(Q43943023)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

0 references

Dominique Bremond-Gignac

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

3

Clarisse Baumann

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

author name string

Sophie Guilmin-Crépon

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Catherine Garel

2

1 reference

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29 December 2019

Isabelle Bailleul-Forestier

5

1 reference

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29 December 2019

Suzel Magnier

6

1 reference

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29 December 2019

Mireille Castanet

7

1 reference

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29 December 2019

Paul Czernichow

8

1 reference

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29 December 2019

Thierry VAN DEN Abbeele

9

1 reference

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29 December 2019

Juliane Léger

10

1 reference

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29 December 2019

language of work or name

English

0 references

publication date

28 August 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

60

1 reference

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29 December 2019

issue

4

1 reference

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29 December 2019

page(s)

478-484

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

Congenital nasal stenosis in newborn infants

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Congenital nasal pyriform aperture stenosis: diagnosis and management of 20 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Congenital nasal pyriform aperture stenosis: diagnosis and treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Congenital nasal pyriform aperture stenosis. Isolated abnormality vs developmental field defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Nasal pyriform aperture stenosis and the holoprosencephaly spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Congenital nasal pyriform aperture stenosis with semilobar holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Nasal pyriform aperture stenosis and absence of the anterior pituitary gland: report of two cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Pituitary dysfunction, morbidity and mortality with congenital midline malformation of the cerebrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

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/10.1203%2F01.PDR.0000238380.03683.CB

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Optic nerve hypoplasia. Clinical significance of associated central nervous system abnormalities on magnetic resonance imaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Magnetic resonance diagnosis of congenital hypopituitarism in children with optic nerve hypoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Endocrinopathies associated with midline cerebral and cranial malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Endocrine status in patients with optic nerve hypoplasia: relationship to midline central nervous system abnormalities and appearance of the hypothalamic-pituitary axis on magnetic resonance imaging.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Do all patients with childhood-onset growth hormone deficiency (GHD) and ectopic neurohypophysis have persistent GHD in adulthood?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Anatomical consideration of the congenital nasal pyriform aperture stenosis: localized dysostosis without interorbital hypoplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Choanal atresia and associated multiple anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Multiple hits during early embryonic development: digenic diseases and holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Molecular basis of environmentally induced birth defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Speculations on the pathogenesis of CHARGE syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

CHARGE syndrome includes hypogonadotropic hypogonadism and abnormal olfactory bulb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

Perspective: genetic and genomic approaches in elucidating mechanisms of pituitary development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F01.PDR.0000238380.03683.CB

10.1203/01.PDR.0000238380.03683.CB

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16940234%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 December 2019

1051477573

0 references

1 reference