OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484
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Published in Japanese journal of ophthalmology (01.07.2003)
Published in Japanese journal of ophthalmology (01.07.2003)
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Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome
Yamada, T, Hayasaka, S, Matsumoto, M, Budu, Esa, T, Hayasaka, Y, Endo, M
Published in Journal of human genetics (01.01.2001)
Published in Journal of human genetics (01.01.2001)
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Congenital hypertrophy of the retinal pigment epithelium in a man with nevus of Ota
HAYASAKA, Yoriko, HAYASAKA, Seiji, NAGAKI, Yasunori, ENDO, Machi
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Published in Annals of ophthalmology (01.03.2003)
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Recurrent vitreous hemorrhage in boys with prepapillary arterial loops
ENDO, Machi, HAYASAKA, Seiji, YASUNORI, NAGAKI, MATSUMOTO, Masayuki, HAYASAKA, Yoriko
Published in Annals of ophthalmology (01.09.2003)
Published in Annals of ophthalmology (01.09.2003)
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CHARGE association in a 19-year-old woman
ENDO, Machi, HAYASAKA, Seiji, YANAGISAWA, Shuichiro, NAGAKI, Yasunori, MATSUMOTO, Masayuki, HAYASAKA, Yoriko
Published in Annals of ophthalmology (01.12.2002)
Published in Annals of ophthalmology (01.12.2002)
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VERFAHREN ZUR ADSORPTIVEN TRENNUNG VON DICHLORTOLUEN
KANNO, SUEO, HANE, YUICHI, KORIYAMA-SHI FUKUSHIMA-KEN, JP, ENDO, TOSHIYUKI, OSE-MACHI KORIYAMA-SHI FUKUSHIMA-KEN, JP, KANESHIKI, TOSHITAKA, TOKYO, JP, ABE, YOSHIHIKO, FUKUYAMA-MACHI KORIYAMA-SHI FUKUSHIMA-, JP, HANEDA, TADAYOSHI
Year of Publication 28.01.1993
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Year of Publication 28.01.1993
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