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JMIR Medical Education|February 21, 2024
Evaluating Large Language Models for the National Premedical Exam in India: Comparative Analysis of GPT-3.5, GPT-4, and BardFaiza Farhat, Beenish Moalla Chaudhry, Mohammad Nadeem, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|September 12, 2024
Effect of Gender on Metabolic and Neurodevelopmental Parameters of Postnatally Growth-Restricted Rats Undergoing Catch-Up GrowthFaiza Ikram, Muhammad Ali Rabani, Sidra Arshad, et al.
Food Science and Biotechnology|March 2, 2026
Preparation of Korean rice wine with probiotic indigenous Saccharomyces cerevisiae and their fermentation propertiesFaiza Khalid, Hao Jin, Eun-Gyo Lee, et al.
Behavioural Pharmacology|July 18, 2023
Liver tryptophan 2,3-dioxygenase: a determinant of anxiety-like behaviour - studies with chronic nicotine administration in ratsSamina Bano, Humaira Sharif, Faiza Sajid, et al.
Frontiers in Microbiology|June 12, 2023
Antimicrobial resistance and machine learning: past, present, and futureFaiza Farhat, Md Tanwir Athar, Sultan Ahmad, et al.
Nutrients|January 16, 2021
Alternate Day Fasting Combined with a Low Carbohydrate Diet: Effect on Sleep Quality, Duration, Insomnia Severity and Risk of Obstructive Sleep Apnea in Adults with ObesityFaiza Kalam, Kelsey Gabel, Sofia Cienfuegos, et al.
World Journal of Emergency Surgery : WJES|November 11, 2008
Spectrum of perforation peritonitis in Pakistan: 300 cases Eastern experienceShahida Parveen Afridi, Faiza Malik, Shafiq Ur-Rahman, et al.
Journal of Human Genetics|December 14, 2011
CAPN3 mRNA processing alteration caused by splicing mutation associated with novel genomic rearrangement of Alu elementsIkhlass Hadj Salem, Ines Hsairi, Najla Mezghani, et al.
Bone|December 28, 2010
Matrix metalloproteinases in osteoclasts of ontogenetic and regenerating zebrafish scalesErik de Vrieze, Faiza Sharif, Juriaan R Metz, et al.
Journal of Child Neurology|June 8, 2010
Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III geneEmna Mkaouar-Rebai, Emna Ellouze, Imen Chamkha, et al.
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