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3. Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease. Ninomiya N; Matsuda I; Fukuda S; Iwamasa T; Osame M Histochem J; 1983 Jun; 15(6):601-4. PubMed ID: 6347982 [No Abstract] [Full Text] [Related]
4. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods. Ninomiya N; Iwamasa T; Matsuda I; Nonaka I J Inherit Metab Dis; 1983; 6(3):131-2. PubMed ID: 6422147 [No Abstract] [Full Text] [Related]
5. [Late infantile form of Pompe's disease. Deficiency of alpha-1,4-glucosidase (acid maltase)]. Colomer J; Roig M; Campistol J; Rullan G; Fernández-Alvarez E An Esp Pediatr; 1984 Sep; 21(3):250-9. PubMed ID: 6391315 [TBL] [Abstract][Full Text] [Related]
12. Subcellular distribution of acid alpha-glucosidase in fibroblasts and of antigenically cross-reactive material in Pompe's disease fibroblasts. Iwamasa T; Nashiro K; Ohshita T; Matsuda I Histochem J; 1986; 18(11-12):613-24. PubMed ID: 3549635 [TBL] [Abstract][Full Text] [Related]
13. First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid alpha-glucosidase in chorionic villous biopsy using antibodies. Grubisic A; Shin YS; Meyer W; Endres W; Becker U; Wischerath H Clin Genet; 1986 Oct; 30(4):298-301. PubMed ID: 3098466 [TBL] [Abstract][Full Text] [Related]
14. 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; 70(9):536-42. PubMed ID: 2960768 [No Abstract] [Full Text] [Related]
15. [Cardiomuscular lysosomal glycogenosis in adults without known enzyme deficiency. A cause of familial myocardiopathy and lysosomal glycogen overload with normal acid maltase]. Bru P; Pellissier JF; Gatau-Pelanchon J; Faugère G; de Barsy T; Levy S; Gérard R Arch Mal Coeur Vaiss; 1988 Jan; 81(1):109-14. PubMed ID: 3130016 [TBL] [Abstract][Full Text] [Related]
16. 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; 45(1):51-61. PubMed ID: 6199887 [TBL] [Abstract][Full Text] [Related]
17. 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; 29(1):7-11. PubMed ID: 3129881 [No Abstract] [Full Text] [Related]
18. Angiocardiographic and enzyme studies in a patient with type II glycogenosis (Pompe's disease). A case report. Bonnici F; Shapiro R; Joffe HS; Petersen EM S Afr Med J; 1980 Nov; 58(21):860-2. PubMed ID: 6777881 [TBL] [Abstract][Full Text] [Related]
19. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle. Van der Ploeg AT; Loonen MC; Bolhuis PA; Busch HM; Reuser AJ; Galjaard H Pediatr Res; 1988 Jul; 24(1):90-4. PubMed ID: 2970619 [TBL] [Abstract][Full Text] [Related]
20. Diagnosis of Pompe's disease using pyridylamino-maltooligosaccharides as substrates of alpha-1,4-glucosidase. Midorikawa M; Okada S; Kato T; Yutaka T; Yabuuchi H Clin Chim Acta; 1985 Apr; 147(2):97-102. PubMed ID: 3886206 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]