Detalhe da pesquisa
1.
Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry.
Mol Vis
; 29: 1-12, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37287645
2.
THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.
Retina
; 42(7): 1364-1369, 2022 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35250012
3.
UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association.
Retina
; 41(12): 2462-2471, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34369440
4.
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC).
Hum Mutat
; 41(1): 140-149, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31456290
5.
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Genet Med
; 22(7): 1235-1246, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32307445
6.
Effect of light and diurnal variation on macular thickness in X-linked retinoschisis: a case series.
Graefes Arch Clin Exp Ophthalmol
; 258(3): 529-536, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31897705
7.
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Am J Hum Genet
; 99(3): 777-784, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588452
8.
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES].
Harefuah
; 158(2): 91-95, 2019 Feb.
Artigo
em Hebraico
| MEDLINE | ID: mdl-30779484
9.
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
Ophthalmology
; 125(5): 725-734, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29276052
10.
Prevalence of choroidal nevus and retinal pigment epithelial alterations in vitiligo patients.
Graefes Arch Clin Exp Ophthalmol
; 256(5): 927-933, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29549426
11.
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT).
Hum Mol Genet
; 24(13): 3742-51, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25859010
12.
Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coli.
Protein Expr Purif
; 132: 138-142, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28167250
14.
Partial thickness corneal tissue as a patch graft material for prevention of glaucoma drainage device exposure.
BMC Ophthalmol
; 16: 20, 2016 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-26920383
15.
An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy.
Mol Vis
; 21: 1295-306, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26702251
16.
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.
Am J Hum Genet
; 99(5): 1222-1223, 2016 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27814526
17.
The prevalence of retinal and optical coherence tomography findings in preeclamptic women.
Retina
; 34(7): 1376-83, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24393833
18.
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population.
JAMA Ophthalmol
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753338
19.
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population.
Invest Ophthalmol Vis Sci
; 65(2): 39, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38411968
20.
Intraocular pressure changes in the contralateral eye after topical treatment: does an "ophthalmotonic consensual reaction" exist?
Isr Med Assoc J
; 12(9): 568-71, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21287803