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26. Study of alpha-D-glucosidase activity in patients with Pompe's disease. Lin CY; Hwang B; Hsiao KJ; Jin YR Taiwan Yi Xue Hui Za Zhi; 1986 Aug; 85(8):766-70. PubMed ID: 3540186 [No Abstract] [Full Text] [Related]
27. Pompe's disease: report of a neonatal case. Chen MR; Lin SP; Loo JH; Sung TC; Chen BF Taiwan Yi Xue Hui Za Zhi; 1988 Oct; 87(10):1017-20. PubMed ID: 3149289 [No Abstract] [Full Text] [Related]
28. Thin-layer chromatography of oligosaccharides in urine as a rapid indication for the diagnosis of lysosomal acid maltase deficiency (Pompe's disease). Blom W; Luteyn JC; Kelholt-Dijkman HH; Huijmans JG; Loonen MC Clin Chim Acta; 1983 Oct; 134(1-2):221-7. PubMed ID: 6418415 [No Abstract] [Full Text] [Related]
30. The first trimester prenatal diagnosis of Pompe's disease at risk. Ezaki M; Sugiyama K; Wada Y; Suzumori K Jinrui Idengaku Zasshi; 1987 Sep; 32(3):267-9. PubMed ID: 3329254 [No Abstract] [Full Text] [Related]
31. Searching for molecular abnormalities in genetic diseases by the use of a double labeling technique. II. Deficiency of a basic protein in fibroblasts of patients with Pompe's disease. Pena SD; Quilliam NM; Hamerton JL; Wrogemann K Pediatr Res; 1978 Sep; 12(9):894-8. PubMed ID: 362358 [TBL] [Abstract][Full Text] [Related]
33. Adeno-associated virus-mediated transfer of human acid maltase gene results in a transient reduction of glycogen accumulation in muscle of Japanese quail with acid maltase deficiency. Lin CY; Ho CH; Hsieh YH; Kikuchi T Gene Ther; 2002 May; 9(9):554-63. PubMed ID: 11973631 [TBL] [Abstract][Full Text] [Related]
34. [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]
35. Replacing acid alpha-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers. Raben N; Fukuda T; Gilbert AL; de Jong D; Thurberg BL; Mattaliano RJ; Meikle P; Hopwood JJ; Nagashima K; Nagaraju K; Plotz PH Mol Ther; 2005 Jan; 11(1):48-56. PubMed ID: 15585405 [TBL] [Abstract][Full Text] [Related]
36. Identification of a de novo point mutation resulting in infantile form of Pompe's disease. Lin CY; Shieh JJ Biochem Biophys Res Commun; 1995 Mar; 208(2):886-93. PubMed ID: 7695647 [TBL] [Abstract][Full Text] [Related]
37. [Enzyme replacement therapy in Pompe's disease]. Merk T; Wibmer T; Schumann C; Krüger S Med Klin (Munich); 2007 Jul; 102(7):570-3. PubMed ID: 17634875 [TBL] [Abstract][Full Text] [Related]
38. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls]. Matsuoka Y; Hirayama M; Senda Y; Matsui T Rinsho Shinkeigaku; 1985 Jan; 25(1):39-45. PubMed ID: 3922655 [No Abstract] [Full Text] [Related]
39. Biosynthesis of acid alpha-glucosidase in late-onset forms of glycogenosis type II (Pompe's disease). Steckel F; Gieselmann V; Waheed A; Hasilik A; von Figura K; Oude Elferink R; Kalsbeek R; Tager JM FEBS Lett; 1982 Dec; 150(1):69-76. PubMed ID: 6761145 [TBL] [Abstract][Full Text] [Related]
40. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation. Iwamasa T; Ninomiya N; Fukuda S; Hamada T; Hirashima M; Osame M Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]