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Alternative Therapies in Health and Medicine|February 17, 2025
A Randomized Open-Labelled Clinical Study on the Efficacy of Polyherbal Oral and Topical Unani Formulations (Majoon and Tila) Versus Tentex Forte and Himcolin in Erectile DysfunctionS M Shadab Kazmi, M Aleemuddin Quamri, Wasim Ahmad, et al.Genetic Testing and Molecular Biomarkers|March 29, 2020
A Novel Missense Variant in the ALX4 Gene Underlies Mild to Severe Frontonasal Dysplasia in a Consanguineous FamilyShabir Hussain, Umm-E-Kalsoom, Irfan Ullah, et al.IEEE Access : Practical Innovations, Open Solutions|November 23, 2021
Blockchain-Based Forward Supply Chain and Waste Management for COVID-19 Medical Equipment and SuppliesRaja Wasim Ahmad, Khaled Salah, Raja Jayaraman, et al.Cells|April 30, 2021
Dysregulation of Multiple Signaling Neurodevelopmental Pathways during Embryogenesis: A Possible Cause of Autism Spectrum DisorderJyoti Upadhyay, Jeevan Patra, Nidhi Tiwari, et al.Journal of Ayub Medical College, Abbottabad : JAMC|August 8, 2014
Risk factors for diabetic foot ulcerWasim Ahmad, Ishtiaq Ali Khan, Salma Ghaffar, et al.Journal of Chromatographic Science|August 28, 2013
HPLC and HPTLC methods by design for quantitative characterization and in vitro anti-oxidant activity of polyherbal formulation containing Rheum emodiWasim Ahmad, Syed Mohammad Arif Zaidi, Mohd Mujeeb, et al.Journal of AOAC International|February 11, 2022
Development and Validation of Ultra Performance Liquid Chromatography (UPLC) Method for the Quantitative Estimation of Caffeine in Non-Alcoholic Soft and Energy DrinksWasim Ahmad, Mohammad Yusuf, Ayaz Ahmad, et al.Cluster Computing|March 21, 2022
Blockchain for deep learning: review and open challengesMuhammad Shafay, Raja Wasim Ahmad, Khaled Salah, et al.Journal of Human Genetics|December 8, 2017
Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhinyAsmat Ullah, Muhammad Umair, Umm E-Kalsoom, et al.Human Genetics|December 12, 2007
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2Muhammad Jawad Hassan, Muhammad Salman Chishti, Syed Muhammad Jamal, et al.Pageof 242