GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature-Reference-Cited by-同舟云学术

GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature

Published:2020-08-28 Issue: Volume:11 Page:
ISSN:1664-2392
Container-title:Frontiers in Endocrinology
language:
Short-container-title:Front. Endocrinol.

Author:

Neocleous Vassos,Fanis Pavlos,Toumba Meropi,Tanteles George A.,Schiza Melpo,Cinarli Feride,Nicolaides Nicolas C.,Oulas Anastasis,Spyrou George M.,Mantzoros Christos S.,Vlachakis Dimitrios,Skordis Nicos,Phylactou Leonidas A.

Publisher

Frontiers Media SA

Subject

Endocrinology, Diabetes and Metabolism

Reference144 articles.

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4. Recombinant LH (lutropin alfa) for the treatment of hypogonadotrophic women with profound LH deficiency: a randomized, double-blind, placebo-controlled, proof-of-efficacy study;Shoham;Clin Endocrinol (Oxf).,2008

5. Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations;Seminara;Endocr Rev.,1998

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