Taeed A. Butt
Lahore, PB, Pakistan
Last Updated: 09/26/2026
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Found 9 publications
A National Survey on Congenital Hypothyroidism Newborn Screening in Pakistan.
Journal: Global pediatric health
Published: May 03, 2024
High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor.
Journal: Cell reports. Medicine
Published: March 21, 2023
Loss-of-function mutations in ADCY3 cause monogenic severe obesity.
Journal: Nature genetics
Published: April 30, 2017
Erratum: Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population.
Journal: Obesity (Silver Spring, Md.)
Published: March 29, 2017
Iatrogenic Cushing's syndrome in children presenting at Children's Hospital Lahore using nappy rash ointments.
Journal: JPMA. The Journal of the Pakistan Medical Association
Published: June 02, 2015
Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population.
Journal: Obesity (Silver Spring, Md.)
Published: February 20, 2015
Novel LEPR mutations in obese Pakistani children identified by PCR-based enrichment and next generation sequencing.
Journal: Obesity (Silver Spring, Md.)
Published: October 09, 2013
High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families.
Journal: Molecular genetics and metabolism
Published: February 06, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026