Late-onset congenital central hypoventilation syndrome and a rare PHOX2B gene mutation-Reference-Cited by-同舟云学术

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Late-onset congenital central hypoventilation syndrome and a rare PHOX2B gene mutation

Published:2014-05-04 Issue:1 Volume:19 Page:55-60
ISSN:1520-9512
Container-title:Sleep and Breathing
language:en
Short-container-title:Sleep Breath

Author:

Magalhães Joana,Madureira Núria,Medeiros Rita,Fernandes Paula C.,Oufadem Myriam,Amiel Jeanne,Estêvão M. Helena,Reis M. Guilhermina

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s11325-014-0996-7.pdf

Reference26 articles.

1. Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Keens TG, Loghmanee DA, Trang H (2010) An official ATS clinical policy statement: congenital central hypoventilation syndrome—genetic basis, diagnosis, and management. Am J Respir Crit Care Med 181:626–644

2. Weese-Mayer DE, Rand CM, Berry-Kravis EM, Jennings LJ, Loghmanee DA, Patwari PP et al (2009) Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine. Pediatr Pulmonol 44:521–535

3. Trivedi A, Waters K, Suresh S, Nair R (2011) Congenital central hypoventilation syndrome: four families. Sleep Breath 15:785–789

4. Chen ML, Keens TG (2004) Congenital central hypoventilation syndrome: not just another rare disorder. Paediatr Respir Rev 5:182–189

5. Healy F, Marcus CL (2011) Congenital central hypoventilation syndrome in children. Paediatr Respir Rev 12:253–263

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5. Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndrome;Clinical Autonomic Research;2022-11-20

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