233 related articles for article (PubMed ID: 36403185)
1. Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndrome.
Slattery SM; Perez IA; Ceccherini I; Chen ML; Kurek KC; Yap KL; Keens TG; Khaytin I; Ballard HA; Sokol EA; Mittal A; Rand CM; Weese-Mayer DE
Clin Auton Res; 2023 Jun; 33(3):231-249. PubMed ID: 36403185
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.
Weese-Mayer DE; Berry-Kravis EM; Ceccherini I; Keens TG; Loghmanee DA; Trang H;
Am J Respir Crit Care Med; 2010 Mar; 181(6):626-44. PubMed ID: 20208042
[TBL] [Abstract][Full Text] [Related]
4. Anesthetic Considerations for Patients With Congenital Central Hypoventilation Syndrome: A Systematic Review of the Literature.
Basu SM; Chung FF; AbdelHakim SF; Wong J
Anesth Analg; 2017 Jan; 124(1):169-178. PubMed ID: 27918326
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene.
Repetto GM; Corrales RJ; Abara SG; Zhou L; Berry-Kravis EM; Rand CM; Weese-Mayer DE
Acta Paediatr; 2009 Jan; 98(1):192-5. PubMed ID: 18798833
[TBL] [Abstract][Full Text] [Related]
9. Central congenital hypoventilation syndrome: changing face of a less mysterious but more complex genetic disorder.
Grigg-Damberger M; Wells A
Semin Respir Crit Care Med; 2009 Jun; 30(3):262-74. PubMed ID: 19452387
[TBL] [Abstract][Full Text] [Related]
10. PHOX2B mutation-confirmed congenital central hypoventilation syndrome in a Chinese family: presentation from newborn to adulthood.
Lee P; Su YN; Yu CJ; Yang PC; Wu HD
Chest; 2009 Feb; 135(2):537-544. PubMed ID: 19201717
[TBL] [Abstract][Full Text] [Related]
11. Variable phenotypes in congenital central hypoventilation syndrome with
Kasi AS; Li H; Jurgensen TJ; Guglani L; Keens TG; Perez IA
J Clin Sleep Med; 2021 Oct; 17(10):2049-2055. PubMed ID: 33983112
[TBL] [Abstract][Full Text] [Related]
12. Expanding the phenotype of congenital central hypoventilation syndrome impacts management decisions.
Byers HM; Chen M; Gelfand AS; Ong B; Jendras M; Glass IA
Am J Med Genet A; 2018 Jun; 176(6):1398-1404. PubMed ID: 29696799
[TBL] [Abstract][Full Text] [Related]
13. Congenital central hypoventilation syndrome: neurocognitive functioning in school age children.
Zelko FA; Nelson MN; Leurgans SE; Berry-Kravis EM; Weese-Mayer DE
Pediatr Pulmonol; 2010 Jan; 45(1):92-8. PubMed ID: 19960523
[TBL] [Abstract][Full Text] [Related]
14. Adult cases of late-onset congenital central hypoventilation syndrome and paired-like homeobox 2B-mutation carriers: an additional case report and pooled analysis.
Hino A; Terada J; Kasai H; Shojima H; Ohgino K; Sasaki A; Hayasaka K; Tatsumi K
J Clin Sleep Med; 2020 Nov; 16(11):1891-1900. PubMed ID: 32741443
[TBL] [Abstract][Full Text] [Related]
15. Congenital central hypoventilation syndrome: diagnosis and management.
Maloney MA; Kun SS; Keens TG; Perez IA
Expert Rev Respir Med; 2018 Apr; 12(4):283-292. PubMed ID: 29486608
[TBL] [Abstract][Full Text] [Related]
16. Guidelines for diagnosis and management of congenital central hypoventilation syndrome.
Trang H; Samuels M; Ceccherini I; Frerick M; Garcia-Teresa MA; Peters J; Schoeber J; Migdal M; Markstrom A; Ottonello G; Piumelli R; Estevao MH; Senecic-Cala I; Gnidovec-Strazisar B; Pfleger A; Porto-Abal R; Katz-Salamon M
Orphanet J Rare Dis; 2020 Sep; 15(1):252. PubMed ID: 32958024
[TBL] [Abstract][Full Text] [Related]
17. Congenital central hypoventilation syndrome: a bedside-to-bench success story for advancing early diagnosis and treatment and improved survival and quality of life.
Weese-Mayer DE; Rand CM; Zhou A; Carroll MS; Hunt CE
Pediatr Res; 2017 Jan; 81(1-2):192-201. PubMed ID: 27673423
[TBL] [Abstract][Full Text] [Related]
18. Vagal and sympathetic heart rate and blood pressure control in adult onset PHOX2B mutation-confirmed congenital central hypoventilation syndrome.
Diedrich A; Malow BA; Antic NA; Sato K; McEvoy RD; Mathias CJ; Robertson D; Berry-Kravis EM; Weese-Mayer DE
Clin Auton Res; 2007 Jun; 17(3):177-85. PubMed ID: 17541758
[TBL] [Abstract][Full Text] [Related]
19. Adult With
Kasi AS; Kun SS; Keens TG; Perez IA
J Clin Sleep Med; 2018 Dec; 14(12):2079-2081. PubMed ID: 30518452
[No Abstract] [Full Text] [Related]
20. Developmental disorders affecting the respiratory system: CCHS and ROHHAD.
Ceccherini I; Kurek KC; Weese-Mayer DE
Handb Clin Neurol; 2022; 189():53-91. PubMed ID: 36031316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
