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4. Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype. Keulemans JL; Reuser AJ; Kroos MA; Willemsen R; Hermans MM; van den Ouweland AM; de Jong JG; Wevers RA; Renier WO; Schindler D; Coll MJ; Chabas A; Sakuraba H; Suzuki Y; van Diggelen OP J Med Genet; 1996 Jun; 33(6):458-64. PubMed ID: 8782044 [TBL] [Abstract][Full Text] [Related]
5. Structural and immunocytochemical studies on alpha-N-acetylgalactosaminidase deficiency (Schindler/Kanzaki disease). Sakuraba H; Matsuzawa F; Aikawa SI; Doi H; Kotani M; Nakada H; Fukushige T; Kanzaki T J Hum Genet; 2004; 49(1):1-8. PubMed ID: 14685826 [TBL] [Abstract][Full Text] [Related]
6. Characterization of clinical assays for leukocyte and fibroblast alpha-N-acetylgalactosaminidase activities for the diagnosis of alpha-N-acetylgalactosaminidase deficiency. Prence EM; Gleason J; Natowicz MR Clin Chim Acta; 1996 Mar; 247(1-2):167-73. PubMed ID: 8920235 [No Abstract] [Full Text] [Related]
7. alpha-N-acetylgalactosaminidase deficiency with mild clinical manifestations and difficult biochemical diagnosis. de Jong J; van den Berg C; Wijburg H; Willemsen R; van Diggelen O; Schindler D; Hoevenaars F; Wevers R J Pediatr; 1994 Sep; 125(3):385-91. PubMed ID: 8071745 [TBL] [Abstract][Full Text] [Related]
8. Studies on hexosaminidase C in cultured skin fibroblasts from patients with Sandhoff's disease. Broadhead DM; Besley GT Biochem Soc Trans; 1975; 3(2):247-50. PubMed ID: 236943 [No Abstract] [Full Text] [Related]
9. Post-translational processing reactions involved in the biosynthesis of lysosomal alpha-N-acetylgalactosaminidase in cultured human fibroblasts. Sweeley CC; Ledonne NC; Robbins PW Arch Biochem Biophys; 1983 May; 223(1):158-65. PubMed ID: 6859854 [TBL] [Abstract][Full Text] [Related]
10. An investigation into the glycolipid metabolism of alpha-N-acetylgalactosaminidase-deficient fibroblasts using native and artificial glycolipids. Klima B; Pohlentz G; Schindler D; Egge H Biol Chem Hoppe Seyler; 1992 Oct; 373(10):989-99. PubMed ID: 1418679 [TBL] [Abstract][Full Text] [Related]
11. Hexosaminidase A deficient adults: presence of alpha chain precursor in cultured skin fibroblasts. Frisch A; Baram D; Navon R Biochem Biophys Res Commun; 1984 Feb; 119(1):101-7. PubMed ID: 6231027 [TBL] [Abstract][Full Text] [Related]
12. Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb). Völker C; De Praeter CM; Hardt B; Breuer W; Kalz-Füller B; Van Coster RN; Bause E Glycobiology; 2002 Aug; 12(8):473-83. PubMed ID: 12145188 [TBL] [Abstract][Full Text] [Related]
13. Glycoscreening by on-line sheathless capillary electrophoresis/electrospray ionization-quadrupole time of flight-tandem mass spectrometry. Zamfir A; Peter-Katalinic J Electrophoresis; 2001 Aug; 22(12):2448-57. PubMed ID: 11519949 [TBL] [Abstract][Full Text] [Related]
14. alpha-N-acetylgalactosaminidase deficiency, a new lysosomal storage disorder. van Diggelen OP; Schindler D; Willemsen R; Boer M; Kleijer WJ; Huijmans JG; Blom W; Galjaard H J Inherit Metab Dis; 1988; 11(4):349-57. PubMed ID: 3149698 [TBL] [Abstract][Full Text] [Related]
15. Immunoelectron microscopic analysis of lysosomal deposits in alpha-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum. Kanda A; Tsuyama S; Murata F; Kodama K; Hirabayashi Y; Kanzaki T J Dermatol Sci; 2002 May; 29(1):42-8. PubMed ID: 12007720 [TBL] [Abstract][Full Text] [Related]
16. Human mannosidosis: in vitro and in vivo studies of cofactor supplementation. Grabowski GA; Walling L; Desnick RJ Birth Defects Orig Artic Ser; 1980; 16(1):319-34. PubMed ID: 7004518 [No Abstract] [Full Text] [Related]
17. A new case of alpha-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Ménière's syndrome and without mental retardation. Kodama K; Kobayashi H; Abe R; Ohkawara A; Yoshii N; Yotsumoto S; Fukushige T; Nagatsuka Y; Hirabayashi Y; Kanzaki T Br J Dermatol; 2001 Feb; 144(2):363-8. PubMed ID: 11251574 [TBL] [Abstract][Full Text] [Related]
18. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients. O'Brien JS Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742 [TBL] [Abstract][Full Text] [Related]
19. Lysosomal alpha-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria. Kanzaki T; Wang AM; Desnick RJ J Clin Invest; 1991 Aug; 88(2):707-11. PubMed ID: 1907616 [TBL] [Abstract][Full Text] [Related]
20. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts. Fluharty AL; Stevens RL; Sanders DL; Kihara H Biochem Biophys Res Commun; 1974 Jul; 59(2):455-61. PubMed ID: 4277366 [No Abstract] [Full Text] [Related] [Next] [New Search]