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Journal Abstract Search

147 related items for PubMed ID: 14272202

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. McArdle's disease in the 1980s.
    Layzer RB.
    N Engl J Med; 1985 Feb 07; 312(6):370-1. PubMed ID: 3855500
    [No Abstract] [Full Text] [Related]

  • 23. Glycogen storage disease in skeletal muscle. Morphological, ultrastructural and biochemical aspects in 10 cases.
    Cabello A, Benlloch T, Franch O, Feliú JF, Ricoy JR.
    Acta Neuropathol Suppl; 1981 Feb 07; 7():297-300. PubMed ID: 6939256
    [Abstract] [Full Text] [Related]

  • 24. A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE.
    TOBIN RB, COLEMAN WA.
    Ann Intern Med; 1965 Feb 07; 62():313-27. PubMed ID: 14259214
    [No Abstract] [Full Text] [Related]

  • 25. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
    Daegelen-Proux D, Kahn A, Marie J, Dreyfus JC.
    Ann Hum Genet; 1981 May 07; 45(2):113-20. PubMed ID: 6797345
    [Abstract] [Full Text] [Related]

  • 26. MCARDLE'S DISEASE PRESENTING AS CONVULSION AND RHABDOMYOLYSIS.
    SALMON SE, TURNER CE.
    Am J Med; 1965 Jul 07; 39():142-6. PubMed ID: 14314229
    [No Abstract] [Full Text] [Related]

  • 27. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
    Daegelen D, Munnich A, Levin MJ, Girault A, Goasguen J, Kahn A, Dreyfus JC.
    Ann Hum Genet; 1983 May 07; 47(2):107-15. PubMed ID: 6576726
    [Abstract] [Full Text] [Related]

  • 28. Selective atrophy of type 1 muscle fibers in McArdle's disease.
    Felice KJ, Grunnet ML, Sima AA.
    Neurology; 1996 Aug 07; 47(2):581-3. PubMed ID: 8757045
    [Abstract] [Full Text] [Related]

  • 29. How sweet it is: McArdle's disease case report and discussion.
    Coates RA.
    J Insur Med; 2009 Aug 07; 41(2):136-41. PubMed ID: 19845217
    [No Abstract] [Full Text] [Related]

  • 30. 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 07; 94(19):977-85. PubMed ID: 4952390
    [Abstract] [Full Text] [Related]

  • 31. Ultrastructural studies of muscle in McArdle's disease.
    Schotland DL, Spiro D, Rowland LP, Carmel P.
    J Neuropathol Exp Neurol; 1965 Oct 07; 24(4):629-44. PubMed ID: 5213729
    [No Abstract] [Full Text] [Related]

  • 32. Two novel mutations in the muscle glycogen phosphorylase gene in McArdle's disease.
    Gámez J, Rubio JC, Martín MA, Fernández-Cadenas I, Garcia-Arumi E, Andreu AL, Arenas J.
    Muscle Nerve; 2003 Sep 07; 28(3):380-2. PubMed ID: 12929201
    [Abstract] [Full Text] [Related]

  • 33. McArdle's syndrome. Fine structural changes in muscle.
    Korényi-Both A, Smith BH, Baruah JK.
    Acta Neuropathol; 1977 Sep 26; 40(1):11-9. PubMed ID: 269622
    [Abstract] [Full Text] [Related]

  • 34. [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 29; 109(19):753-5. PubMed ID: 9470186
    [Abstract] [Full Text] [Related]

  • 35. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P, Nolte J, Meisel D, Dichgans J, Jerusalem F.
    Verh Dtsch Ges Inn Med; 1997 Nov 29; 83():1277-80. PubMed ID: 274025
    [No Abstract] [Full Text] [Related]

  • 36. Molecular and clinical study of McArdle's disease in a cohort of 123 European patients. Identification of 20 novel mutations.
    Vieitez I, Teijeira S, Fernandez JM, San Millan B, Miranda S, Ortolano S, Louis S, Laforet P, Navarro C.
    Neuromuscul Disord; 2011 Dec 29; 21(12):817-23. PubMed ID: 21802952
    [Abstract] [Full Text] [Related]

  • 37. Glycogenosis 5 or McArdle's disease: case for diagnosis.
    Mil Med; 1983 Jan 29; 148(1):64, 69, 73. PubMed ID: 6402732
    [No Abstract] [Full Text] [Related]

  • 38. Early electromyographic findings in asymptomatic siblings with McArdle's disease.
    Suzuki S, Sato H, Nogawa S, Tanaka K, Amano T, Fukuuchi Y.
    Eur Neurol; 2002 Jan 29; 47(4):245-6. PubMed ID: 12037441
    [No Abstract] [Full Text] [Related]

  • 39. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.
    Sato K, Imai F, Hatayama I, Roelofs RI.
    Biochem Biophys Res Commun; 1977 Sep 23; 78(2):663-8. PubMed ID: 269730
    [No Abstract] [Full Text] [Related]

  • 40. [Scintigraphic demonstration of a iatrogenic rhabdomyolysis in McArdle's syndrome (author's transl)].
    Neumann P, Rumpf KW, Kaiser H, Meinck HM, Goebel HH, Schicha H, Emrich D.
    Nuklearmedizin; 1982 Feb 23; 21(1):12-5. PubMed ID: 6210883
    [No Abstract] [Full Text] [Related]

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