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Journal Abstract Search

168 related items for PubMed ID: 6368168

  • 21. [Clinical follow-up in the adult (myopathic) form of glycogenosis type II].
    Schejbal P, Kutzner M, Delank HW, Gullotta F.
    Schweiz Arch Neurol Psychiatr (1985); 1986; 137(3):39-47. PubMed ID: 2425422
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  • 22. Juvenile onset acid maltase deficiency presenting as a rigid spine syndrome.
    Kostera-Pruszczyk A, Opuchlik A, Lugowska A, Nadaj A, Bojakowski J, Tylki-Szymanska A, Kaminska A.
    Neuromuscul Disord; 2006 Apr; 16(4):282-5. PubMed ID: 16531044
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  • 24. [Hepatic involvement in a case of lysosomal glycogen storage disease with normal acid maltase].
    Matsumoto S, Yamada T, Tanaka K, Hara H, Nonaka I, Uchida T, Miyagi Y, Fukutomi T, Kira J.
    Rinsho Shinkeigaku; 1999 Jul; 39(7):717-21. PubMed ID: 10548908
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  • 25. Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency).
    Loonen MC, Schram AW, Koster JF, Niermeijer MF, Busch HF, Martin JJ, Brouwer-Kelder B, Mekes W, Slee RG, Tager JM.
    Clin Genet; 1981 Jan; 19(1):55-63. PubMed ID: 7006871
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  • 26. The pathology of type II skeletal muscle glycogenosis. A light and electron-microscopic study.
    Hudgson P, Fulthorpe JJ.
    J Pathol; 1975 Jul; 116(3):139-47. PubMed ID: 172619
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  • 27. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H, Goebel HH, Stefan H, Seidel D, Kohlschütter A.
    J Clin Chem Clin Biochem; 1977 Dec; 15(12):705-8. PubMed ID: 342670
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  • 29. Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patients.
    Matsuishi T, Yoshino M, Terasawa K, Nonaka I.
    Arch Neurol; 1984 Jan; 41(1):47-52. PubMed ID: 6360103
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  • 30. [Acid maltase deficiency in 2 adolescent siblings].
    Gracia P, Benlloch T, de la Fuente G, Durántez A, Espanña P, Cánovas A, Illera ER.
    Med Clin (Barc); 1982 Sep 16; 79(5):227-31. PubMed ID: 6755088
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  • 31. Apparent normal leukocyte acid maltase activity in glycogen storage disease type II (Pompe's disease).
    Potter JL, Robinson HB, Kramer JD, Schafter IA.
    Clin Chem; 1980 Dec 16; 26(13):1914-5. PubMed ID: 7002367
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  • 32. [Myopathy in the adult form of glycogenosis II. Two case reports and review of the literature].
    Horstmann S, Meier C, Mumenthaler M, Gitzelmann R.
    Fortschr Neurol Psychiatr; 1990 Sep 16; 58(9):343-50. PubMed ID: 2175729
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  • 33. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A, Massin M, Lombet J, Grattagliano B, Soyeur D, Rigo J, Koulischer L, Van Hoof F.
    Am J Med Genet; 1997 Oct 17; 72(2):135-42. PubMed ID: 9382133
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  • 34. Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy.
    Winkel LP, Kamphoven JH, van den Hout HJ, Severijnen LA, van Doorn PA, Reuser AJ, van der Ploeg AT.
    Muscle Nerve; 2003 Jun 17; 27(6):743-51. PubMed ID: 12766987
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  • 35. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM.
    Ann Clin Lab Sci; 1982 Jun 17; 12(6):431-8. PubMed ID: 6817693
    [Abstract] [Full Text] [Related]

  • 36. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982 Jun 17; 98(9):709-16. PubMed ID: 7049663
    [No Abstract] [Full Text] [Related]

  • 37. [A case of adult-onset nemaline myopathy (adult-onset rod disease) with distal muscular hypertrophy].
    Mitsui T, Miyata K, Kira J, Kobayashi T, Goto I.
    Rinsho Shinkeigaku; 1991 May 17; 31(5):546-9. PubMed ID: 1657478
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  • 40. [Pulmonary hypertension due to glycogen storage disease type II (Pompe's disease): a case report].
    Inoue S, Nakamura T, Hasegawa K, Tadaoka S, Samukawa M, Nezuo S, Sawayama T, Higashi Y, Shirabe T.
    J Cardiol; 1989 Mar 17; 19(1):323-32. PubMed ID: 2810049
    [Abstract] [Full Text] [Related]

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