These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
297 related items for PubMed ID: 6777881
1. 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 22; 58(21):860-2. PubMed ID: 6777881 [Abstract] [Full Text] [Related]
2. 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 22; 30(4):298-301. PubMed ID: 3098466 [Abstract] [Full Text] [Related]
3. Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy. Besançon AM, Castelnau L, Nicolesco H, Dumez Y, Poenaru L. Clin Genet; 1985 May 22; 27(5):479-82. PubMed ID: 3891160 [Abstract] [Full Text] [Related]
15. Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblasts. Reuser AJ, Kroos M, Willemsen R, Swallow D, Tager JM, Galjaard H. J Clin Invest; 1987 Jun 22; 79(6):1689-99. PubMed ID: 3108320 [Abstract] [Full Text] [Related]
16. [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 22; 81(1):109-14. PubMed ID: 3130016 [Abstract] [Full Text] [Related]
17. Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease). Pokorny KS, Ritch R, Friedman AH, Desnick RJ. Invest Ophthalmol Vis Sci; 1982 Jan 22; 22(1):25-31. PubMed ID: 6948796 [Abstract] [Full Text] [Related]
18. 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 22; 63(1):124-9. PubMed ID: 375166 [Abstract] [Full Text] [Related]
19. 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 22; 12(9):894-8. PubMed ID: 362358 [Abstract] [Full Text] [Related]
20. 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 31; 134(1-2):221-7. PubMed ID: 6418415 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]