WordNet

bring disorder to (同)disarray
a physical condition in which there is a disturbance of normal functioning; "the doctor prescribed some medicine for the disorder"; "everyone gets stomach upsets from time to time" (同)upset
a disturbance of the peace or of public order
the transparent dome-shaped anterior portion of the outer covering of the eye; it covers the iris and pupil and is continuous with the sclera
of or related to the cornea
of or relating to or located in the endothelium
not arranged in order (同)unordered

PrepTutorEJDIC

〈U〉『無秩序』,混乱,乱雑(confusion) / 《しばしば複数形で》(社会的・政治的な)粉争,騒動 / 〈C〉(肉体的・精神的な)不調,異常,障害 / …‘の'秩序を乱す / 〈心身〉‘に'異常を起こさせる
(眼球の)角膜
角膜の

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. 単純ヘルペス性角膜炎 herpes simplex keratitis
2. 肝移植：急性細胞性拒絶反応の診断 liver transplantation diagnosis of acute cellular rejection
3. 肝移植後のC型肝炎ウイルス感染の再発 recurrence of hepatitis c virus infection following liver transplantation
4. 円錐角膜 keratoconus
5. 関節リウマチの眼症状 ocular manifestations of rheumatoid arthritis

Molecular and clinical studies in five index cases with novel mutations in the GLA gene.

Zizzo C1, Monte I2, Pisani A3, Fatuzzo P4, Riccio E3, Rodolico MS5, Colomba P6, Uva M7, Cammarata G6, Alessandro R8, Iemolo F6, Duro G6.
Gene.Gene.2016 Mar 1;578(1):100-4. doi: 10.1016/j.gene.2015.12.024. Epub 2015 Dec 12.
Fabry disease is a metabolic and lysosomal storage disorder caused by the functional defect of the α-galactosidase A enzyme; this defect is due to mutations in the GLA gene, that is composed of seven exons and is located on the long arm of the X-chromosome (Xq21-22). The enzymatic deficit is respon
PMID 26691501

Ramamurthy S1, Reddy JC2, Vaddavalli PK1, Ali MH3, Garg P1.
American journal of ophthalmology.Am J Ophthalmol.2016 Feb;162:83-88.e2. doi: 10.1016/j.ajo.2015.11.004. Epub 2015 Nov 10.
PURPOSE: To analyze clinical outcomes of repeat optical penetrating (PK) or endothelial keratoplasty (EK) after failed therapeutic keratoplasty (TPK).DESIGN: Retrospective consecutive, comparative, interventional case series.METHODS: setting: LV Prasad Eye Institute, Hyderabad, India.STUDY POPULATIO
PMID 26558523

Pathophysiology of Corneal Dystrophies: From Cellular Genetic Alteration to Clinical Findings.

Sacchetti M1, Macchi I2, Tiezzi A3, La Cava M3, Massaro-Giordano G4, Lambiase A3.
Journal of cellular physiology.J Cell Physiol.2016 Feb;231(2):261-9. doi: 10.1002/jcp.25082.
Corneal dystrophies are a heterogeneous group of bilateral, inherited, rare diseases characterized by slowly progressive corneal opacities, that lead to visual impairment. Most of them have an autosomal dominant pattern of inheritance with variable expressivity, but new mutations have been described
PMID 26104822