Ikeya K - Search Results

1

Hyperzincemia with systemic inflammation: a heritable disorder of calprotectin metabolism with rheumatic manifestations?

Saito Y, Saito K, Hirano Y, Ikeya K, Suzuki H, Shishikura K, Manno S, Takakuwa Y, Nakagawa K, Iwasa A, Fujikawa S, Moriya M, Mizoguchi N, Golden BE, Osawa M. Saito Y, et al. Among authors: ikeya k. J Pediatr. 2002 Feb;140(2):267-9. doi: 10.1067/mpd.2002.121699. J Pediatr. 2002. PMID: 11865286

2

Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigation.

Yamamoto T, Shibata N, Kanazawa M, Kobayashi M, Komori T, Ikeya K, Kondo E, Saito K, Osawa M. Yamamoto T, et al. Among authors: ikeya k. Acta Neuropathol. 1997 Aug;94(2):173-9. doi: 10.1007/s004010050690. Acta Neuropathol. 1997. PMID: 9255393

3

Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy.

Saito K, Osawa M, Wang ZP, Ikeya K, Fukuyama Y, Kondo-Iida E, Toda T, Ohashi H, Kurosawa K, Wakai S, Kaneko K. Saito K, et al. Among authors: ikeya k. Am J Med Genet. 2000 May 29;92(3):184-90. doi: 10.1002/(sici)1096-8628(20000529)92:3<184::aid-ajmg5>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10817652

4

Somatic mosaicism for a DMD gene deletion.

Saito K, Ikeya K, Kondo E, Komine S, Komine M, Osawa M, Aikawa E, Fukuyama Y. Saito K, et al. Among authors: ikeya k. Am J Med Genet. 1995 Mar 13;56(1):80-6. doi: 10.1002/ajmg.1320560118. Am J Med Genet. 1995. PMID: 7747792

5

[Genetic counselling for Duchenne muscular dystrophy].

Ousawa M, Saito K, Ikeya K, Fukuyama Y. Ousawa M, et al. Among authors: ikeya k. No To Shinkei. 1991 May;43(5):429-41. No To Shinkei. 1991. PMID: 1910929 Japanese. No abstract available.

6

Prenatal diagnosis of Fukuyama type congenital muscular dystrophy in eight Japanese families by haplotype analysis using new markers closest to the gene.

Saito K, Kondo-Iida E, Kawakita Y, Juan D, Ikeya K, Osawa M, Fukuyama Y, Toda T, Nakabayashi M, Yamamoto T, Kobayashi M. Saito K, et al. Among authors: ikeya k. Am J Med Genet. 1998 May 26;77(4):310-6. Am J Med Genet. 1998. PMID: 9600742

7

[Molecular genetics of Duchenne/Becker muscular dystrophy].

Saito K, Ikeya K, Kondo E, Yamauchi A, Komine S, Fukuyama Y. Saito K, et al. Among authors: ikeya k. Nihon Rinsho. 1993 Sep;51(9):2420-7. Nihon Rinsho. 1993. PMID: 8411723 Review. Japanese.

8

[Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA].

Saito K, Tanaka A, Harada T, Ikeya K, Fukuyama Y, Arahata K, Sugita H, Osawa M, Shishikura K, Suzuki H. Saito K, et al. Among authors: ikeya k. No To Hattatsu. 1989 Jul;21(4):361-8. No To Hattatsu. 1989. PMID: 2675944 Japanese.

9

[Clinical significance of dystrophin test for patients with various neuromuscular diseases--immunofluorescence and immunoblot analyses of dystrophin abnormalities].

Ikeya K, Saito K, Yamauchi A, Kondo E, Komine S, Ikenaka H, Mishima M, Takahashi R, Harada T, Fukuyama Y. Ikeya K, et al. No To Hattatsu. 1993 Jul;25(4):328-34. No To Hattatsu. 1993. PMID: 8338694 Japanese.

10

[Home-stay respiratory management of a child with nemaline myopathy by using a negative pressure-controlled respirator].

Ikeya K, Kajiyama M, Hirasawa K, Ohsawa M, Shishikura K, Suzuki H, Fukuyama Y. Ikeya K, et al. No To Hattatsu. 1988;20(5):423-8. No To Hattatsu. 1988. PMID: 3224016 Japanese. No abstract available.

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