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Journal Abstract Search

147 related items for PubMed ID: 14272202

  • 41. Acute renal failure in McArdle's disease.
    Tabata T, Kikunami K, Matsushita Y, Inoue T, Inoue T, Okamoto T, Kono N, Takahashi M, Tarui S, Morii H.
    Nephron; 1986; 44(4):371-4. PubMed ID: 3467218
    [Abstract] [Full Text] [Related]

  • 42. [McArdle's myopathy].
    Drobinskii AD, Stezhka TK.
    Sov Med; 1978 Dec; (12):115-7. PubMed ID: 282676
    [No Abstract] [Full Text] [Related]

  • 43. [Massive rhabdomyolysis revealing a McArdle disease].
    Loupy A, Pouchot J, Hertig A, Bonnard G, Bouvard E, Rondeau E.
    Rev Med Interne; 2007 Jul; 28(7):501-3. PubMed ID: 17383055
    [Abstract] [Full Text] [Related]

  • 44. [A metabolic disease of muscles: the absence of phosphorylase (McArdle-Schmid-Pearson disease)].
    SCHULLER E.
    Presse Med (1893); 1962 Mar 24; 70():715-7. PubMed ID: 13909460
    [No Abstract] [Full Text] [Related]

  • 45. [McArdle's disease--description based on three own observations (author's transl)].
    Berger M, Gibbels E, Leven B, Seiler D.
    Fortschr Neurol Psychiatr Grenzgeb; 1978 Jun 24; 46(6):312-26. PubMed ID: 276513
    [Abstract] [Full Text] [Related]

  • 46. [McArdle's disease: a case report and electrolytes metabolism (author's transl)].
    Uno H, Sumita H, Ogawa A, Kawano K, Kondo K, Ueshima K, Tamada K, Yukawa S, Nomoto H.
    Nihon Naika Gakkai Zasshi; 1979 Jul 10; 68(7):768-75. PubMed ID: 289712
    [No Abstract] [Full Text] [Related]

  • 47. [McArdle's disease (a familial case)].
    Shevchenko AM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1976 Jul 10; 76(5):655-9. PubMed ID: 1065164
    [Abstract] [Full Text] [Related]

  • 48. 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 10; 77(6):1881-7. PubMed ID: 3458722
    [Abstract] [Full Text] [Related]

  • 49. [Hepatic glycogenoses. Correlations between the clinical and biochemical characteristics and the type of enzymatic deficiency: glucose-6-phosphatase, amylo-1-6-glucosidase, phosphorylase].
    GABILAN JC.
    Rev Int Hepatol; 1960 Jun 10; 10():699-818. PubMed ID: 13702771
    [No Abstract] [Full Text] [Related]

  • 50. A female case of glycogen storage myopathy due to phosphorylase kinase deficiency.
    Ohtani Y, Matsuda I, Iwamasa T.
    J Inherit Metab Dis; 1982 Jun 10; 5(2):71-2. PubMed ID: 6820425
    [No Abstract] [Full Text] [Related]

  • 51. Neuropathy in a patient with McArdle's syndrome and diabetes mellitus.
    Davies TJ, Harrop JS, Smith JM, Marks V.
    Horm Metab Res; 1977 Sep 10; 9(5):351-3. PubMed ID: 270456
    [Abstract] [Full Text] [Related]

  • 52. McArdle's disease diagnosed following statin-induced myositis.
    Livingstone C, Al Riyami S, Wilkins P, Ferns GA.
    Ann Clin Biochem; 2004 Jul 10; 41(Pt 4):338-40. PubMed ID: 15298748
    [Abstract] [Full Text] [Related]

  • 53. [Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)].
    Delwaide PJ, Reznik M, Lemaire R, Lelièvre P, Bonnet F.
    Rev Neurol (Paris); 1967 Feb 10; 116(2):119-40. PubMed ID: 5230980
    [No Abstract] [Full Text] [Related]

  • 54. Fatal infantile muscle phosphorylase deficiency.
    Milstein JM, Herron TM, Haas JE.
    J Child Neurol; 1989 Jul 10; 4(3):186-8. PubMed ID: 2768781
    [Abstract] [Full Text] [Related]

  • 55. Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients.
    Roelofs RI, Engel WK, Chauvin PB.
    Science; 1972 Sep 01; 177(4051):795-7. PubMed ID: 4506147
    [Abstract] [Full Text] [Related]

  • 56. McArdle's disease: a review.
    Lubran MM.
    Ann Clin Lab Sci; 1975 Sep 01; 5(2):115-22. PubMed ID: 1092247
    [Abstract] [Full Text] [Related]

  • 57. [McArdle disease revealed by exercise intolerance associated with severe rhabdomyolysis].
    Amezyane T, El Kharras A, Abouzahir A, Fatihi J, Bassou D, Mahassin F, Ghafir D, Ohayon V.
    Ann Endocrinol (Paris); 2009 Dec 01; 70(6):480-4. PubMed ID: 19878922
    [Abstract] [Full Text] [Related]

  • 58. [McArdle's disease: therapeutic use of depot-glucagon].
    Schmid R, Wiethölter H.
    Dtsch Med Wochenschr; 1982 Nov 26; 107(47):1809-11. PubMed ID: 6958445
    [Abstract] [Full Text] [Related]

  • 59. Diagnosis of muscular glycogenosis by in vivo natural abundance 13C NMR spectroscopy.
    Jehenson P, Duboc D, Bloch G, Fardeau M, Syrota A.
    Neuromuscul Disord; 1991 Nov 26; 1(2):99-101. PubMed ID: 1822788
    [Abstract] [Full Text] [Related]

  • 60. Glycogen storage disease type V (Mc Ardle's disease): a report on three cases.
    Krishnamoorthy N, Santosh V, Yasha TC, Mahadevan A, Shankar SK, Jethwani D, Taly AB, Bhanu K, Gayathri N.
    Neurol India; 2011 Nov 26; 59(6):884-6. PubMed ID: 22234204
    [Abstract] [Full Text] [Related]

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