(Q54694823)

2 June 2018

title

A novel PROP1 gene mutation (157delA) in Japanese siblings with combined anterior pituitary hormone deficiency. (English)

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2 June 2018

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Ke-Ita Tatsumi

1

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2 June 2018

Kiyoshi Kikuchi

series ordinal

2

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2 June 2018

Kumi Tsumura

series ordinal

3

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2 June 2018

Nobuyuki Amino

series ordinal

4

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2 June 2018

publication date

1 November 2004

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2 June 2018

published in

Clinical Endocrinology

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2 June 2018

volume

61

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2 June 2018

issue

5

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2 June 2018

page(s)

635-640

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2 June 2018

A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Planned caesarean section versus planned vaginal birth for breech presentation at term: a randomised multicentre trial. Term Breech Trial Collaborative Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

Human Prop-1: cloning, mapping, genomic structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02147.X

10.1111/J.1365-2265.2004.02147.X

21 January 2018

Identifiers

DOI

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2 June 2018

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2 June 2018