(Q47332580)

14 January 2018

title

Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism? (English)

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14 January 2018

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3

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author name string

A Voutetakis

1

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14 January 2018

A Sertedaki

2

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14 January 2018

P Xekouki

4

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14 January 2018

I Bossis

5

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14 January 2018

C Dacou-Voutetakis

6

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14 January 2018

M I Argyropoulou

7

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14 January 2018

publication date

1 May 2006

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14 January 2018

Journal of Endocrinological Investigation

published in

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14 January 2018

volume

29

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14 January 2018

issue

5

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14 January 2018

page(s)

462-466

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14 January 2018

https://scigraph.springernature.com/pub.10.1007/bf03344131

exact match

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cites work

Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Pituitary development: regulatory codes in mammalian organogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Molecular basis of combined pituitary hormone deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Height of normal pituitary gland as a function of age evaluated by magnetic resonance imaging in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Familial Hypopituitarism with Large Sella Turcica

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03344131

Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia

21 January 2018

1 reference

12 December 2020

MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

Heritable disorders of pituitary development

1 reference

12 December 2020

Role of PROP1 in Pituitary Gland Growth

1 reference

12 December 2020

Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C)

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03344131

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14 January 2018

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14 January 2018