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25. The liver in GM1 gangliosidosis types 1 and 2. A light and electron microscopical study. Petrelli M; Blair JD Arch Pathol; 1975 Feb; 99(2):111-6. PubMed ID: 1115681 [TBL] [Abstract][Full Text] [Related]
26. A suspected lysosomal storage disease in Abyssinian cats. Part II: histopathological and ultrastructural aspects. Lange AL; Bland van den Berg P; Baker MK J S Afr Vet Assoc; 1977 Oct; 48(3):201-9. PubMed ID: 599533 [TBL] [Abstract][Full Text] [Related]
27. Chronic GM1 gangliosidosis presenting as dystonia: I. Clinical and pathological features. Goldman JE; Katz D; Rapin I; Purpura DP; Suzuki K Ann Neurol; 1981 May; 9(5):465-75. PubMed ID: 6791574 [TBL] [Abstract][Full Text] [Related]
28. Abnormal neuronal metabolism and storage in mucopolysaccharidosis type VI (Maroteaux-Lamy) disease. Walkley SU; Thrall MA; Haskins ME; Mitchell TW; Wenger DA; Brown DE; Dial S; Seim H Neuropathol Appl Neurobiol; 2005 Oct; 31(5):536-44. PubMed ID: 16150124 [TBL] [Abstract][Full Text] [Related]
30. Lysosomal storage disorders in Thailand: the Siriraj experience. Wasant P; Wattanaweeradej S; Raksadawan N; Kolodny EH Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():54-8. PubMed ID: 8629143 [TBL] [Abstract][Full Text] [Related]
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32. Inactivation of GM1-ganglioside beta-galactosidase by a specific inhibitor: a model for ganglioside storage disease. Singer HS; Tiemeyer M; Slesinger PA; Sinnott ML Ann Neurol; 1987 May; 21(5):497-503. PubMed ID: 3035998 [TBL] [Abstract][Full Text] [Related]
33. Lipocalin-type prostaglandin D synthase is up-regulated in oligodendrocytes in lysosomal storage diseases and binds gangliosides. Mohri I; Taniike M; Okazaki I; Kagitani-Shimono K; Aritake K; Kanekiyo T; Yagi T; Takikita S; Kim HS; Urade Y; Suzuki K J Neurochem; 2006 May; 97(3):641-51. PubMed ID: 16515539 [TBL] [Abstract][Full Text] [Related]
34. [The role of ophthalmological examination in the diagnosis of gangliosidosis GM1]. Krzywińska-Zdeb E; Gizewska M; Modrzejewska M; Romanowska H; Stecewicz I; Pawłowska A; Tuziak M; Walczak M Klin Oczna; 2011; 113(7-9):266-9. PubMed ID: 22256571 [TBL] [Abstract][Full Text] [Related]
35. Ultrastructural study on a severe infantile sialidosis (beta-galactosidase-alpha-neuraminidase deficiency). Yamano T; Shimada M; Sugino H; Dezawa T; Koike M; Okada S; Yabuuchi H Neuropediatrics; 1985 May; 16(2):109-12. PubMed ID: 3925363 [TBL] [Abstract][Full Text] [Related]
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39. Adult type neuronal storage disease with neuraminidase deficiency. Miyatake T; Atsumi T; Obayashi T; Mizuno Y; Ando S; Ariga T; Matsui-Nakamura K; Yamada T Ann Neurol; 1979 Sep; 6(3):232-44. PubMed ID: 534422 [TBL] [Abstract][Full Text] [Related]
40. Beta-galactosidase deficiency in a Korat cat: a new form of feline GM1-gangliosidosis. De Maria R; Divari S; Bo S; Sonnio S; Lotti D; Capucchio MT; Castagnaro M Acta Neuropathol; 1998 Sep; 96(3):307-14. PubMed ID: 9754965 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]