Kanzaki T - Search Results

1

Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseases.

Asfaw B, Ledvinová J, Dobrovolńy R, Bakker HD, Desnick RJ, van Diggelen OP, de Jong JG, Kanzaki T, Chabas A, Maire I, Conzelmann E, Schindler D. Asfaw B, et al. Among authors: kanzaki t. J Lipid Res. 2002 Jul;43(7):1096-104. doi: 10.1194/jlr.m100423-jlr200. J Lipid Res. 2002. PMID: 12091494 Free article.

2

Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype.

Nakao S, Kodama C, Takenaka T, Tanaka A, Yasumoto Y, Yoshida A, Kanzaki T, Enriquez AL, Eng CM, Tanaka H, Tei C, Desnick RJ. Nakao S, et al. Among authors: kanzaki t. Kidney Int. 2003 Sep;64(3):801-7. doi: 10.1046/j.1523-1755.2003.00160.x. Kidney Int. 2003. PMID: 12911529 Free article.

3

[Schindler disease/Kanzaki disease].

Kanzaki T. Kanzaki T. Nihon Rinsho. 1995 Dec;53(12):2982-7. Nihon Rinsho. 1995. PMID: 8577046 Review. Japanese.

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. Sakuraba H, et al. Among authors: kanzaki t. J Hum Genet. 2004;49(1):1-8. doi: 10.1007/s10038-003-0098-z. Epub 2003 Dec 19. J Hum Genet. 2004. PMID: 14685826

5

[Schindler disease/Kanzaki disease [alpha-N-acetylgalactosaminidase deficiency]].

Kanzaki T. Kanzaki T. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):372-4. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645085 Review. Japanese. No abstract available.

6

Blood group A glycosphingolipid accumulation in the hair of patients with alpha-N-acetylgalactosaminidase deficiency.

Kimura A, Kanekura T, Saito Y, Sagawa K, Nosaka M, Kanzaki T, Tsuji T. Kimura A, et al. Among authors: kanzaki t. Life Sci. 2005 Mar 4;76(16):1817-24. doi: 10.1016/j.lfs.2004.09.027. Epub 2005 Jan 21. Life Sci. 2005. PMID: 15698859

7

[Skin Lesion in Fabry Disease].

Tsuboi K, Kanzaki T. Tsuboi K, et al. Among authors: kanzaki t. Brain Nerve. 2019 Apr;71(4):354-359. doi: 10.11477/mf.1416201275. Brain Nerve. 2019. PMID: 30988220 Japanese.

8

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. Kanda A, et al. Among authors: kanzaki t. J Dermatol Sci. 2002 May;29(1):42-8. doi: 10.1016/s0923-1811(02)00005-1. J Dermatol Sci. 2002. PMID: 12007720

9

Improved matrix-assisted laser desorption/ionization time-of-flight mass spectrometric method for identification of amino acid O-glycosides in patients with alpha-N-acetylgalactosaminidase deficiency.

Horiuchi M, Fukushige T, Saheki T, Kanzaki T. Horiuchi M, et al. Among authors: kanzaki t. Clin Chem. 2002 Oct;48(10):1798-9. Clin Chem. 2002. PMID: 12324503 No abstract available.

10

Neurologic manifestations of Kanzaki disease.

Umehara F, Matsumuro K, Kurono Y, Arimura K, Osame M, Kanzaki T. Umehara F, et al. Among authors: kanzaki t. Neurology. 2004 May 11;62(9):1604-6. doi: 10.1212/01.wnl.0000123116.96441.34. Neurology. 2004. PMID: 15136691

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