Muhammad M. Ajmal
Park Road
Islamabad, IS, Pakistan
Islamabad, IS, Pakistan
Last Updated: 09/26/2026
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Found 56 publications
Prevalence and clinical characteristics of probable familial chylomicronaemia syndrome at a tertiary care center in Pakistan: Insights from a hospital-based screening study.
Journal: Journal of clinical lipidology
Published: February 22, 2026
NLRP1 gene polymorphism rs2670660 is associated with vitiligo in the Pakistani population.
Journal: Molecular biology reports
Published: October 16, 2025
Prevalence of nutritional literacy and associated factors among adult residents: a cross-sectional study from marginalized Community in Islamabad, Pakistan.
Journal: Frontiers in public health
Published: September 03, 2025
Dyslipidaemia among children and adolescents in Pakistan: a five-year retrospective cohort study based on laboratory data.
Journal: Lipids in health and disease
Published: January 05, 2025
Trends and prevalence of severe hypertriglyceridemia in Pakistan: A 5-year analysis (2019-2023).
Journal: Journal of clinical lipidology
Published: November 07, 2024
Cascade screening of a Pakistani consanguineous familial hypercholesterolemia cohort: Identification of seven new homozygous patients.
Journal: Atherosclerosis
Published: October 04, 2024
Genetic and clinical characteristics of patients with lipoprotein lipase deficiency from Slovenia and Pakistan: case series and systematic literature review.
Journal: Frontiers in endocrinology
Published: February 17, 2024
Corrigendum: Targeted drug delivery systems: synthesis andin vitrobioactivity and apoptosis studies of gemcitabine-carbon dot conjugates (2020Biomed. Mater.15065004).
Journal: Biomedical materials (Bristol, England)
Published: May 02, 2023
Corrigendum: Development of biodegradable thin films for efficient, specific, and controlled delivery of capecitabine (2021Biomed. Mater.16 055019).
Journal: Biomedical materials (Bristol, England)
Published: April 24, 2023
Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family.
Journal: Medicina (Kaunas, Lithuania)
Published: December 07, 2022
KIF1A novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC.
Journal: The International journal of neuroscience
Published: October 25, 2022
Association of dopamine β-hydroxylase polymorphism rs1611115 and serum levels with psychiatric disorders in Pakistani population.
Journal: The International journal of neuroscience
Published: September 19, 2022
Last Updated: 09/26/2026