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22. [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 16; 79(5):227-31. PubMed ID: 6755088 [No Abstract] [Full Text] [Related]
23. 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]
24. Protein turnover in acid maltase deficiency before and after treatment with a high protein diet. Umpleby AM, Wiles CM, Trend PS, Scobie IN, Macleod AF, Spencer GT, Sonksen PH. J Neurol Neurosurg Psychiatry; 1987 May 31; 50(5):587-92. PubMed ID: 3108456 [Abstract] [Full Text] [Related]
30. [Ichthyosiform scaling in alpha-1,4-glucosidase deficiency]. Gebhart W, Mainitz M, Jurecka W, Niebauer G, Paschke E, Stöckler S, Sluga E. Hautarzt; 1988 Apr 31; 39(4):228-32. PubMed ID: 3290163 [Abstract] [Full Text] [Related]
31. Effect of acid maltase deficiency on the endosomal/lysosomal system and glucose transporter 4. Orth M, Mundegar RR. Neuromuscul Disord; 2003 Jan 31; 13(1):49-54. PubMed ID: 12467732 [Abstract] [Full Text] [Related]
32. Adult-onset acid maltase deficiency in siblings. Miyamoto Y, Etoh Y, Joh R, Noda K, Ohya I, Morimatsu M. Acta Pathol Jpn; 1985 Nov 31; 35(6):1533-42. PubMed ID: 3937437 [Abstract] [Full Text] [Related]
33. The effect of age on biochemical and morphological changes in the semitendinosus muscle of cattle with generalized glycogenosis type II. Howell JM, Dorling PR, Cook RD. Neuropathol Appl Neurobiol; 1984 Nov 31; 10(4):255-66. PubMed ID: 6435005 [Abstract] [Full Text] [Related]
34. 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 31; 15(6):601-4. PubMed ID: 6347982 [No Abstract] [Full Text] [Related]
35. [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 31; 81(1):109-14. PubMed ID: 3130016 [Abstract] [Full Text] [Related]
36. Acid maltase deficiency--Pompe's disease. Jamil S, Ahmed S, Tariq M. J Pak Med Assoc; 2011 Aug 31; 61(8):821-3. PubMed ID: 22356012 [Abstract] [Full Text] [Related]
37. Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures. Miranda AF, Shanske S, Hays AP, DiMauro S. Arch Neurol; 1985 Apr 31; 42(4):371-3. PubMed ID: 3921010 [Abstract] [Full Text] [Related]
38. Apparent normal leukocyte acid maltase activity in glycogen storage disease type II (Pompe's disease). Potter JL, Robinson HB, Kramer JD, Schafter IA. Clin Chem; 1980 Dec 31; 26(13):1914-5. PubMed ID: 7002367 [Abstract] [Full Text] [Related]
39. "Reducing body"-like inclusions in skeletal muscle in childhood-onset acid maltase deficiency. Jay V, Christodoulou J, Mercer-Connolly A, McInnes RR. Acta Neuropathol; 1992 Dec 31; 85(1):111-5. PubMed ID: 1337420 [Abstract] [Full Text] [Related]
40. A new variant form of hepatic glycogenosis with acid maltase deficiency. Ninomiya N, Terashima T, Iwamasa T, Matsuda I. Jinrui Idengaku Zasshi; 1984 Jun 31; 29(2):113-9. PubMed ID: 6439921 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]