(Q39163940)

English

PROP-1 Gene Mutation (R120C) Causing Combined Pituitary Hormone Deficiencies with Variable Clinical Course in Eight Siblings of One Jewish Moroccan Family

scientific article published on January 1, 2003

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Europe PubMed Central

PubMed publication ID

9 September 2017

PROP-1 gene mutation (R120C) causing combined pituitary hormone deficiencies with variable clinical course in eight siblings of one Jewish Moroccan family (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

PROP-1 Gene Mutation (R120C) Causing Combined Pituitary Hormone Deficiencies with Variable Clinical Course in Eight Siblings of One Jewish Moroccan Family (English)

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

1 reference

based on heuristic

inferred from title

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

author name string

L. Lazar

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14614227

1 April 2024

G. Gat-Yablonski

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14614227

1 April 2024

L. Kornreich

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14614227

1 April 2024

A. Pertzelan

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14614227

1 April 2024

M. Phillip

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14614227

1 April 2024

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publication date

1 January 2003

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

full work available at URL

https://www.karger.com/Article/Pdf/74036

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Hormone Research

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

60

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

227-231

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

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

1

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Establishment of reference values for standard dose short synacthen test (250 microgram), low dose short synacthen test (1 microgram) and insulin tolerance test for assessment of the hypothalamo-pituitary-adrenal axis in normal subjects

3

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Sequence-Determined DNA Separations

4

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Mutations in PROP1 cause familial combined pituitary hormone deficiency

5

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

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)

6

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects

7

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

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

8

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

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

9

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

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

10

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

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

11

1 reference

10.1159/000074036

https://api.crossref.org/works/10.1159/000074036

1 April 2024

Identifiers

10.1159/000074036

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

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