91 related articles for article (PubMed ID: 8577046)
1. [Schindler disease/Kanzaki disease].
Kanzaki T
Nihon Rinsho; 1995 Dec; 53(12):2982-7. PubMed ID: 8577046
[TBL] [Abstract][Full Text] [Related]
2. [Schindler disease/Kanzaki disease [alpha-N-acetylgalactosaminidase deficiency]].
Kanzaki T
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):372-4. PubMed ID: 9645085
[No Abstract] [Full Text] [Related]
3. Angiokeratoma corporis diffusum with glycopeptiduria due to deficient lysosomal alpha-N-acetylgalactosaminidase activity. Clinical, morphologic, and biochemical studies.
Kanzaki T; Yokota M; Irie F; Hirabayashi Y; Wang AM; Desnick RJ
Arch Dermatol; 1993 Apr; 129(4):460-5. PubMed ID: 8466216
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. [Lysosomal storage diseases with angiokeratoma corporis diffusum].
Kanzaki T
Nihon Rinsho; 1995 Dec; 53(12):3062-7. PubMed ID: 8577059
[TBL] [Abstract][Full Text] [Related]
8. [Schindler-disease/Kanzaki disease].
Sakuraba H
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):608-10. PubMed ID: 11528921
[No Abstract] [Full Text] [Related]
9. Mild phenotypic expression of alpha-N-acetylgalactosaminidase deficiency in two adult siblings.
Chabás A; Coll MJ; Aparicio M; Rodriguez Diaz E
J Inherit Metab Dis; 1994; 17(6):724-31. PubMed ID: 7707696
[TBL] [Abstract][Full Text] [Related]
10. Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy.
Wang AM; Schindler D; Desnick R
J Clin Invest; 1990 Nov; 86(5):1752-6. PubMed ID: 2243144
[TBL] [Abstract][Full Text] [Related]
11. Schindler disease: an inherited neuroaxonal dystrophy due to alpha-N-acetylgalactosaminidase deficiency.
Desnick RJ; Wang AM
J Inherit Metab Dis; 1990; 13(4):549-59. PubMed ID: 2122121
[TBL] [Abstract][Full Text] [Related]
12. A New Case of Schindler Disease.
Castro RG; Pérez AMG; Curto MCR; Álvarez JC; Ferreirós AC; Cuadros AV; Bueno DM; Fernández AJC
Eur J Case Rep Intern Med; 2019; 6(11):001269. PubMed ID: 31890708
[TBL] [Abstract][Full Text] [Related]
13. The molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes angiokeratoma corporis diffusum with glycopeptiduria.
Wang AM; Kanzaki T; Desnick RJ
J Clin Invest; 1994 Aug; 94(2):839-45. PubMed ID: 8040340
[TBL] [Abstract][Full Text] [Related]
14. Histopathologic and ultrastructural studies of angiokeratoma corporis diffusum in Kanzaki disease.
Yokota M; Koji M; Yotsumoto S
J Dermatol; 1995 Jan; 22(1):10-8. PubMed ID: 7897017
[TBL] [Abstract][Full Text] [Related]
15. Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: no association with neuroaxonal dystrophy?
Bakker HD; de Sonnaville ML; Vreken P; Abeling NG; Groener JE; Keulemans JL; van Diggelen OP
Eur J Hum Genet; 2001 Feb; 9(2):91-6. PubMed ID: 11313741
[TBL] [Abstract][Full Text] [Related]
16. Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency.
Schindler D; Bishop DF; Wolfe DE; Wang AM; Egge H; Lemieux RU; Desnick RJ
N Engl J Med; 1989 Jun; 320(26):1735-40. PubMed ID: 2733734
[No Abstract] [Full Text] [Related]
17. 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]
18. [Human geneticist from Würzburg discovers a new hereditary disease. Schindler disease: an autosome recessive neuro-axonal dystrophy].
Höhn H
Fortschr Med; 1991 Sep; 109(28):570-1. PubMed ID: 1757057
[No Abstract] [Full Text] [Related]
19. The 1.9 A structure of alpha-N-acetylgalactosaminidase: molecular basis of glycosidase deficiency diseases.
Garman SC; Hannick L; Zhu A; Garboczi DN
Structure; 2002 Mar; 10(3):425-34. PubMed ID: 12005440
[TBL] [Abstract][Full Text] [Related]
20. [Lysosomal diseases: an overview].
Suzuki Y
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):345-8. PubMed ID: 9645079
[No Abstract] [Full Text] [Related]
[Next] [New Search]
