Updates on Genes and Genetic Mechanisms Implicated in Primary Angle-Closure Glaucoma

por Kondkar, Altaf A
Publicado 2021

Utility of Circulating MicroRNAs as Clinical Biomarkers for Cardiovascular Diseases

por Kondkar, Altaf A., Abu-Amero, Khaled K.
Publicado 2015

An Updated Review on the Genetics of Primary Open Angle Glaucoma

por Abu-Amero, Khaled, Kondkar, Altaf A., Chalam, Kakarla V.
Publicado 2015

Editorial: Molecular Mechanisms of Retinal Cell Degeneration and Regeneration

por Lobo, Glenn P., Biswal, Manas R., Kondkar, Altaf A.
Publicado 2021

Resveratrol and Ophthalmic Diseases

por Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Publicado 2016

A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles

por Abu-Amero, Khaled K., Kondkar, Altaf A., Khan, Arif O.
Publicado 2017

Genetics of Keratoconus: Where Do We Stand?

por Abu-Amero, Khaled K., Al-Muammar, Abdulrahman M., Kondkar, Altaf A.
Publicado 2014

Editorial: Inherited retinal dystrophies: a light at the end of the tunnel?

por Perkins, Brian D., Lobo, Glenn P., Kondkar, Altaf A., Millan, Jose M.
Publicado 2023

A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia

por Mohamed, Sarar, Hamad, Muddathir H., Kondkar, Altaf A., Abu-Amero, Khaled K.
Publicado 2015

Sirtuins Expression and Their Role in Retinal Diseases

por Balaiya, Sankarathi, Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Publicado 2017

Analysis of CYP1B1 sequence alterations in patients with primary open-angle glaucoma of Saudi origin

por Abu-Amero, Khaled K, Sultan, Tahira, Al-Obeidan, Saleh A, Kondkar, Altaf A
Publicado 2018

Decreased total antioxidants status in the plasma of patients with pseudoexfoliation glaucoma

por Abu-Amero, Khaled K., Kondkar, Altaf A., Mousa, Ahmed, Osman, Essam A., Al-Obeidan, Saleh A.
Publicado 2011

Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohort

por Abu-Amero, Khaled K., Kondkar, Altaf A., Mousa, Ahmed, Osman, Essam A., Al-Obeidan, Saleh A.
Publicado 2012

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

por Abu-Amero, Khaled K., Kondkar, Altaf A., Hellani, Ali M., Bosley, Thomas M., Khan, Arif O.
Publicado 2016

Increased Plasma Levels of 8-Hydroxy-2′-deoxyguanosine (8-OHdG) in Patients with Pseudoexfoliation Glaucoma

por Kondkar, Altaf A., Sultan, Tahira, Azad, Taif A., Tabussum, Lubna, Osman, Essam A., Al-Obeidan, Saleh A.
Publicado 2019

Keratoconus is associated with increased copy number of mitochondrial DNA

por Abu-Amero, Khaled. K., Kondkar, Altaf A., Azad, Taif Anwar, Sultan, Tahira, Kalantan, Hatem, Al-Muammar, Abdulrahman M.
Publicado 2014

Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn Screening

por Al-Sulaiman, Ayman, Kondkar, Altaf A., Saeedi, Mohammad Y., Saadallah, Amal, Al-Odaib, Ali, Abu-Amero, Khaled K.
Publicado 2015

Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma

por Kondkar, Altaf A, Sultan, Tahira, Almobarak, Faisal A, Kalantan, Hatem, Al-Obeidan, Saleh A, Abu-Amero, Khaled K
Publicado 2018

Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohort

por Kondkar, Altaf A., Sultan, Tahira, Almobarak, Faisal A., Kalantan, Hatem, Abu-Amero, Khaled K., Al-Obeidan, Saleh A.
Publicado 2018

Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case–control study

por Kondkar, Altaf A., Azad, Taif A., Sultan, Tahira, Al-Mobarak, Faisal A., Kalantan, Hatem, Al-Obeidan, Saleh A.
Publicado 2019