Human GnRH Deficiency: A Unique Disease Model to Unravel the Ontogeny of GnRH Neurons-Reference-Cited by-同舟云学术

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Human GnRH Deficiency: A Unique Disease Model to Unravel the Ontogeny of GnRH Neurons

Published:2010 Issue:2 Volume:92 Page:81-99
ISSN:1423-0194
Container-title:Neuroendocrinology
language:en
Short-container-title:Neuroendocrinology

Author:

Balasubramanian Ravikumar,Dwyer Andrew,Seminara Stephanie B.,Pitteloud Nelly,Kaiser Ursula B.,Crowley, Jr. William F.

Publisher

S. Karger AG

Subject

Cellular and Molecular Neuroscience,Endocrine and Autonomic Systems,Endocrinology,Endocrinology, Diabetes and Metabolism

Cited by 76 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Variety of genetic defects in GnRH and hypothalamic–pituitary signaling and development in normosmic patients with IHH;Frontiers in Endocrinology;2024-07-01

2. Endocrine Genetic Defects;Reference Module in Biomedical Sciences;2024

3. AXL receptor tyrosine kinase modulates gonadotropin-releasing hormone receptor signaling;Cell Communication and Signaling;2023-10-12

4. Treatment of congenital hypogonadotropic hypogonadism in male patients;Annals of Pediatric Endocrinology & Metabolism;2022-09-30

5. Hypogonadism in Males With Genetic Neurodevelopmental Syndromes;The Journal of Clinical Endocrinology & Metabolism;2022-08-01

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