Neurocognitive monitoring in congenital central hypoventilation syndrome with the NIH Toolbox®

Congenital central hypoventilation syndrome (CCHS) is a rare neurocristopathy, caused by mutations in the paired‐like homeobox gene PHOX2B, which alters control of breathing and autonomic nervous system regulation, necessitating artificial ventilation as life‐support. A broad range of neurocognitive...

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Detalles Bibliográficos
Autores principales: Welbel, Remi Z., Rand, Casey M., Zhou, Amy, Fadl‐Alla, Allaa, Chen, Maida Lynn, Weese‐Mayer, Debra E., Zelko, Frank A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541049/
https://www.ncbi.nlm.nih.gov/pubmed/35574731
http://dx.doi.org/10.1002/ppul.25973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541049/
https://www.ncbi.nlm.nih.gov/pubmed/35574731
http://dx.doi.org/10.1002/ppul.25973

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