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Mutsuko Hayakawa

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Articles 6
Citations 151
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Recent Articles
1.
Jin Z, Hayakawa M, Murakami A, Nao-I N
Adv Exp Med Biol . 2007 Jan; 572:29-33. PMID: 17249551
Clinical research into mutations of the RPGR gene showed that lack of either the RCC1-like domain of the ORF15 causes X-linked retinitis pigmentosa. Thus, the ORF15 and RCC1-like domain play...
2.
Jin Z, Liu X, Hayakawa M, Murakami A, Nao-I N
Mol Vis . 2006 Nov; 12:1167-74. PMID: 17093403
Purpose: To identify mutations in RPGR and RP2 genes in a series of Japanese retinitis pigmentosa (RP) families and to determine the association between the phenotypic changes in patients/carriers and...
3.
Jin Z, Liu X, Uchida A, Vervoort R, Morishita K, Hayakawa M, et al.
Mol Vis . 2005 Jul; 11:535-41. PMID: 16052169
Purpose: To describe a macrodeletion spanning entire RCC1-like doman in the RPGR gene in one Japanese family with X-linked retinitis pigmentosa (XLRP). Methods: Clinical ophthalmologic examinations were performed and genomic...
4.
Li A, Jiao X, Munier F, Schorderet D, Yao W, Iwata F, et al.
Am J Hum Genet . 2004 Mar; 74(5):817-26. PMID: 15042513
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy characterized by multiple glistening intraretinal crystals scattered over the fundus, a characteristic degeneration of the retina, and sclerosis of...
5.
Amemiya K, Takahashi M, Nishida A, Matsumura M, Hayakawa M, Honda Y
Nippon Ganka Gakkai Zasshi . 2002 May; 106(4):236-42. PMID: 11979984
Purpose: To describe the histological and cytological findings in the epiretinal membrane around a macular hole. Case: A 24-year-old male patient with retinitis pigmentosa had had night blindness since childhood....
6.
Igarashi J, Shimizu T, Oguchi S, Yamashiro Y, Miyano T, Hayakawa M
Pediatr Int . 2002 Mar; 44(2):141-4. PMID: 11896870
Background: To evaluate the effect of n-3 polyunsaturated fatty acid (PUFA) deficiency on the development of retinal function in children with biliary atresia (BA), we examined serum fatty acid levels...