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JPMA. the Journal of the Pakistan Medical Association|February 26, 2023
Antecedent infections, recent developments and future directions in Guillain-Barré syndromeRashid Iqbal, Muhammad Javaid Asad, Raja Tahir Mahmood, et al.
Arthritis Research & Therapy|August 24, 2013
Association of HLA-DRB1 and -DQB1alleles and haplotypes with rheumatoid arthritis in a Pakistani populationAmbreen Gul Muazzam, Atika Mansoor, Lubna Ali, et al.
JPMA. the Journal of the Pakistan Medical Association|November 16, 2021
Study of Guillain-Barre syndrome etiology in Pakistani patientsRashid Iqbal, Muhammad Javaid Asad, Saima Siddiqi, et al.
Journal of Human Genetics|October 10, 2014
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani familySaima Siddiqi, Muhammad Ismail, Jaap Oostrik, et al.
Genetic Vaccines and Therapy|September 7, 2011
Occult HCV or delayed viral clearance from lymphocytes of Chronic HCV genotype 3 patients after interferon therapyAmbreen G Muazzam, Saleem Qureshi, Atika Mansoor, et al.
The Journal of General Virology|April 16, 2010
Patient HLA-DRB1* and -DQB1* allele and haplotype association with hepatitis C virus persistence and clearanceLubna Ali, Atika Mansoor, Nafees Ahmad, et al.
Iranian Journal of Pharmaceutical Research : IJPR|September 19, 2019
Genetic Polymorphism of CYP2C19 in Pakistani PopulationSana Riaz, Sadia Muhammad Din, Muhammad Usman Tareen, et al.
Journal of Biomolecular Structure & Dynamics|October 14, 2025
Novel Filamin genes variants implicated in skeletal dysplasias: integrated structural modeling and in silico functional characterizationMaha Yousaf, Ayesha Zaka, Shaheen Shahzad, et al.
Journal of Biomedical Science|April 30, 2019
Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis ImperfectaMehran Kausar, Saima Siddiqi, Muhammad Yaqoob, et al.
Journal of Biomedical Science|November 19, 2018
Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis ImperfectaMehran Kausar, Saima Siddiqi, Muhammad Yaqoob, et al.
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