(Q55982676)

Steve Cunningham

7

0 references

Sophie Caillat-Zucman

Sophie Caillat-Zucman

3

0 references

Yanick J. Crow

Yanick Crow

6

0 references

Stanislas Lyonnet

Stanislas Lyonnet

17

0 references

Loic de Pontual

Loic De Pontual

1

0 references

Jeanne Amiel

Jeanne Amiel

19

0 references

Arnold Munnich

16

Arnold Munnich

0 references

Pierre Bougnères

5

Pierre Bougneres

0 references

author name string

Othman A Abou Shenab

4

0 references

Blandine Esteva

8

0 references

Lada Cindro Heberle

9

0 references

Juliane Leger

10

0 references

Graziella Pinto

11

0 references

Michel Polak

12

0 references

Magdy Helmy Shafik

13

0 references

Christian Straus

14

0 references

Ha Trang

15

0 references

Isabelle Desguerre

Congenital central hypoventilation syndrome: an update

18

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language of work or name

English

0 references

publication date

December 2008

0 references

published in

Pediatric Research

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volume

64

0 references

issue

6

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page(s)

689-694

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cites work

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Regulation of respiration (first of three parts).

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

PHOX2B gene mutation in a patient with late-onset central hypoventilation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Late-onset central hypoventilation with hypothalamic dysfunction: a distinct clinical syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Body mass index and hypothalamic morphology on MRI in children with congenital midline cerebral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Molecular genetic defects in congenital hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Autonomic function in children with congenital central hypoventilation syndrome and their families

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Idiopathic hypothalamic dysfunction with dilated unresponsive pupils: report of two cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Opsoclonus myoclonus syndrome in neuroblastoma a report from a workshop on the dancing eyes syndrome at the advances in neuroblastoma meeting in Genoa, Italy, 2004.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Mash1 is required for generic and subtype differentiation of hypothalamic neuroendocrine cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E

Idiopathic hypothalamic dysfunction: a paraneoplastic syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E318187DD0E