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.


PUBMED FOR HANDHELDS

Journal Abstract Search


77 related items for PubMed ID: 5229456

  • 1. McArdle's disease: three cases in an Australian family.
    Hammett JF, Bale P, Basser LS, Neale FC.
    Proc Aust Assoc Neurol; 1966; 4():21-5. PubMed ID: 5229456
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. The clinical diagnosis of McArdle's disease. Identification of another family with deficiency of muscle phosphorylase.
    Rowland LP, Lovelace RE, Schotland DL, Araki S, Carmel P.
    Neurology; 1966 Jan; 16(1):93-100. PubMed ID: 5215287
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. McArdle's disease and anaesthesia: case reports. Review of potential problems and association with malignant hyperthermia.
    Bollig G, Mohr S, Raeder J.
    Acta Anaesthesiol Scand; 2005 Sep; 49(8):1077-83. PubMed ID: 16095447
    [Abstract] [Full Text] [Related]

  • 9. Histopathology of McArdle's disease in a family.
    Bale P, Hammett JF, Neale FC.
    J Pathol Bacteriol; 1967 Oct; 94(2):293-300. PubMed ID: 6066477
    [No Abstract] [Full Text] [Related]

  • 10. [Nation-wide survey on muscle glycogen storage disease (MGSDs) and comparison with our experiences in diagnosis of MGSDs].
    Fukuda T, Sugie H, Ito M, Sugie Y, Saito K, Nishino I, Shimizu T.
    Rinsho Shinkeigaku; 2003 May; 43(5):243-8. PubMed ID: 12931628
    [Abstract] [Full Text] [Related]

  • 11. [Myopathy--with reference to hereditary myopathy].
    Araki S.
    Saishin Igaku; 1966 Apr; 21(4):732-45. PubMed ID: 5340851
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene.
    Paradas C, Fernandez-Cadenas I, Gallardo E, Lligé D, Arenas J, Illa I, Andreu AL.
    Neurosci Lett; 2005 Dec 31; 391(1-2):28-31. PubMed ID: 16154688
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. McArdle's disease: lack of muscle phosphorylase.
    Dawson DM, Spong FL, Harrington JF.
    Ann Intern Med; 1968 Aug 31; 69(2):229-35. PubMed ID: 5243846
    [No Abstract] [Full Text] [Related]

  • 19. [McArdle's syndrome].
    Lobzin VS, Zagorodnyĭ RI, Glushkov BS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Aug 31; 73(6):820-5. PubMed ID: 4518645
    [No Abstract] [Full Text] [Related]

  • 20. Acute renal failure in McArdle's disease and myoglobinuric states.
    Paster SB, Adams DF, Hollenberg NK.
    Radiology; 1975 Mar 31; 114(3):567-70. PubMed ID: 1054521
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 4.