(Q50459589)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17223984%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

title

Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17223984%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference

Ana Claudia Latronico Xavier

7

1 reference

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24 December 2019

Marcel Koenigkam-Santos

3

1 reference

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24 December 2019

Lucila L. Elias

5

1 reference

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24 December 2019

Margaret de Castro

8

1 reference

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24 December 2019

author name string

Beatriz R Versiani

1

1 reference

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24 December 2019

Ericka Trarbach

2

1 reference

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24 December 2019

Antonio Carlos Dos Santos

4

1 reference

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24 December 2019

Ayrton C Moreira

6

1 reference

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24 December 2019

publication date

1 February 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17223984%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

published in

Clinical Endocrinology

1 reference

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24 December 2019

volume

66

1 reference

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24 December 2019

issue

2

1 reference

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24 December 2019

page(s)

173-179

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17223984%20AND%20SRC:MED&resulttype=core&format=json

Genetics of human hypogonadotropic hypogonadism

24 December 2019

cites work

1 reference

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Advances in the molecular genetics of hypogonadotropic hypogonadism

21 January 2018

1 reference

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Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization.

21 January 2018

1 reference

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GnRH neuronal development: insights into hypogonadotrophic hypogonadism

21 January 2018

1 reference

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A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor

21 January 2018

1 reference

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Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Mutations of the GnRH receptor gene: a new cause of autosomal-recessive hypogonadotropic hypogonadism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

A novel homozygous mutation in the second transmembrane domain of the gonadotrophin releasing hormone receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

21 January 2018

1 reference

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X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene

21 January 2018

1 reference

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The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

21 January 2018

1 reference

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Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

FGF signaling through FGFR1 is required for olfactory bulb morphogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Kallmann syndrome: fibroblast growth factor signaling insufficiency?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

21 January 2018

1 reference

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Development of the University of Pennsylvania Smell Identification Test: a standardized microencapsulated test of olfactory function.

21 January 2018

1 reference

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Mirror movements in X-linked Kallmann's syndrome. I. A neurophysiological study

21 January 2018

1 reference

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A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome.

21 January 2018

1 reference

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Autosomal recessive idiopathic hypogonadotropic hypogonadism: genetic analysis excludes mutations in the gonadotropin-releasing hormone (GnRH) and GnRH receptor genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Abnormal development of the olfactory bulb and reproductive system in mice lacking prokineticin receptor PKR2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

The Kallmann's syndrome variant (KSV) model of the schizophrenias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X

Two Novel Mutations in the Gonadotropin-Releasing Hormone Receptor Gene in Brazilian Patients with Hypogonadotropic Hypogonadism and Normal Olfaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02702.X