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Journal Abstract Search

133 related items for PubMed ID: 3923581

  • 1. Heterozygote detection in a family of Lapland dogs with a recessively inherited metabolic disease: canine glycogen storage disease type II.
    Walvoort HC, Koster JF, Reuser AJ.
    Res Vet Sci; 1985 Mar; 38(2):174-8. PubMed ID: 3923581
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  • 7. 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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  • 8. The "muscular variant" of Pompe disease: clinical, biochemical and histologic characteristics.
    Temple JK, Dunn DW, Blitzer MG, Shapira E.
    Am J Med Genet; 1985 Jul 17; 21(3):597-604. PubMed ID: 3895931
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  • 9. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
    Didt L, Winkler M, Bührdel P, Bormann M, Böhme HJ, Hofmann E.
    Z Med Lab Diagn; 1988 Jul 17; 29(1):7-11. PubMed ID: 3129881
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  • 11. Type II glycogenosis and thyroxine binding globulin deficiency in the same family.
    Manta P, Kontoleon P, Panousopoulou A, Kalfakis N, Christomanou H, Papapetrou P, Papageorgiou C.
    Funct Neurol; 1996 Jul 17; 11(2-3):105-10. PubMed ID: 8765758
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  • 12. A new diagnostic assay for glycogen storage disease type II in mixed leukocytes.
    Okumiya T, Keulemans JL, Kroos MA, Van der Beek NM, Boer MA, Takeuchi H, Van Diggelen OP, Reuser AJ.
    Mol Genet Metab; 2006 May 17; 88(1):22-8. PubMed ID: 16359900
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  • 13. [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 17; 15(12):705-8. PubMed ID: 342670
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  • 17. [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; 1977 Dec 17; 29(1):46-9. PubMed ID: 10528311
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  • 18. Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.
    Rangdaeng S, Scollard DM, Srichairatanakol S, Sutthachit M, Phornphutkul C.
    J Med Assoc Thai; 1987 Sep 17; 70(9):536-42. PubMed ID: 2960768
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  • 19. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T, Sandig KR.
    Kinderarztl Prax; 1984 Aug 17; 52(8):377-82. PubMed ID: 6384623
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  • 20. Genotyping glycogen storage disease type II and type V in cattle reared in the Czech Republic.
    Cítek J, Rehout V, Vecerek L, Hájková J.
    J Vet Med A Physiol Pathol Clin Med; 2007 Jun 17; 54(5):257-9. PubMed ID: 17523960
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