Matsumoto M - Search Results

1

Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778.

Matsumoto M, Hayasaka S, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A. Matsumoto M, et al. J Hum Genet. 1998;43(4):242-5. doi: 10.1007/s100380050081. J Hum Genet. 1998. PMID: 9852675

2

Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy.

Matsumoto M, Hayasaka S, Kadoi C, Hotta Y, Fujiki K, Fujimaki T, Takeda M, Ishida N, Endo S, Kanai A. Matsumoto M, et al. Ophthalmic Genet. 1999 Sep;20(3):153-60. doi: 10.1076/opge.20.3.153.2281. Ophthalmic Genet. 1999. PMID: 10520236

3

Rhodopsin gene codon 106 mutation (Gly-to-Arg) in a Japanese family with autosomal dominant retinitis pigmentosa.

Budu, Matsumoto M, Hayasaka S, Yamada T, Hayasaka Y. Budu, et al. Among authors: matsumoto m. Jpn J Ophthalmol. 2000 Nov-Dec;44(6):610-4. doi: 10.1016/s0021-5155(00)00286-0. Jpn J Ophthalmol. 2000. PMID: 11094174

4

Peripherin/RDS gene mutation (Pro210Leu) and polymorphisms in Japanese patients with retinal dystrophies.

Budu, Hayasaka S, Matsumoto M, Yamada T, Zhang XY, Hayasaka Y. Budu, et al. Among authors: matsumoto m. Jpn J Ophthalmol. 2001 Jul-Aug;45(4):355-8. doi: 10.1016/s0021-5155(01)00334-3. Jpn J Ophthalmol. 2001. PMID: 11485765

5

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. Yamada T, et al. Among authors: matsumoto m. J Hum Genet. 2001;46(12):733-6. doi: 10.1007/s100380170009. J Hum Genet. 2001. PMID: 11776388

6

1147 del A mutation in the arrestin gene in Japanese patients with Oguchi disease.

Yamada T, Matsumoto M, Kadoi C, Nagaki Y, Hayasaka Y, Hayasaka S. Yamada T, et al. Among authors: matsumoto m. Ophthalmic Genet. 1999 Jun;20(2):117-20. doi: 10.1076/opge.20.2.117.2293. Ophthalmic Genet. 1999. PMID: 10420197

7

REP-1 gene mutations in Japanese patients with choroideremia.

Fujiki K, Hotta Y, Hayakawa M, Saito A, Mashima Y, Mori M, Yoshii M, Murakami A, Matsumoto M, Hayasaka S, Tagami N, Isashiki Y, Ohba N, Kanai A. Fujiki K, et al. Among authors: matsumoto m. Graefes Arch Clin Exp Ophthalmol. 1999 Sep;237(9):735-40. doi: 10.1007/s004170050305. Graefes Arch Clin Exp Ophthalmol. 1999. PMID: 10447648

8

Bilateral congenital grouped pigmentation of the retina in one girl and bilateral congenital albinotic spots of the retina in her sister.

Kadoi C, Hayasaka S, Hayasaka Y, Matsumoto M, Nagaki Y. Kadoi C, et al. Among authors: matsumoto m. Retina. 1999;19(6):571-2. doi: 10.1097/00006982-199919060-00020. Retina. 1999. PMID: 10606465 No abstract available.

9

Serum methanol levels in subjects with or without optic nerve head disease.

Hayasaka Y, Hayasaka S, Hiraki S, Kadoi C, Nagaki Y, Matsumoto M. Hayasaka Y, et al. Among authors: matsumoto m. Ophthalmic Res. 2000 Nov-Dec;32(6):299-304. doi: 10.1159/000055629. Ophthalmic Res. 2000. PMID: 11015042

10

Management of traumatic cyclodialysis cleft associated with ocular hypotony.

Kato T, Hayasaka S, Nagaki Y, Matsumoto M. Kato T, et al. Among authors: matsumoto m. Ophthalmic Surg Lasers. 1999 Jun;30(6):469-72. Ophthalmic Surg Lasers. 1999. PMID: 10392735

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

7,853 results

Search Page

Filters