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114 related items for PubMed ID: 20040332
1. Late onset glycogen storage disease type II with reducing body-like inclusions. Gayathri N, Yasha TC, Vani S, Taly AB, Nalini A, Shankar SK. Clin Neuropathol; 2010; 29(1):36-40. PubMed ID: 20040332 [Abstract] [Full Text] [Related]
5. The value of muscle biopsies in Pompe disease: identifying lipofuscin inclusions in juvenile- and adult-onset patients. Feeney EJ, Austin S, Chien YH, Mandel H, Schoser B, Prater S, Hwu WL, Ralston E, Kishnani PS, Raben N. Acta Neuropathol Commun; 2014 Jan 02; 2():2. PubMed ID: 24383498 [Abstract] [Full Text] [Related]
6. [Late onset liver involvement in type II glycogen storage disease: report of a case]. Kong Y, Wu HR, Fang PP, Han JZ, Zhang X, Gao J, Song XQ. Zhonghua Bing Li Xue Za Zhi; 2011 Aug 02; 40(8):567-8. PubMed ID: 22169653 [No Abstract] [Full Text] [Related]
11. Acid phosphatase-positive globular inclusions is a good diagnostic marker for two patients with adult-onset Pompe disease lacking disease specific pathology. Tsuburaya RS, Monma K, Oya Y, Nakayama T, Fukuda T, Sugie H, Hayashi YK, Nonaka I, Nishino I. Neuromuscul Disord; 2012 May 02; 22(5):389-93. PubMed ID: 22196155 [Abstract] [Full Text] [Related]
13. Pathology of skeletal muscle cells in adult-onset glycogenosis type II (Pompe disease): ultrastructural study. Lewandowska E, Wierzba-Bobrowicz T, Rola R, Modzelewska J, Stepień T, Lugowska A, Pasennik E, Ryglewicz D. Folia Neuropathol; 2008 May 02; 46(2):123-33. PubMed ID: 18587706 [Abstract] [Full Text] [Related]
15. Toward deconstructing the phenotype of late-onset Pompe disease. Schüller A, Wenninger S, Strigl-Pill N, Schoser B. Am J Med Genet C Semin Med Genet; 2012 Feb 15; 160C(1):80-8. PubMed ID: 22253010 [Abstract] [Full Text] [Related]
19. Fat and carbohydrate metabolism during exercise in late-onset Pompe disease. Preisler N, Laforet P, Madsen KL, Hansen RS, Lukacs Z, Ørngreen MC, Lacour A, Vissing J. Mol Genet Metab; 2012 Nov 15; 107(3):462-8. PubMed ID: 22981821 [Abstract] [Full Text] [Related]
20. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia. Ullrich K, Gröbe H, Korinthenberg R, von Bassewitz DB. Pathol Res Pract; 1986 Oct 15; 181(5):627-32. PubMed ID: 2947052 [Abstract] [Full Text] [Related] Page: [Next] [New Search]