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Kallmann syndrome and hypogonadotrop...

Quinton, Richard.

Kallmann syndrome and hypogonadotropic hypogonadism

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Kallmann syndrome and hypogonadotropic hypogonadism/ volume editor, Richard Quinton.
other author:	Quinton, Richard.
Published:	Basel :S. Karger, : 2010,
Description:	1 online resource :ill. (some col.) :
Notes:	Genetics, developmental biology and clinical phenotypes
Subject:	Hypogonadism. -
Online resource:	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. - 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:

780588
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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245 0 0 $a Kallmann syndrome and hypogonadotropic hypogonadism $h [electronic resource] / $c volume editor, Richard Quinton.
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300 $a 1 online resource : $b ill. (some col.)
490 1 $a Frontiers of hormone research, $x 1662-3762 ; $v v. 39
500 $a Genetics, developmental biology and clinical phenotypes
504 $a Includes bibliographical references and indexes.
520 $a 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.
650 0 $a Hypogonadism. $3 780588
650 1 2 $a Hypogonadism $x genetics. $3 780888
650 1 2 $a Kallmann Syndrome $x genetics. $3 780889
700 1 $a Quinton, Richard. $3 780887
830 0 $a Frontiers of hormone research ; $v v. 37. $3 780587
856 4 0 $u http://content.karger.com/ProdukteDB/produkte.asp?Aktion=showproducts&searchWhat=books&searchParm=toc&ProduktNr=253826

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