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- 1. 乳児や小児の緑内障の概要 overview of glaucoma in infants and children
- 2. Congenital Zika virus infection: Clinical features, evaluation, and management of the neonate
- 3. 微細欠失症候群（12番～22番染色体） microdeletion syndromes chromosomes 12 to 22
- 4. エーラース・ダンロス症候群のマネージメントの概要 overview of the management of ehlers danlos syndromes
- 5. ファンコニー貧血の臨床症状と診断 clinical manifestations and diagnosis of fanconi anemia
English Journal
- Familial acorea, microphthalmia and cataract syndrome.
- Kondo H, Tahira T, Yamamoto K, Tawara A.SourceDepartment of Ophthalmology, University of Occupational and Environmental Health, , Kitakyushu, Japan.
- The British journal of ophthalmology.Br J Ophthalmol.2013 Sep;97(9):1155-60. doi: 10.1136/bjophthalmol-2013-303165. Epub 2013 Jul 5.
- PURPOSE: To describe the clinical features of members of a family with acorea, microphthalmia and cataract syndrome. In addition, to perform linkage analysis on family members to determine possible candidate genes.METHODS: Comprehensive ophthalmic examinations were performed on five affected members
- PMID 23832966
- Ocular genetic disease in the Middle East.
- Khan AO.SourceaDivision of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital bDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
- Current opinion in ophthalmology.Curr Opin Ophthalmol.2013 Sep;24(5):369-78. doi: 10.1097/ICU.0b013e3283638374.
- PURPOSE OF REVIEW: Centered on the Arabian Peninsula, the Middle East encompasses Northern Africa to Western Asia. Primarily Arab and historically tribal, populations from this region often practice customary intrafamilial marriage (consanguinity), intratribal marriage (endogamy), and a preference f
- PMID 23846189
- The Syndrome of Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus (MMCAT) Is Caused by Mutations in ADAMTS18.
- Aldahmesh MA, Alshammari MJ, Khan AO, Mohamed JY, Alhabib FA, Alkuraya FS.SourceDepartment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
- Human mutation.Hum Mutat.2013 Sep;34(9):1195-9. doi: 10.1002/humu.22374. Epub 2013 Jul 19.
- One of us recently described an apparently novel ocular syndrome characterized by microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) in a number of Saudi families. Consistent with the presumed pseudodominant inheritance in one of the original families, we show that MMCAT maps to a si
- PMID 23818446
Japanese Journal
- Endoscope-assisted vitrectomy for retinal detachment in an eye with microcornea
- Japanese journal of ophthalmology 56(6), 613-616, 2012-11-01
- NAID 10031126910
- Descemet stripping automated endothelial keratoplasty for microcornea
- Japanese journal of ophthalmology 56(5), 436-440, 2012-09-01
- NAID 10031039717
- CLINICAL INVESTIGATION : Descemet stripping automated endothelial keratoplasty for microcornea
- Japanese journal of ophthalmology : the official English-language journal of the Japanese Ophthalmological Society 56(5), 436-440, 2012-09
- NAID 40019415290
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