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Saudi Medical Journal|December 7, 2017
Novel duplication mutation of the DYSF gene in a Pakistani family with Miyoshi MyopathyMuhammad I Ullah, Arsalan Ahmad, Milena Zarkovic, et al.
Recent Advances in Anti-Infective Drug Discovery|June 18, 2026
Antibiotic Resistance Patterns and Hospital-acquired Infection among COVID-19 Patients Attending Intensive Care Unit: A Single-center Descriptive StudyMuhammad Gulzada, Rukhsana Yasmeen, Komal Jamil, et al.
Molecules (Basel, Switzerland)|October 27, 2022
DAD-Net: Classification of Alzheimer's Disease Using ADASYN Oversampling Technique and Optimized Neural NetworkGulnaz Ahmed, Meng Joo Er, Mian Muhammad Sadiq Fareed, et al.
Indian Journal of Pediatrics|August 11, 2012
Molecular characterisation and prenatal diagnosis of Asparto-acylase deficiency (Canavan disease)--report of two novel and two known mutations from the Indian subcontinentSunita Bijarnia, Sudha Kohli, Ratna Dua Puri, et al.
Obesity Facts|July 30, 2019
Leptin Is Not Essential for Obesity-Associated HypertensionJulia von Schnurbein, Jaida Manzoor, Stephanie Brandt, et al.
Journal of Cardiac Surgery|March 28, 2022
Role of matrix metalloproteinases in mitral valve regurgitation: Association between the of MMP-1, MMP-9, TIMP-1, and TIMP-2 expression, degree of mitral valve insufficiency, and pathologic etiologyMarc Irqsusi, Azza Labene Mansouri, Anette Ramaswamy, et al.
Genes|March 25, 2022
Delineating Novel and Known Pathogenic Variants in <i>TYR</i>, <i>OCA2</i> and <i>HPS-1</i> Genes in Eight Oculocutaneous Albinism (OCA) Pakistani FamiliesMuhammad Shakil, Abida Akbar, Nazish Mahmood Aisha, et al.
Diabetes Care|January 26, 2018
Leptin Replacement Reestablishes Brain Insulin Action in the Hypothalamus in Congenital Leptin DeficiencySabine Frank-Podlech, Julia von Schnurbein, Ralf Veit, et al.
Eye (London, England)|April 19, 2019
Tyrosinase (TYR) gene sequencing and literature review reveals recurrent mutations and multiple population founder gene mutations as causative of oculocutaneous albinism (OCA) in Pakistani familiesMuhammad Shakil, Gaurav V Harlalka, Shamshad Ali, et al.
Neurogenetics|May 5, 2006
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM geneAsma Gul, Muhammad Jawad Hassan, Saqib Mahmood, et al.
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