Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Cancers|August 26, 2023
Long-Term Survival Analysis and Prognostic Factors of Arabic Patients with Differentiated Thyroid Carcinoma: A 20-Year Observational Study at the King Hussein Cancer Center (KHCC) Involving 528 PatientsAkram Al-Ibraheem, Ula Al-Rasheed, Noor Mashhadani, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Genetic overlap in Kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasiaTaneli Raivio, Magdalena Avbelj, Mark J McCabe, et al.
Human Molecular Genetics|July 10, 2012
An ancient founder mutation in PROKR2 impairs human reproductionMagdalena Avbelj Stefanija, Marc Jeanpierre, Gerasimos P Sykiotis, et al.
EMBO Molecular Medicine|July 30, 2017
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismCheng Xu, Andrea Messina, Emmanuel Somm, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 14, 2014
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutationsCarine Villanueva, Elka Jacobson-Dickman, Cheng Xu, et al.
Redox Biology|March 9, 2025
Health position paper and redox perspectives - Bench to bedside transition for pharmacological regulation of NRF2 in noncommunicable diseasesAntonio Cuadrado, Eduardo Cazalla, Anders Bach, et al.
American Journal of Human Genetics|May 7, 2013
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadismHichem Miraoui, Andrew A Dwyer, Gerasimos P Sykiotis, et al.
European Journal of Endocrinology|February 9, 2018
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architecturesDaniele Cassatella, Sasha R Howard, James S Acierno, et al.
Pageof 10