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Kallmann syndrome and hypogonadotrop...
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Quinton, Richard.
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Kallmann syndrome and hypogonadotropic hypogonadism
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Kallmann syndrome and hypogonadotropic hypogonadism/ volume editor, Richard Quinton.{me_controlnum}
其他作者:
Quinton, Richard.
出版者:
Basel :S. Karger, : 2010,
面頁冊數:
1 online resource :ill. (some col.)
附註:
Genetics, developmental biology and clinical phenotypes
標題:
Hypogonadism. -
電子資源:
http://content.karger.com/ProdukteDB/produkte.asp?Aktion=showproducts&searchWhat=books&searchParm=toc&ProduktNr=253826
ISBN:
9783805586184
Kallmann syndrome and hypogonadotropic hypogonadism
Kallmann syndrome and hypogonadotropic hypogonadism
[electronic resource] /volume editor, Richard Quinton.{me_controlnum} - Basel :S. Karger,2010 - 1 online resource :ill. (some col.) - Frontiers of hormone research,v. 391662-3762 ;. - Frontiers of hormone research ;v. 37..
Genetics, developmental biology and clinical phenotypes
Includes bibliographical references and indexes.
Over the past decade, the understanding of the processes involved in the regulation of gonadotropin-releasing hormone and its dysfunction has greatly increased. As new regulatory peptides have been identified, the underlying causes of central hypogonadism have multiplied, and the area has become increasingly complex. The reversibility of even genetically determined hypogonadotropic hypogonadism has become more firmly established, and clinical studies have greatly expanded our understanding of basic physiological pathways. Structuring this mass of new knowledge in thirteen comprehensive chapters, a group of renowned experts, representing the principal international research groups, take stock of the most recent progress.This up-to-date overview helps scientists and clinicians to plan future research and treat patients with delayed puberty, hypogonadotropic hypogonadism and other forms of central reproductive disorders.
ISBN: 9783805586184Subjects--Topical Terms:
1360629
Hypogonadism.
LC Class. No.: RC898 / .K35 2010
Dewey Class. No.: 616.4/7
National Library of Medicine Call No.: W1 / FR946F v.39 2010
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