(Q31055358)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16918947%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

review article

1 reference

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16918947%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author

Luciani Renata Carvalho

3

1 reference

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29 December 2019

Mirian Yumie Nishi

5

1 reference

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29 December 2019

Angela S Barbosa

6

1 reference

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Berenice Bilharinho Mendonca

29 December 2019

9

1 reference

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29 December 2019

author name string

Abrão MG

1

1 reference

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29 December 2019

Leite MV

2

1 reference

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29 December 2019

Billerbeck AE

4

1 reference

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29 December 2019

Martin RM

7

1 reference

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29 December 2019

Arnhold IJ

8

1 reference

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29 December 2019

publication date

1 September 2006

1 reference

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29 December 2019

published in

Clinical Endocrinology

1 reference

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29 December 2019

volume

65

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29 December 2019

issue

3

1 reference

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29 December 2019

page(s)

294-300

1 reference

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Pituitary development: regulatory codes in mammalian organogenesis

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.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.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.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.1365-2265.2006.02592.X

Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.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.1365-2265.2006.02592.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.1365-2265.2006.02592.X

Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

MR imaging of the pituitary stalk: size, shape, and enhancement pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

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/10.1111%2FJ.1365-2265.2006.02592.X

Pseudotumor of the pituitary due to PROP-1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

Alu repeats and human genomic diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

Absent or delayed adrenarche in Pit-1/POU1F1 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

Human Prop-1: cloning, mapping, genomic structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02592.X

10.1111/J.1365-2265.2006.02592.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16918947%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference