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BMC Research Notes|July 25, 2019
Polymorphisms rs693421 and rs2499601 at locus 1q43 and their haplotypes are not associated with primary open-angle glaucoma: a case-control studyAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.BMC Research Notes|October 18, 2018
Plexin domain containing 2 (PLXDC2) gene polymorphism rs7081455 may not influence POAG risk in a Saudi cohortAltaf A Kondkar, Tahira Sultan, Faisal A Almobarak, et al.Plos One|January 9, 2020
Association of endothelial nitric oxide synthase (NOS3) gene polymorphisms with primary open-angle glaucoma in a Saudi cohortAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.BMC Medical Genetics|July 10, 2020
Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi originAltaf A Kondkar, Tahira Sultan, Taif A Azad, et al.Journal of Ophthalmology|May 16, 2020
Elevated Plasma Level of 8-Hydroxy-2'-deoxyguanosine Is Associated with Primary Open-Angle GlaucomaAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.Biomed Research International|November 7, 2015
Assessment of the Knowledge and Attitudes of Saudi Mothers towards Newborn ScreeningAyman Al-Sulaiman, Altaf A Kondkar, Mohammad Y Saeedi, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|January 14, 2021
Association of rs12997 variant in the <i>ACVR1</i> gene: a member of bone morphogenic protein signaling pathway with primary open-angle glaucoma in a Saudi cohortAltaf A Kondkar, Taif A Azad, Tahira Sultan, et al.Molecular Vision|September 16, 2014
Keratoconus is associated with increased copy number of mitochondrial DNAKhaled K Abu-Amero, Altaf A Kondkar, Taif Anwar Azad, et al.Investigative Ophthalmology & Visual Science|April 12, 2014
Association of mitochondrial haplogroups H and R with keratoconus in Saudi Arabian patientsKhaled K Abu-Amero, Taif Anwar Azad, Tahira Sultan, et al.Molecular Diagnosis & Therapy|April 3, 2007
MEN1 935-1G>C splicing mutation in an Indian patient with multiple endocrine neoplasia type 1Rani Raghavan, Sudeep Shah, Altaf A Kondkar, et al.Pageof 9