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42. Hereditary absence of muscle phosphorylase (McArdle's syndrome). SCHMID R; HAMMAKER L N Engl J Med; 1961 Feb; 264():223-5. PubMed ID: 13747935 [No Abstract] [Full Text] [Related]
43. Myopathy in McArdle's syndrome. Improvement with a high-protein diet. Slonim AE; Goans PJ N Engl J Med; 1985 Feb; 312(6):355-9. PubMed ID: 3855499 [No Abstract] [Full Text] [Related]
44. Genetic analysis of Japanese patients with myophosphorylase deficiency (McArdle's disease): single-codon deletion in exon 17 is the predominant mutation. Sugie H; Sugie Y; Ito M; Fukuda T; Nonaka I; Igarashi Y Clin Chim Acta; 1995 Apr; 236(1):81-6. PubMed ID: 7664468 [TBL] [Abstract][Full Text] [Related]
45. Molecular characterization of McArdle's disease in two large Finnish families. Bruno C; Löfberg M; Tamburino L; Jänkälä H; Hadjigeorgiou GM; Andreu AL; Shanske S; Somer H; DiMauro S J Neurol Sci; 1999 Jun; 165(2):121-5. PubMed ID: 10450796 [TBL] [Abstract][Full Text] [Related]
46. Selective atrophy of type 1 muscle fibers in McArdle's disease. Felice KJ; Grunnet ML; Sima AA Neurology; 1996 Aug; 47(2):581-3. PubMed ID: 8757045 [TBL] [Abstract][Full Text] [Related]
47. MCARDLE'S DISEASE PRESENTING AS CONVULSION AND RHABDOMYOLYSIS. SALMON SE; TURNER CE Am J Med; 1965 Jul; 39():142-6. PubMed ID: 14314229 [No Abstract] [Full Text] [Related]
48. Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease). Tsujino S; Shanske S; DiMauro S N Engl J Med; 1993 Jul; 329(4):241-5. PubMed ID: 8316268 [TBL] [Abstract][Full Text] [Related]
49. Myopathy in McArdle's syndrome. Thompson PD; Flynn MM N Engl J Med; 1985 Jun; 312(23):1518-9. PubMed ID: 3857462 [No Abstract] [Full Text] [Related]
50. A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease. Bruno C; Tamburino L; Kawashima N; Andreu AL; Shanske S; Hadjigeorgiou GM; Kawashima A; DiMauro S Neuromuscul Disord; 1999 Jan; 9(1):34-7. PubMed ID: 10063833 [TBL] [Abstract][Full Text] [Related]
51. An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease). Tsujino S; Rubin LA; Shanske S; DiMauro S Hum Mutat; 1994; 4(1):73-5. PubMed ID: 7951262 [No Abstract] [Full Text] [Related]
53. 2,4-Dinitrophenol, muscle biopsy, and McArdle's disease. Heller SL; Brooke MH; Kaiser KK; Choski R Neurology; 1988 Jan; 38(1):15-9. PubMed ID: 3422109 [TBL] [Abstract][Full Text] [Related]
54. In McArdle disease, phosphorylase deficiency is the tip of an iceberg. Willner JH; Cerri CG; Wood DS; Ponzetto-Zimmerman C; Reydel PM Trans Am Neurol Assoc; 1981; 106():208-9. PubMed ID: 6294950 [No Abstract] [Full Text] [Related]
55. McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote. Schmidt B; Servidei S; Gabbai AA; Silva AC; de Sousa Bulle de Oliveira A; DiMauro S Neurology; 1987 Sep; 37(9):1558-61. PubMed ID: 3476861 [TBL] [Abstract][Full Text] [Related]
56. [Muscular intolerance of exercise. Current data]. Serratrice G Presse Med; 1998 Oct; 27(33):1683-6. PubMed ID: 9834785 [TBL] [Abstract][Full Text] [Related]
57. McArdle's disease with non-insulin-dependent diabetes mellitus: the beneficial effects of hyperglycemia and hyperinsulinemia for exercise intolerance. Yamauchi A; Amano K; Ichikawa Y; Nakamoto S; Takei I; Maruyama H; Kono N; Saruta T Intern Med; 1996 May; 35(5):403-6. PubMed ID: 8797056 [TBL] [Abstract][Full Text] [Related]
58. McArdle's disease: a review. Lubran MM Ann Clin Lab Sci; 1975; 5(2):115-22. PubMed ID: 1092247 [TBL] [Abstract][Full Text] [Related]
59. [McArdle's disease in adults: clinical and genetic study]. Olmos JM; Zarrabeitia MT; Valero MC; Figols J; Matorras P; Riancho JA Med Clin (Barc); 1997 Nov; 109(19):753-5. PubMed ID: 9470186 [TBL] [Abstract][Full Text] [Related]