(Q31035731)

28 June 2017

title

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

1 reference

growth hormone deficiency

28 June 2017

main subject

1 reference

1 reference

3

0 references

author name string

Dominique Simon

1

1 reference

28 June 2017

Charalambos Hadjiathanasiou

2

1 reference

28 June 2017

Paul Czernichow

4

1 reference

28 June 2017

Juliane Léger

5

1 reference

28 June 2017

publication date

1 April 2006

1 reference

28 June 2017

published in

Clinical Endocrinology

1 reference

28 June 2017

volume

64

1 reference

28 June 2017

issue

4

1 reference

28 June 2017

page(s)

416-422

1 reference

Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function

28 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Midline brain lesions in children with hormone insufficiency indicate early prenatal damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Transcription factors in pituitary gland development and their clinical impact on phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.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.1365-2265.2006.02484.X

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.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.1365-2265.2006.02484.X

Endocrinopathies associated with midline cerebral and cranial malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Auxological, ophthalmological, neurological and MRI findings in 25 Austrian patients with septo-optic dysplasia (SOD). Preliminary data

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Growth hormone deficiency caused by pituitary stalk interruption in Fanconi's anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Long-term treatment with growth hormone improves final height in a patient with Pallister-Hall syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

A patient with de Morsier and Duane syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Autosomal dominant sacral agenesis: Currarino syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

SOX3 is required during the formation of the hypothalamo-pituitary axis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Pallister-Hall syndrome phenotype in mice mutant for Gli3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Multiple hits during early embryonic development: digenic diseases and holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Molecular basis of environmentally induced birth defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Speculations on the pathogenesis of CHARGE syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part II: Neuropathological considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02484.X

10.1111/J.1365-2265.2006.02484.X

21 January 2018

Identifiers

DOI

1 reference

28 June 2017

1 reference