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

por Kondkar, Altaf A
Publicado no Appl Clin Genet (2021)

Utility of Circulating MicroRNAs as Clinical Biomarkers for Cardiovascular Diseases

por Kondkar, Altaf A., Abu-Amero, Khaled K.
Publicado no Biomed Res Int (2015)

An Updated Review on the Genetics of Primary Open Angle Glaucoma

por Abu-Amero, Khaled, Kondkar, Altaf A., Chalam, Kakarla V.
Publicado no Int J Mol Sci (2015)

Genetic analysis of Indian subjects with clinical features of possible type IIa hypercholesterolemia

por Kondkar, Altaf A., Nair, Kappiareth G., Ashavaid, Tester F.
Publicado no J Clin Lab Anal (2007)

Editorial: Molecular Mechanisms of Retinal Cell Degeneration and Regeneration

por Lobo, Glenn P., Biswal, Manas R., Kondkar, Altaf A.
Publicado no Front Cell Dev Biol (2021)

Resveratrol and Ophthalmic Diseases

por Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Publicado no Nutrients (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 no BMC Res Notes (2017)

Genetics of Keratoconus: Where Do We Stand?

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

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 no Saudi Med J (2015)

Sirtuins Expression and Their Role in Retinal Diseases

por Balaiya, Sankarathi, Abu-Amero, Khaled K., Kondkar, Altaf A., Chalam, Kakarla V.
Publicado no Oxid Med Cell Longev (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 no Clin Ophthalmol (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 em 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 em 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 no Neurosciences (Riyadh) (2016)

Transfection of Human Platelets with Short Interfering RNA

por Hong, Wei, Kondkar, Altaf A., Nagalla, Srikanth, Bergmeier, Wolfgang, Jin, Ying, Herman, Jay H., Bray, Paul F.
Publicado em 2011

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 no J Ophthalmol (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 em 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 no Biomed Res Int (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 no Clin Ophthalmol (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 no BMC Res Notes (2018)