These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
420 related articles for article (PubMed ID: 19422034)
1. Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine. Weese-Mayer DE; Rand CM; Berry-Kravis EM; Jennings LJ; Loghmanee DA; Patwari PP; Ceccherini I Pediatr Pulmonol; 2009 Jun; 44(6):521-35. PubMed ID: 19422034 [TBL] [Abstract][Full Text] [Related]
2. Pupillometry in congenital central hypoventilation syndrome (CCHS): quantitative evidence of autonomic nervous system dysregulation. Patwari PP; Stewart TM; Rand CM; Carroll MS; Kuntz NL; Kenny AS; Brogadir CD; Weese-Mayer DE Pediatr Res; 2012 Mar; 71(3):280-5. PubMed ID: 22278185 [TBL] [Abstract][Full Text] [Related]
3. In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome. Weese-Mayer DE; Berry-Kravis EM; Marazita ML Respir Physiol Neurobiol; 2005 Nov; 149(1-3):73-82. PubMed ID: 16054879 [TBL] [Abstract][Full Text] [Related]
8. Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE. Hung CC; Su YN; Tsao PN; Chen PC; Lin SJ; Lin CH; Mu SC; Liu CA; Chang YC; Lin WL; Hsieh WS; Hsu SM Electrophoresis; 2007 Mar; 28(6):894-9. PubMed ID: 17300129 [TBL] [Abstract][Full Text] [Related]
10. PHOX2B in respiratory control: lessons from congenital central hypoventilation syndrome and its mouse models. Amiel J; Dubreuil V; Ramanantsoa N; Fortin G; Gallego J; Brunet JF; Goridis C Respir Physiol Neurobiol; 2009 Aug; 168(1-2):125-32. PubMed ID: 19712905 [TBL] [Abstract][Full Text] [Related]
11. Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome. Di Lascio S; Bachetti T; Saba E; Ceccherini I; Benfante R; Fornasari D Neurobiol Dis; 2013 Feb; 50():187-200. PubMed ID: 23103552 [TBL] [Abstract][Full Text] [Related]
12. PHOX2B mutation-confirmed congenital central hypoventilation syndrome: presentation in adulthood. Antic NA; Malow BA; Lange N; McEvoy RD; Olson AL; Turkington P; Windisch W; Samuels M; Stevens CA; Berry-Kravis EM; Weese-Mayer DE Am J Respir Crit Care Med; 2006 Oct; 174(8):923-7. PubMed ID: 16873766 [TBL] [Abstract][Full Text] [Related]
13. Congenital central hypoventilation syndrome and the PHOX2B gene mutation. Marion TL; Bradshaw WT Neonatal Netw; 2011; 30(6):397-401. PubMed ID: 22052119 [TBL] [Abstract][Full Text] [Related]
14. Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome. Cross SH; Morgan JE; Pattyn A; West K; McKie L; Hart A; Thaung C; Brunet JF; Jackson IJ Hum Mol Genet; 2004 Jul; 13(14):1433-9. PubMed ID: 15150159 [TBL] [Abstract][Full Text] [Related]
15. Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b. Weese-Mayer DE; Berry-Kravis EM; Zhou L; Maher BS; Silvestri JM; Curran ME; Marazita ML Am J Med Genet A; 2003 Dec; 123A(3):267-78. PubMed ID: 14608649 [TBL] [Abstract][Full Text] [Related]
16. Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers. Jennings LJ; Yu M; Zhou L; Rand CM; Berry-Kravis EM; Weese-Mayer DE Diagn Mol Pathol; 2010 Dec; 19(4):224-31. PubMed ID: 21051998 [TBL] [Abstract][Full Text] [Related]
17. Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype. Berry-Kravis EM; Zhou L; Rand CM; Weese-Mayer DE Am J Respir Crit Care Med; 2006 Nov; 174(10):1139-44. PubMed ID: 16888290 [TBL] [Abstract][Full Text] [Related]
18. Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse). Trochet D; de Pontual L; Estêvao MH; Mathieu Y; Munnich A; Feingold J; Goridis C; Lyonnet S; Amiel J Hum Mutat; 2008 May; 29(5):770. PubMed ID: 18407552 [TBL] [Abstract][Full Text] [Related]
19. A respiratory/Hirschsprung phenotype in a three-generation family associated with a novel pathogenic PHOX2B splice donor mutation. Pace NP; Pace Bardon M; Borg I Mol Genet Genomic Med; 2020 Dec; 8(12):e1528. PubMed ID: 33047879 [TBL] [Abstract][Full Text] [Related]
20. [Congenital central hypoventilation syndrome: paradigm shifts and future prospects]. Hayasaka K; Sasaki A Nihon Rinsho; 2014 Feb; 72(2):363-70. PubMed ID: 24605541 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]