Fujishita S - Search Results

1

Treatment of experimental allergic encephalomyelitis by selective removal of CD4+ T cells.

Matsuo H, Ichinose K, Ohtsuru I, Fujishita S, Onodera H, Suematsu J, Yoshida M, Yamawaki N, Shibuya N. Matsuo H, et al. Among authors: fujishita s. Ther Apher. 1997 May;1(2):165-8. doi: 10.1111/j.1744-9987.1997.tb00034.x. Ther Apher. 1997. PMID: 10225764

2

Myasthenic crisis with delayed recovery after plasmapheresis.

Matsuo H, Goto H, Ohtsuru I, Izumoto H, Fukudome T, Fujishita S, Shibuya N. Matsuo H, et al. Among authors: fujishita s. Ther Apher. 1999 Nov;3(4):326-8. doi: 10.1046/j.1526-0968.1999.00205.x. Ther Apher. 1999. PMID: 10608729

3

[Complications with plasmapheresis].

Shibuya N, Fujishita S. Shibuya N, et al. Among authors: fujishita s. Nihon Rinsho. 1991 Dec;49 Suppl:567-71. Nihon Rinsho. 1991. PMID: 1808318 Japanese. No abstract available.

4

Correlation between clinical features and deletions of the gene for dystrophin in Duchenne muscular dystrophy.

Kanazawa H, Takashima H, Fujishita S, Shibuya N, Tamura T. Kanazawa H, et al. Among authors: fujishita s. Jpn J Med. 1991 Jan-Feb;30(1):1-4. doi: 10.2169/internalmedicine1962.30.1. Jpn J Med. 1991. PMID: 1865568 Free article.

5

[Microsatellite analysis of Duchenne muscular dystrophy].

Fujishita S, Shibuya N. Fujishita S, et al. Nihon Rinsho. 1997 Dec;55(12):3131-6. Nihon Rinsho. 1997. PMID: 9436423 Review. Japanese.

6

Acquired idiopathic generalized anhidrosis with isolated sudomotor neuropathy.

Miyazoe S, Matsuo H, Ohnishi A, Tajima F, Fujishita S, Ichinose K, Shibuya N. Miyazoe S, et al. Among authors: fujishita s. Ann Neurol. 1998 Sep;44(3):378-81. doi: 10.1002/ana.410440314. Ann Neurol. 1998. PMID: 9749605

7

Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.

Fujishita S, Shibuya N, Niikawa N, Nagataki S. Fujishita S, et al. Jinrui Idengaku Zasshi. 1991 Dec;36(4):317-24. doi: 10.1007/BF01883605. Jinrui Idengaku Zasshi. 1991. PMID: 1811098

8

Plasmapheresis changes lymphocyte subsets in myasthenia gravis.

Fujishita S, Motomura M, Ohishi K, Kanazawa H, Shibuya N. Fujishita S, et al. Prog Clin Biol Res. 1990;337:297-9. Prog Clin Biol Res. 1990. PMID: 2141172 No abstract available.

9

Different muscle specific promoter characteristics in two sibs with Duchenne muscular dystrophy.

Kondoh T, Fujishita S, Shibuya N, Matsumoto T. Kondoh T, et al. Among authors: fujishita s. J Med Genet. 1995 Apr;32(4):325-6. doi: 10.1136/jmg.32.4.325-a. J Med Genet. 1995. PMID: 7643370 Free PMC article. No abstract available.

10

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.

Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N. Sugino S, et al. Among authors: fujishita s. Am J Med Genet. 1989 Dec;34(4):555-61. doi: 10.1002/ajmg.1320340421. Am J Med Genet. 1989. PMID: 2576185

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