Detalhe da pesquisa
1.
Unraveling the genetic complexities of combined retinal dystrophy and hearing impairment.
Hum Genet
; 141(3-4): 785-803, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34148116
2.
Identification of genes involved in glaucoma pathogenesis using combined network analysis and empirical studies.
Hum Mol Genet
; 28(21): 3637-3663, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31518395
3.
Effects of intravitreal connective tissue growth factor neutralizing antibody on choroidal neovascular membrane-associated subretinal fibrosis.
Exp Eye Res
; 184: 286-295, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31029789
4.
Variable Expressivity of Wolfram Syndrome in a Family with Multiple Affected Subjects.
J Ophthalmic Vis Res
; 16(4): 602-610, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34840683
5.
Prenatal diagnosis of primary congenital glaucoma and histopathological features in a fetal globe with cytochrome p4501B1 mutations.
Eur J Ophthalmol
; : 11206721211051235, 2021 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34730456
6.
Multifunctional Theranostic Graphene Oxide Nanoflakes as MR Imaging Agents with Enhanced Photothermal and Radiosensitizing Properties.
ACS Appl Bio Mater
; 4(5): 4280-4291, 2021 05 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35006840
7.
Triple combination of heat, drug and radiation using alginate hydrogel co-loaded with gold nanoparticles and cisplatin for locally synergistic cancer therapy.
Int J Biol Macromol
; 158: 617-626, 2020 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32387354
8.
Gold nanoparticles promote a multimodal synergistic cancer therapy strategy by co-delivery of thermo-chemo-radio therapy.
Eur J Pharm Sci
; 145: 105235, 2020 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-31991226
9.
The First Inherited Retinal Disease Registry in Iran: Research Protocol and Results of a Pilot Study.
Arch Iran Med
; 23(7): 445-454, 2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32657595
10.
A novel PAX6 mutation causes congenital aniridia with or without retinal detachment.
Ophthalmic Genet
; 40(2): 146-149, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30985247
11.
PRPH2 mutation as the cause of various clinical manifestations in a family affected with inherited retinal dystrophy.
Ophthalmic Genet
; 40(5): 436-442, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31618092
12.
Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy.
Ophthalmic Genet
; 40(3): 259-266, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31215831