Etiology and treatment of hypogonadism in adolescents - Test2 - elhamkhani - TriplyDB

Etiology and treatment of hypogonadism in adolescents

Etiology and treatment of hypogonadism in adolescents

http://www.wikidata.org/entity/Q28265981

about

The study design and methodology for the ARCHER study--adolescent rural cohort study of hormones, health, education, environments and relationships.Male reprotoxicity and endocrine disruption.Puberty as a life history transition.

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Etiology and treatment of hypogonadism in adolescents

http://www.wikidata.org/entity/Q28265981

description

2009 nî lūn-bûn

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2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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type

label

Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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Etiology and treatment of hypogonadism in adolescents

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J.ECL.2009.08.004

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Endocrinology and Metabolism Clinics of North America

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Etiology and treatment of hypogonadism in adolescents

@en

P2093

Vidhya Viswanathan

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P2860

Synchronization of augmented luteinizing hormone secretion with sleep during puberty

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene

Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis

Five novel mutations in steroidogenic factor 1 (SF1, NR5A1) in 46,XY patients with severe underandrogenization but without adrenal insufficiency

Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia

Optimising management in Turner syndrome: from infancy to adult transfer

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719-38

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scholarly article

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10.1016/J.ECL.2009.08.004

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4

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38

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Erica A. Eugster

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2009-12-01T00:00:00Z

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40037434

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19944289

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4802969

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