Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome. (Q36576987)

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29 December 2019

review article

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title

Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome (English)

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29 December 2019

1

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29 December 2019

author name string

John C Gill

series ordinal

2

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29 December 2019

publication date

1 March 2006

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Nature Clinical Practice Endocrinology and Metabolism

29 December 2019

published in

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29 December 2019

volume

2

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29 December 2019

page(s)

160-171

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issue

3

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Gonadotropin-releasing hormone deficiency in men: diagnosis and treatment with exogenous gonadotropin-releasing hormone

29 December 2019

cites work

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Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene

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Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene.

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Kallmann syndrome: towards molecular pathogenesis

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Hypogonadotropic disorders in men and women: diagnosis and therapy with pulsatile gonadotropin-releasing hormone

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Successful GnRH treatment in a patient with Kallmann's syndrome, who previously failed HMG/HCG treatment

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Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons.

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Ontogeny of GnRH and olfactory neuronal systems in man: novel insights from the investigation of inherited forms of Kallmann's syndrome.

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X chromosome-linked Kallmann syndrome: clinical heterogeneity in three siblings carrying an intragenic deletion of the KAL-1 gene.

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7 January 2021

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7 January 2021

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7 January 2021

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Olfactory structures in staged human embryos

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7 January 2021

Identifiers

DOI

10.1038/NCPENDMET0119

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16932275%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

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