Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death-Reference-Cited by-同舟云学术

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Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death

Published:2012-09 Issue:1-2 Volume:170 Page:12-19
ISSN:1566-0702
Container-title:Autonomic Neuroscience
language:en
Short-container-title:Autonomic Neuroscience

Author:

Lavezzi Anna M.,Weese-Mayer Debra E.,Yu Margaret Y.,Jennings Lawrence J.,Corna Melissa F.,Casale Valentina,Oneda Roberta,Matturri Luigi

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Endocrine and Autonomic Systems

Reference44 articles.

1. Photostimulation of retrotrapezoid nucleus phox2b-expressing neurons in vivo produces long-lasting activation of breathing in rats;Abbott;J. Neurosci.,2009

2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in Congenital Central Hypoventilation Syndrome;Amiel;Nat. Genet.,2003

3. A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea and specific loss of parafacial neurons;Dubreuil;Proc. Natl. Acad. Sci. U. S. A.,2008

4. Breathing with phox2b;Dubreuil;Philos. Trans. R. Soc. Lond. B Biol. Sci.,2009

5. Breathing: rhythmicity, plasticity, chemosensitivity;Feldman;Annu. Rev. Neurosci.,2003

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4. Evidence Base for 2022 Updated Recommendations for a Safe Infant Sleeping Environment to Reduce the Risk of Sleep-Related Infant Deaths;Pediatrics;2022-06-21

5. Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death;PLOS ONE;2022-04-29

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