(Q48935688)

17 February 2018

title

Case seminar: a young female with acute hyponatremia and a sellar mass. (English)

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17 February 2018

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4

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17 February 2018

Anne Barlier

6

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17 February 2018

Thierry Brue

7

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17 February 2018

author name string

Sandra Pekic

1

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17 February 2018

Mirjana Doknic

2

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17 February 2018

Dragana Miljic

3

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17 February 2018

Rachel Reynaud

5

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17 February 2018

Vera Popovic

8

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17 February 2018

publication date

24 August 2011

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17 February 2018

published in

Endocrine

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17 February 2018

volume

40

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17 February 2018

issue

3

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17 February 2018

page(s)

325-331

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17 February 2018

https://scigraph.springernature.com/pub.10.1007/s12020-011-9516-8

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Genetic regulation of the embryology of the pituitary gland and somatotrophs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

The molecular basis for developmental disorders of the pituitary gland in man.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

The spectrum of hypopituitarism caused by PROP1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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%2FS12020-011-9516-8

GH deficiency might be associated with normal height in PROP1 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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/10.1007%2FS12020-011-9516-8

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/10.1007%2FS12020-011-9516-8

Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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%2FS12020-011-9516-8

Prop-1 gene expression in human pituitary tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Pituitary tumours: inflammatory and granulomatous expansive lesions of the pituitary

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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%2FS12020-011-9516-8

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Familial Hypopituitarism with Large Sella Turcica

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

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/10.1007%2FS12020-011-9516-8

Pituitary enlargement in patients with PROP1 gene inactivating mutation represents cystic hyperplasia of the intermediate pituitary lobe. Histopathology and over 10 years follow-up of two patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Disorders of water and salt metabolism associated with pituitary disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Hyponatremia treatment guidelines 2007: expert panel recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

A syndrome of renal sodium loss and hyponatremia probably resulting from inappropriate secretion of antidiuretic hormone

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Osmotic demyelination syndrome following correction of hyponatremia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

Hyponatremia: endocrinologic causes and consequences of therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

DDAVP is effective in preventing and reversing inadvertent overcorrection of hyponatremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12020-011-9516-8

A Familial Form of Congenital Hypopituitarism Due to aPROP1Mutation in a Large Kindred: Phenotypic andin VitroFunctional Studies

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

An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain

1 reference

12 December 2020

Multiple pituitary hormone deficiency (MPHD) associated with normal height, absent puberty and obesity.

1 reference

12 December 2020

Heritable disorders of pituitary development

1 reference

12 December 2020

The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency

1 reference

12 December 2020

Role of PROP1 in Pituitary Gland Growth

1 reference

12 December 2020

Role of plasma arginine vasopressin in the impaired water diuresis of isolated glucocorticoid deficiency in the rat

1 reference

12 December 2020

Hyponatremia and inappropriate secretion of vasopressin (antidiuretic hormone) in patients with hypopituitarism

1 reference

12 December 2020

Pseudotumor of the pituitary due to PROP-1 deletion

1 reference

12 December 2020

10.1007/S12020-011-9516-8

Identifiers

DOI

1 reference

17 February 2018

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17 February 2018