These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 986033)

  • 21. Myoglobinuria and skeletal muscle phosphorylase deficiency: report of a case of McArdle's disease.
    Nixon JC; Hobbs WK; Greenblatt J
    Can Med Assoc J; 1966 May; 94(19):977-85. PubMed ID: 4952390
    [TBL] [Abstract][Full Text] [Related]  

  • 22. McArdle's disease--what limit to the age of onset?
    Hewlett RH; Gardner-Thorpe C
    S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990
    [TBL] [Abstract][Full Text] [Related]  

  • 23. McArdle's disease: biochemical and molecular genetic studies.
    Servidei S; Shanske S; Zeviani M; Lebo R; Fletterick R; DiMauro S
    Ann Neurol; 1988 Dec; 24(6):774-81. PubMed ID: 3207360
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Myophosphorylase deficiency and limb-girdle muscular dystrophy in the same pedigree.
    Nishio T; Sunohara N; Nonaka I; Tsujino S; Sugie H
    Acta Neurol Scand; 1998 Nov; 98(5):364-7. PubMed ID: 9858109
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ischemic exercise test: failure to detect partial expression of McArdle's disease.
    Taylor RG; Lieberman JS; Portwood MM
    Muscle Nerve; 1987; 10(6):546-51. PubMed ID: 3476851
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review].
    Mattle H; Jerusalem F
    Schweiz Med Wochenschr; 1977 Apr; 107(13):428-36. PubMed ID: 139680
    [TBL] [Abstract][Full Text] [Related]  

  • 28. McArdle's disease heterozygotes. Metabolic adaptation assessed using 31P-nuclear magnetic resonance.
    Bogusky RT; Taylor RG; Anderson LJ; Angelos KL; Lieberman JS; Walsh DA
    J Clin Invest; 1986 Jun; 77(6):1881-7. PubMed ID: 3458722
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [A metabolic disease of muscles: the absence of phosphorylase (McArdle-Schmid-Pearson disease)].
    SCHULLER E
    Presse Med (1893); 1962 Mar; 70():715-7. PubMed ID: 13909460
    [No Abstract]   [Full Text] [Related]  

  • 30. Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci.
    Tsujino S; Shanske S; Carroll JE; Sabina RL; DiMauro S
    Neuromuscul Disord; 1995 Jul; 5(4):263-6. PubMed ID: 7580237
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P; Nolte J; Meisel D; Dichgans J; Jerusalem F
    Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():1277-80. PubMed ID: 274025
    [No Abstract]   [Full Text] [Related]  

  • 32. Metabolism of branched-chain amino acids and ammonia during exercise: clues from McArdle's disease.
    Wagenmakers AJ; Coakley JH; Edwards RH
    Int J Sports Med; 1990 May; 11 Suppl 2():S101-13. PubMed ID: 2193889
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
    Coll Cantí J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ
    Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989
    [No Abstract]   [Full Text] [Related]  

  • 34. Myophosphorylase deficiency associated with a defect in complex I of the mitochondrial respiratory chain.
    Rubio JC; Martín MA; Bautista J; Campos Y; Segura D; Cabello A; Chinchón I; Arenas J
    J Neurol Sci; 1998 Dec; 161(2):110-3. PubMed ID: 9879690
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A metabolic myopathy due to absence of muscle phosphorylase.
    PEARSON CM; RIMER DG; MOMMAERTS WF
    Am J Med; 1961 Apr; 30():502-17. PubMed ID: 13733779
    [No Abstract]   [Full Text] [Related]  

  • 36. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
    Baqué S; Newgard CB; Gerard RD; Guinovart JJ; Gómez-Foix AM
    Biochem J; 1994 Dec; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro.
    Pari G; Crerar MM; Nalbantoglu J; Shoubridge E; Jani A; Tsujino S; Shanske S; DiMauro S; Howell JM; Karpati G
    Neurology; 1999 Oct; 53(6):1352-4. PubMed ID: 10522901
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Phosphorylase a in human skeletal muscle during exercise and electrical stimulation.
    Gollnick PD; Karlsson J; Piehl K; Saltin B
    J Appl Physiol Respir Environ Exerc Physiol; 1978 Dec; 45(6):852-7. PubMed ID: 730587
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [McArdle's syndrome (myopathy in muscle phosphorylase deficiency)].
    Schimrigk K; Mertens HG; Ricker K; Führ J; Eyer P; Pette D
    Klin Wochenschr; 1967 Jan; 45(1):1-17. PubMed ID: 6031735
    [No Abstract]   [Full Text] [Related]  

  • 40. [Changes in glycogen metabolism in hereditary muscular diseases (review)].
    Rozenfel'd EL
    Vopr Med Khim; 1986; 32(4):12-20. PubMed ID: 2945316
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.