HN

Hadas Newman

Sackler Faculty of Medicine, Tel Aviv University

Affiliated withTel Aviv University

Research Area

Immunology and Infection

Biography

Hadas Newman has not added Biography.
If you are Hadas Newman and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 6	2017

Other Publications

Article	Year
Chiasmal cavernoma: a rare cause of acute visual loss improved by prompt surgery. Pediatric neurosurgery\| PubMed ID: 18703890	2008
Nonarteritic anterior ischemic optic neuropathy in a patient with primary acute angle-closure glaucoma. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie\| PubMed ID: 19020646	2008
Intraocular pressure changes in the contralateral eye after topical treatment: does an "ophthalmotonic consensual reaction" exist? The Israel Medical Association journal : IMAJ\| PubMed ID: 21287803	2010
Systemic bevacizumab (Avastin) for exudative retinal detachment secondary to choroidal melanoma. European journal of ophthalmology\| PubMed ID: 21445839	2011
Subfoveal choroidal melanoma: pretreatment characteristics and response to plaque radiation therapy. Archives of ophthalmology (Chicago, Ill. : 1960)\| PubMed ID: 21746980	2011
Involvement of CD24 in angiogenesis in a mouse model of oxygen-induced retinopathy. Current eye research\| PubMed ID: 22577772	2012
The prevalence of retinal and optical coherence tomography findings in preeclamptic women. Retina (Philadelphia, Pa.)\| PubMed ID: 24393833	2014
Visually evoked potentials in a patient with a fyodorov-zuev keratoprosthesis. Case reports in ophthalmology\| PubMed ID: 25759664	2015
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT). Human molecular genetics\| PubMed ID: 25859010	2015
An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy. Molecular vision\| PubMed ID: 26702251	2015
Partial thickness corneal tissue as a patch graft material for prevention of glaucoma drainage device exposure. BMC ophthalmology\| PubMed ID: 26920383	2016
Optical Coherence Tomography: An Adjunctive Tool for Differentiating between Choroidal Melanoma and Metastasis. Journal of ophthalmology\| PubMed ID: 26998354	2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. American journal of human genetics\| PubMed ID: 27588452	2016
Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone Syndrome. Investigative ophthalmology & visual science\| PubMed ID: 27732723	2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss. American journal of human genetics\| PubMed ID: 27814526	2016
Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coli. Protein expression and purification\| PubMed ID: 28167250	2017
Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL Genes. Genetic testing and molecular biomarkers\| PubMed ID: 28590779	2017