(Q80385487)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526936%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526936%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

Zita Halász

1

1 reference

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31 December 2019

Judit Toke

2

1 reference

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31 December 2019

Attila Patócs

3

1 reference

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31 December 2019

Rita Bertalan

4

1 reference

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31 December 2019

Zsófia Tömböl

5

1 reference

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31 December 2019

Agnes Sallai

6

1 reference

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31 December 2019

Eva Hosszú

7

1 reference

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31 December 2019

Agota Muzsnai

8

1 reference

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31 December 2019

László Kovács

9

1 reference

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31 December 2019

János Sólyom

10

1 reference

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31 December 2019

György Fekete

11

1 reference

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31 December 2019

Károly Rácz

12

1 reference

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31 December 2019

publication date

1 December 2006

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31 December 2019

1 reference

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31 December 2019

volume

30

1 reference

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31 December 2019

issue

3

1 reference

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31 December 2019

page(s)

255-260

1 reference

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https://scigraph.springernature.com/pub.10.1007/s12020-006-0002-7

31 December 2019

exact match

0 references

cites work

Molecular basis of combined pituitary hormone deficiencies

1 reference

12 December 2020

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

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

The spectrum of hypopituitarism caused by PROP1 mutations

1 reference

12 December 2020

Molecular analysis of LHX3 and PROP-1 in pituitary hormone deficiency patients with posterior pituitary ectopia

1 reference

12 December 2020

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.

1 reference

12 December 2020

Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates

1 reference

12 December 2020

Genetic regulation of the embryology of the pituitary gland and somatotrophs

1 reference

12 December 2020

Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic defects in the development and function of the anterior pituitary gland

1 reference

12 December 2020

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

1 reference

12 December 2020

The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia

1 reference

12 December 2020

Role of PROP1 in Pituitary Gland Growth

1 reference

12 December 2020

Mutations in PROP1 cause familial combined pituitary hormone deficiency

1 reference

12 December 2020

Diagnosis of growth hormone deficiency in adults

1 reference

12 December 2020

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

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

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency

1 reference

12 December 2020

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Untreated hypopituitarism due to absence of the pituitary stalk with normal adult height: report of two cases

1 reference

12 December 2020

The Ames dwarf gene is required for Pit-1 gene activation.

1 reference

12 December 2020

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

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

Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects.

1 reference

12 December 2020

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

1 reference

12 December 2020

Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X).

1 reference

12 December 2020

10.1007/S12020-006-0002-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526936%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference