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Loss-of-function mutations in ADCY3 cause monogenic severe obesity.
Saeed S, Bonnefond A, Tamanini F, Mirza MU, Manzoor J, Janjua QM, Din SM, Gaitan J, Milochau A, Durand E, Vaillant E, Haseeb A, De Graeve F, Rabearivelo I, Sand O, Queniat G, Boutry R, Schott DA, Ayesha H, Ali M, Khan WI, Butt TA, Rinne T, Stumpel C, Abderrahmani A, Lang J, Arslan M, Froguel P. Saeed S, et al. Among authors: butt ta. Nat Genet. 2018 Feb;50(2):175-179. doi: 10.1038/s41588-017-0023-6. Epub 2018 Jan 8. Nat Genet. 2018. PMID: 29311637 Free article.
Genetic Causes of Severe Childhood Obesity: A Remarkably High Prevalence in an Inbred Population of Pakistan.
Saeed S, Arslan M, Manzoor J, Din SM, Janjua QM, Ayesha H, Ain QT, Inam L, Lobbens S, Vaillant E, Durand E, Derhourhi M, Amanzougarene S, Badreddine A, Berberian L, Gaget S, Khan WI, Butt TA, Bonnefond A, Froguel P. Saeed S, et al. Among authors: butt ta. Diabetes. 2020 Jul;69(7):1424-1438. doi: 10.2337/db19-1238. Epub 2020 Apr 29. Diabetes. 2020. PMID: 32349990
High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptor.
Saeed S, Khanam R, Janjua QM, Manzoor J, Ning L, Hanook S, Canouil M, Ali M, Ayesha H, Khan WI, Farooqi IS, Yeo GSH, O'Rahilly S, Bonnefond A, Butt TA, Arslan M, Froguel P. Saeed S, et al. Among authors: butt ta. Cell Rep Med. 2023 Sep 19;4(9):101187. doi: 10.1016/j.xcrm.2023.101187. Epub 2023 Sep 1. Cell Rep Med. 2023. PMID: 37659411 Free PMC article.
A 7-month-old infant with Cushing's disease.
Abbas R, Hamid MH, Sarwar M, Butt TA, Qureshi A, Malik N. Abbas R, et al. Among authors: butt ta. J Coll Physicians Surg Pak. 2013 Aug;23(8):596-7. J Coll Physicians Surg Pak. 2013. PMID: 23930882
A neonate with Poland-Mobius syndrome.
Abbas R, Qureshi AU, Ahmad TM, Butt TA. Abbas R, et al. Among authors: butt ta. J Coll Physicians Surg Pak. 2011 Oct;21(10):640-1. doi: 10.2011/JCPSP.640641. J Coll Physicians Surg Pak. 2011. PMID: 22015131
24 results