16239831
16.

McArdle disease: what do neurologists need to know?

Lucia A, Nogales-Gadea G, Pérez M, Martín MA, Andreu AL, Arenas J.

Nat Clin Pract Neurol. 2008 Oct;4(10):568-77. doi: 10.1038/ncpneuro0913. Review.

PMID:
18833216
17.

McArdle's disease-muscle glycogen phosphorylase deficiency.

Bartram C, Edwards RH, Beynon RJ.

Biochim Biophys Acta. 1995 Aug 15;1272(1):1-13. Review. No abstract available.

PMID:
7662715
18.

Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.

Shin YS.

Semin Pediatr Neurol. 2006 Jun;13(2):115-20. Review.

PMID:
17027861
19.

[Glycogen storage disease type VIII].

Nishigaki T.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):56-9. Review. Japanese. No abstract available.

PMID:
9589988
20.

Myophosphorylase deficiency (glycogenosis type V; McArdle disease).

Dimaur S, Andreu AL, Bruno C, Hadjigeorgiou GM.

Curr Mol Med. 2002 Mar;2(2):189-96. Review.

PMID:
11949935
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