Barmak Abdolrahimzadeh
Overview
Explore the profile of Barmak Abdolrahimzadeh including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
7
Citations
61
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Fragiotta S, Bassis L, Abdolrahimzadeh B, Marino A, Sepe M, Abdolrahimzadeh S
Int J Mol Sci
. 2024 Apr;
25(8).
PMID: 38674018
Long-lasting anti-vascular endothelial growth factor (anti-VEGF) agents have become an option to reduce treatment frequency, with ongoing research exploring optimal responses and safety profiles. This review delves into molecular targets,...
2.
Formisano M, Abdolrahimzadeh B, Mollo R, Bruni P, Malagola R, Abdolrahimzadeh S
J Curr Ophthalmol
. 2019 Jul;
31(2):242-249.
PMID: 31317109
Purpose: To present a patient with bilateral choroidal hemangioma in Sturge-Weber syndrome (SWS) and highlight multimodal imaging techniques for early detection and management of ocular alterations. Methods: A 37-year-old woman...
3.
Abdolrahimzadeh S, Parisi F, Abdolrahimzadeh B, Cruciani F
Acta Ophthalmol
. 2016 Aug;
94(8):e815-e816.
PMID: 27543268
No abstract available.
4.
Mannino G, Abdolrahimzadeh B, Calafiore S, Anselmi G, Mannino C, Lambiase A
Clin Ophthalmol
. 2016 Aug;
10:1453-9.
PMID: 27536058
Ultrasound biomicroscopy is a non-invasive imaging technique, which allows high-resolution evaluation of the anatomical features of the anterior segment of the eye regardless of optical media transparency. This technique provides...
5.
Abdolrahimzadeh B, Piraino D, Albanese G, Cruciani F, Rahimi S
Clin Ophthalmol
. 2016 Jun;
10:851-60.
PMID: 27257370
Neurofibromatosis (NF) is a multisystem disorder and tumor predisposition syndrome caused by genetic mutation on chromosome 17-17q11.2 in NF type 1 (NF1), and on chromosome 22-22q12.2 in NF type 2....
6.
Abdolrahimzadeh S, Piraino D, Scavella V, Abdolrahimzadeh B, Cruciani F, Gharbiya M, et al.
BMC Ophthalmol
. 2016 May;
16:60.
PMID: 27215604
Background: The purpose of this study was to evaluate the extension and traction effects of posterior vitreous detachment (PVD) complicated with retinal tears using spectral domain optical coherence tomography (OCT)...
7.
Plateroti A, Scavella V, Abdolrahimzadeh B, Plateroti R, Rahimi S
Semin Ophthalmol
. 2016 Apr;
32(4):524-528.
PMID: 27083007
Oculodermal melanocytosis (ODM) is a rare disease, which is characterized by hyperpigmentation of facial skin and several parts of the eye, such as the sclera, conjunctiva, cornea, iris, ciliary body,...