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3. [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; 164(4):336-42. PubMed ID: 18439925 [TBL] [Abstract][Full Text] [Related]
4. [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; 79(5):227-31. PubMed ID: 6755088 [No Abstract] [Full Text] [Related]
5. [EMG-findings in typ-II-glycogenosis (Pompe's disease, acid maltase deficiency) (author's transl)]. Gehlen W; Stefan H EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1978 Mar; 9(1):24-9. PubMed ID: 416945 [TBL] [Abstract][Full Text] [Related]
6. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. Beratis NG; LaBadie GU; Hirschhorn K J Clin Invest; 1978 Dec; 62(6):1264-74. PubMed ID: 34626 [TBL] [Abstract][Full Text] [Related]
7. [Pompe's disease. Part I: pathogenesis and clinical features]. Illés Z; Trauninger A Ideggyogy Sz; 2009 Jul; 62(7-8):231-43. PubMed ID: 19685701 [TBL] [Abstract][Full Text] [Related]
8. Infantile acid maltase deficiency. II. Muscle fiber hypertrophy and the ultrastructure of end-stage fibers. Griffin JL Virchows Arch B Cell Pathol Incl Mol Pathol; 1984; 45(1):37-50. PubMed ID: 6199886 [TBL] [Abstract][Full Text] [Related]
9. Muscular form of glycogenosis type II (Pompe's disease). Tanaka K; Shimazu S; Oya N; Tomisawa M; Kusunoki T; Soyama K; Ono E Pediatrics; 1979 Jan; 63(1):124-9. PubMed ID: 375166 [TBL] [Abstract][Full Text] [Related]
10. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency. Matsuishi T; Terasawa K; Yoshida I; Yano E; Yamashita F; Hidaka T; Ishihara O; Yoshino M; Nonaka I; Kurokawa T; Nakamura Y Neuropediatrics; 1982 Nov; 13(4):173-6. PubMed ID: 6818487 [TBL] [Abstract][Full Text] [Related]
11. [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]
13. Enzyme replacement therapy in late-onset Pompe's disease: a three-year follow-up. Winkel LP; Van den Hout JM; Kamphoven JH; Disseldorp JA; Remmerswaal M; Arts WF; Loonen MC; Vulto AG; Van Doorn PA; De Jong G; Hop W; Smit GP; Shapira SK; Boer MA; van Diggelen OP; Reuser AJ; Van der Ploeg AT Ann Neurol; 2004 Apr; 55(4):495-502. PubMed ID: 15048888 [TBL] [Abstract][Full Text] [Related]
14. 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; 72(2):135-42. PubMed ID: 9382133 [TBL] [Abstract][Full Text] [Related]
15. Glycogen storage disease type II in Israel. Bashan N; Potashnik R; Barash V; Gutman A; Moses SW Isr J Med Sci; 1988; 24(4-5):224-7. PubMed ID: 3132435 [TBL] [Abstract][Full Text] [Related]
16. Glycogenosis type II: the infantile- and late-onset acid maltase deficiency observed in one family. Koster JF; Busch HF; Slee RG; Van Weerden TW Clin Chim Acta; 1978 Aug; 87(3):451-3. PubMed ID: 28188 [TBL] [Abstract][Full Text] [Related]
17. 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]