WordNet

the whitish fibrous membrane (albuginea) that with the cornea forms the outer covering and protection of the eyeball (同)sclerotic coat

PrepTutorEJDIC

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 骨形成不全症：臨床的特徴および診断 osteogenesis imperfecta clinical features and diagnosis
2. エーラス・ダンロス症候群の臨床症状および診断 clinical manifestations and diagnosis of ehlers danlos syndromes
3. 児童虐待の整形外科的症状の鑑別診断 differential diagnosis of the orthopedic manifestations of child abuse
4. 小児における非抱合型高ビリルビン血症による黄疸の評価 evaluation of jaundice caused by unconjugated hyperbilirubinemia in children
5. 抗原虫治療 antiprotozoal therapies

Protective effects of sustained transscleral unoprostone delivery against retinal degeneration in S334ter rhodopsin mutant rats.

Nagai N1, Iwata S1, Kaji H2, Sampei K1, Katsukura Y1, Onami H1,3, Nishizawa M2, Nakazawa T3, Mashima Y4, Abe T5.
Journal of biomedical materials research. Part B, Applied biomaterials.J Biomed Mater Res B Appl Biomater.2016 Nov;104(8):1730-1737. doi: 10.1002/jbm.b.33522. Epub 2015 Sep 10.
It has been suggested that unoprostone isopropyl (UNO) has potent neuroprotective activity in the retina. The effect of sustained transscleral UNO delivery to the posterior segment of the eye on photoreceptor degeneration was evaluated. UNO was loaded into a device made of poly(ethyleneglycol) dimet
PMID 27753245

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.

Zhang H1, Yue H1, Wang C1, Hu W1, Gu J1, He J1, Fu W1, Hu Y1, Li M1, Zhang Z1.
Molecular medicine reports.Mol Med Rep.2016 Nov;14(5):4918-4926. doi: 10.3892/mmr.2016.5835. Epub 2016 Oct 12.
Osteogenesis imperfecta (OI) is an inherited connective tissue disorder characterized by brittle bone fractures. The aim of the present study was to investigate the pathogenic gene mutation spectrum and clinical manifestations of mutations in collagen type I, alpha 1 (COL1A1) and collagen type I, a
PMID 27748872

Corneal clouding, cataract, and colobomas with a novel missense mutation in B4GALT7-a review of eye anomalies in the linkeropathy syndromes.

Arunrut T1, Sabbadini M1, Jain M2, Machol K2, Scaglia F2, Slavotinek A3.
American journal of medical genetics. Part A.Am J Med Genet A.2016 Oct;170(10):2711-8. doi: 10.1002/ajmg.a.37809. Epub 2016 Jun 20.
We present a 5-year-old female with a distinctive phenotype comprising global developmental delays, pre- and post-natal growth restriction, striking joint laxity with soft skin, and scoliosis. She had a triangular facies, a prominent forehead, proptosis, a small nose, and a small jaw. Her ocular fin
PMID 27320698