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Acta Ophthalmologica, ISSN 1755-375X, 12/2018, Volume 96, Issue S261, pp. 55 - 56
Journal Article
Acta Ophthalmologica, ISSN 1755-375X, 12/2018, Volume 96, Issue S261, pp. 30 - 30
Journal Article
SCIENCE, ISSN 0036-8075, 06/2012, Volume 336, Issue 6086, pp. 1306 - 1310
Human UBIAD1 localizes to mitochondria and converts vitamin K-1 to vitamin K-2. Vitamin K-2 is best known as a cofactor in blood coagulation, but in bacteria... 
MENAQUINONE-4 | MULTIDISCIPLINARY SCIENCES | SCHNYDER | UBIAD1 GENE | MUTATIONS | DYSFUNCTION | IDENTIFICATION | DROSOPHILA-PINK1 | CRYSTALLINE CORNEAL-DYSTROPHY | PARKINSONS-DISEASE
Journal Article
Human Mutation, ISSN 1059-7794, 11/2010, Volume 31, Issue 11, pp. 1261 - 1268
  Homozygous mutations in the Borate Cotransporter SLC4A11 cause two early-onset corneal dystrophies: congenital hereditary endothelial dystrophy (CHED) and... 
SLC4A11 | Anterior segment | Corneal endothelium | Fuchs corneal dystrophy
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 03/2019, Volume 40, Issue 2, pp. 91 - 98
Background: Corneal Dystrophy and Perceptive Deafness (CDPD) or Harboyan syndrome is an autosomal recessive rare disorder, characterized by congenital corneal... 
corneal dystrophy | Harboyan | CDPD | SLC4A11 gene | Endothelium
Journal Article
International Journal of Clinical Practice, ISSN 1368-5031, 06/2019, Volume 73, Issue 6, pp. e13320 - n/a
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 09/2018, Volume 59, Issue 11, pp. 4748 - 4754
To assess the occurrence and diagnostic performance of nine single-nucleotide variants (SNVs) in the TCF4, SLC4A11, LOXHD1, and AGBL1 genes and the CTG18.1... 
Molecular markers | Tcf4 | Microsatellite expansion | Corneal dystrophy | Fuchs dystrophy | Index Medicus
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 2019, p. bjophthalmol-2018-313809
BACKGROUND/AIMSTo investigate the efficacy of therapeutic soft contact lenses (SCLs) in gelatinous drop-like corneal dystrophy (GDLD) management.METHODSThis... 
visual acuity | corneal dystrophy | soft contact lens | nodular lesions | surgical intervention
Journal Article
Journal of Biomedical Optics, ISSN 1083-3668, 04/2019, Volume 24, Issue 4, pp. 1 - 17
To identify the microstructural modification of the corneal layers during the course of the disease, optical technologies have been pushing the boundary of... 
Corneal disease | Fuchs endothelial corneal dystrophy | Ophthalmology | Microscopy | Optical coherence tomography | Corneal imaging
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 09/2018, Volume 136, Issue 9, p. 969
Fuchs endothelial corneal dystrophy (FECD) is a hereditary degenerative condition that is characterized by the progression of focal excrescences in the... 
Edema | Cornea | Genetic disorders | Transplants & implants | Corneal dystrophy | Eye diseases | Transplantation | Dystrophy | Endothelial cells
Journal Article
Experimental Eye Research, ISSN 0014-4835, 06/2019, pp. 107696 - 107696
Mutations associated with posterior polymorphous corneal dystrophy (PPCD) have been identified in three genes: ZEB1 (zinc-finger E-box binding homeobox 1)... 
Journal Article
JAMA Ophthalmology, ISSN 2168-6165, 08/2018, Volume 136, Issue 8, p. 893
There are several major etiologies of corneal endothelial dysfunction that eventually result in the development of bullous keratopathy (BK), such as... 
Glaucoma | Edema | Cornea | Corneal dystrophy | Surgery | Eye diseases | Ophthalmology | Dystrophy | Endothelial cells
Journal Article
Ophthalmologe, ISSN 0941-293X, 03/2019, Volume 116, Issue 3, pp. 228 - 235
Journal Article
Офтальмохирургия, ISSN 0235-4160, 04/2018, Issue 1, pp. 19 - 25
Purpose. The purpose of this comparative study was to assess the efficiency and safety of the Femtosecond Laser Assisted Cataract Surgery (FLACS) and the... 
femtosecond laser | Fuchs endothelial corneal dystrophy | phacoemulsification
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 06/2018, Volume 235, Issue 6, pp. 702 - 708
Journal Article
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