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Journal Abstract Search

278 related items for PubMed ID: 6791275

  • 21. [Myopathy caused by acid maltase deficiency in an adult].
    Cartier L, Cea JG, Slachevsky A.
    Rev Med Chil; 1995 Jun; 123(6):758-61. PubMed ID: 8525231
    [Abstract] [Full Text] [Related]

  • 22. Biopsy-proven alpha-glucosidase deficiency with normal lymphocyte enzyme activity.
    Whitaker CH, Felice KJ, Natowicz M.
    Muscle Nerve; 2004 Mar; 29(3):440-2. PubMed ID: 14981745
    [Abstract] [Full Text] [Related]

  • 23. Acid maltase deficiency in childhood. Early diagnosis and clinical follow-up of late-onset glycogen storage disease type II.
    di Fiore MT, Manfredi R, Marri L, Zucchini A, Azzaroli L, Manfredi G.
    Acta Neurol (Napoli); 1993 Aug; 15(4):258-67. PubMed ID: 8249669
    [Abstract] [Full Text] [Related]

  • 24. Acid maltase deficiency in adults. Clinical, morphological and biochemical study of three patients.
    Bertagnolio B, Di Donato S, Peluchetti D, Rimoldi M, Storchi G, Cornelio F.
    Eur Neurol; 1978 Aug; 17(4):193-204. PubMed ID: 357152
    [Abstract] [Full Text] [Related]

  • 25. Infantile acid maltase deficiency. III. Ultrastructure of metachromatic material and glycogen in muscle fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Aug; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 26. Glycogen storage disease: clinical, biochemical, and molecular heterogeneity.
    Shin YS.
    Semin Pediatr Neurol; 2006 Jun; 13(2):115-20. PubMed ID: 17027861
    [Abstract] [Full Text] [Related]

  • 27. Lysosomal glycogen storage disease without acid maltase deficiency.
    Riggs JE, Schochet SS, Gutmann L, Shanske S, Neal WA, DiMauro S.
    Neurology; 1983 Jul; 33(7):873-7. PubMed ID: 6408499
    [Abstract] [Full Text] [Related]

  • 28. alpha-Glucosidase isoenzymes in normal and acid maltase-deficient human skeletal muscles.
    Usuki F, Ishiura S, Nonaka I, Sugita H.
    Muscle Nerve; 1988 Apr; 11(4):365-71. PubMed ID: 3135493
    [Abstract] [Full Text] [Related]

  • 29. [Severe form of juvenile type II glycogenosis in a compound-heterozygous boy (Tyr-292--> Cys/Arg-854-->Stop)].
    Castro-Gago M, Eirís-Puñal J, Rodríguez-Núñez A, Pintos-Martínez E, Benlloch-Marín T, Barros-Angueira F.
    Rev Neurol; 1988 Apr; 29(1):46-9. PubMed ID: 10528311
    [Abstract] [Full Text] [Related]

  • 30. Pompe disease (glycogen storage disease type II): clinical features and enzyme replacement therapy.
    van der Beek NA, Hagemans ML, van der Ploeg AT, Reuser AJ, van Doorn PA.
    Acta Neurol Belg; 2006 Jun; 106(2):82-6. PubMed ID: 16898258
    [Abstract] [Full Text] [Related]

  • 31. Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in in cultured muscle.
    Askanas V, Engel WK, DiMauro S, Brooks BR, Mehler M.
    N Engl J Med; 1976 Mar 11; 294(11):573-8. PubMed ID: 1060914
    [Abstract] [Full Text] [Related]

  • 32. Adult-onset acid maltase deficiency: a postmortem study.
    DiMauro S, Stern LZ, Mehler M, Nagle RB, Payne C.
    Muscle Nerve; 1978 Mar 11; 1(1):27-36. PubMed ID: 377069
    [Abstract] [Full Text] [Related]

  • 33. Lysosomal glycogen storage disease without deficiency of acid alpha-glucosidase.
    Ullrich K, von Bassewitz D, Shin J, Korinthenberg R, Sewell S, von Figura K.
    Prog Clin Biol Res; 1989 Mar 11; 306():163-71. PubMed ID: 2500669
    [No Abstract] [Full Text] [Related]

  • 34. Acid maltase deficiency in adolescence: report of an unusual case.
    Olguntürk R, Bilgiç A, Cağlar M, Sinangil F.
    Turk J Pediatr; 1982 Mar 11; 24(2):115-9. PubMed ID: 6214067
    [No Abstract] [Full Text] [Related]

  • 35. Glycogen storage myopathy with abnormal lactate dehydrogenase.
    Nagata N, Miike T, Matsuda I, Shikama H, Tokumitsu Y, Ui M.
    Neuropediatrics; 1982 May 11; 13(2):103-7. PubMed ID: 6957732
    [Abstract] [Full Text] [Related]

  • 36. Acid maltase deficiency in adults. A study of five cases.
    Lenders MB, Martin JJ, de Barsy T, Ceuterick C, Marchau M.
    Acta Neurol Belg; 1986 May 11; 86(3):152-60. PubMed ID: 3090848
    [Abstract] [Full Text] [Related]

  • 37. [A retrospective study of six patients with late-onset Pompe disease].
    Saux A, Laforet P, Pagès AM, Figarella-Branger D, Pellissier JF, Pagès M, Labauge P.
    Rev Neurol (Paris); 2008 Apr 11; 164(4):336-42. PubMed ID: 18439925
    [Abstract] [Full Text] [Related]

  • 38.
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  • 39. Adult-onset acid maltase deficiency in siblings.
    Miyamoto Y, Etoh Y, Joh R, Noda K, Ohya I, Morimatsu M.
    Acta Pathol Jpn; 1985 Nov 11; 35(6):1533-42. PubMed ID: 3937437
    [Abstract] [Full Text] [Related]

  • 40. Multiple muscles in the AMD quail can be "cross-corrected" of pathologic glycogen accumulation after intravenous injection of an [E1-, polymerase-] adenovirus vector encoding human acid-alpha-glucosidase.
    McVie-Wylie AJ, Ding EY, Lawson T, Serra D, Migone FK, Pressley D, Mizutani M, Kikuchi T, Chen YT, Amalfitano A.
    J Gene Med; 2003 May 11; 5(5):399-406. PubMed ID: 12731088
    [Abstract] [Full Text] [Related]

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