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Page 1
Hypothalamic Reproductive Endocrine Pulse Generator Activity Independent of Neurokinin B and Dynorphin Signaling.
Lippincott MF, León S, Chan YM, Fergani C, Talbi R, Farooqi IS, Jones CM, Arlt W, Stewart SE, Cole TR, Terasawa E, Hall JE, Shaw ND, Navarro VM, Seminara SB. Lippincott MF, et al. Among authors: farooqi is. J Clin Endocrinol Metab. 2019 Oct 1;104(10):4304-4318. doi: 10.1210/jc.2019-00146. J Clin Endocrinol Metab. 2019. PMID: 31132118 Free PMC article.
Classification of Congenital Leptin Deficiency.
von Schnurbein J, Zorn S, Nunziata A, Brandt S, Moepps B, Funcke JB, Hussain K, Farooqi IS, Fischer-Posovszky P, Wabitsch M. von Schnurbein J, et al. Among authors: farooqi is. J Clin Endocrinol Metab. 2024 Sep 16;109(10):2602-2616. doi: 10.1210/clinem/dgae149. J Clin Endocrinol Metab. 2024. PMID: 38470203 Free PMC article.
FTO and obesity: the missing link.
Farooqi IS. Farooqi IS. Cell Metab. 2011 Jan 5;13(1):7-8. doi: 10.1016/j.cmet.2010.12.016. Cell Metab. 2011. PMID: 21195343 Free article.
Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction.
McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT. McCabe MJ, et al. Among authors: farooqi is. J Clin Endocrinol Metab. 2011 Oct;96(10):E1709-18. doi: 10.1210/jc.2011-0454. Epub 2011 Aug 10. J Clin Endocrinol Metab. 2011. PMID: 21832120 Free PMC article.
A novel mutation in the leptin gene (W121X) in an Egyptian family.
Mazen I, Amr K, Tantawy S, Farooqi IS, El Gammal M. Mazen I, et al. Among authors: farooqi is. Mol Genet Metab Rep. 2014 Nov 11;1:474-476. doi: 10.1016/j.ymgmr.2014.10.002. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896126 Free PMC article.
239 results