Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

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Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

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http://www.wikidata.org/entity/Q48297715

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh

2015年學術文章

@zh-hant

name

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@en

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@nl

type

Item

label

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@en

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@nl

prefLabel

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@en

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@nl

P1476

Kallmann syndrome patient with gender dysphoria, multiple sclerosis, and thrombophilia.

@en

P2093

Andrew Davies

http://www.w3.org/2001/XMLSchema#string

Aniruthan Renukanthan

http://www.w3.org/2001/XMLSchema#string

Benjamin Turner

http://www.w3.org/2001/XMLSchema#string

Jane Evanson

http://www.w3.org/2001/XMLSchema#string

Leighton Seal

http://www.w3.org/2001/XMLSchema#string

Márta Korbonits

http://www.w3.org/2001/XMLSchema#string

Peter MacCallum

http://www.w3.org/2001/XMLSchema#string

Richard Green

http://www.w3.org/2001/XMLSchema#string

Richard Quinton

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P2860

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies

Endocrine treatment of transsexual persons: an Endocrine Society clinical practice guideline

Standards of Care for the Health of Transsexual, Transgender, and Gender-Nonconforming People, Version 7

Modelling genetic susceptibility to multiple sclerosis with family data.

Kallmann's syndrome: is it always for life?

Primary progressive multiple sclerosis: part of the MS disease spectrum or separate disease entity?

Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism.

Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system.

P2888

s12020-015-0562-5

P304

496-503

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P31

scholarly article

P356

10.1007/S12020-015-0562-5

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Márta Korbonits

P577

2015-03-05T00:00:00Z

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P5875

273149780

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P698

25739677

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P921

thrombophilia

multiple sclerosis