156 related articles for article (PubMed ID: 36541215)
1. Sleep disturbances in parental caregivers and patients with congenital central hypoventilation syndrome.
Finch CE; Leu RM; Harford KL; Westbrook AL; Kasi AS
J Clin Sleep Med; 2023 Mar; 19(3):549-554. PubMed ID: 36541215
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Impaired ventilation during 6-min walk test in congenital central hypoventilation syndrome.
Ghosh RN; Guglani L; Westbrook AL; Mao CY; Bai S; Keens TG; Kasi AS
Pediatr Pulmonol; 2022 Jul; 57(7):1660-1667. PubMed ID: 35460211
[TBL] [Abstract][Full Text] [Related]
4. Images: Atypical presentation of congenital central hypoventilation syndrome in an infant with central and obstructive sleep apnea.
Fain ME; Raghunandan S; Pencheva B; Leu RM; Kasi AS
J Clin Sleep Med; 2024 Mar; 20(3):478-481. PubMed ID: 37861394
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Congenital central hypoventilation syndrome without hypoventilation: is it congenital central hypoventilation syndrome?
Wo LL; Itani R; Keens TG; Marachelian A; Ji J; Perez IA
J Clin Sleep Med; 2023 Jun; 19(6):1161-1164. PubMed ID: 36798979
[TBL] [Abstract][Full Text] [Related]
7. Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS).
Rand CM; Yu M; Jennings LJ; Panesar K; Berry-Kravis EM; Zhou L; Weese-Mayer DE
Am J Med Genet A; 2012 Sep; 158A(9):2297-301. PubMed ID: 22821709
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea.
Amimoto Y; Okada K; Nakano H; Sasaki A; Hayasaka K; Odajima H
J Clin Sleep Med; 2014 Mar; 10(3):327-9. PubMed ID: 24634632
[TBL] [Abstract][Full Text] [Related]
10. Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel
Schirwani S; Pysden K; Chetcuti P; Blyth M
J Clin Sleep Med; 2017 Nov; 13(11):1359-1362. PubMed ID: 28992836
[TBL] [Abstract][Full Text] [Related]
11. PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndrome.
Wang TC; Su YN; Lai MC
Pediatr Neonatol; 2014 Feb; 55(1):68-70. PubMed ID: 23597545
[TBL] [Abstract][Full Text] [Related]
12. Characteristics and outcomes in children with congenital central hypoventilation syndrome on long-term mechanical ventilation in the Netherlands.
Evers-Bikker EE; de Weerd W; Wijkstra PJ; Corel L; Verweij LP; Vosse BAH
Eur J Pediatr; 2024 Feb; 183(2):791-797. PubMed ID: 38001308
[TBL] [Abstract][Full Text] [Related]
13. Atypical presentations associated with non-polyalanine repeat PHOX2B mutations.
Katwa U; D'Gama AM; Qualls AE; Donovan LM; Heffernan J; Shi J; Agrawal PB
Am J Med Genet A; 2018 Jul; 176(7):1627-1631. PubMed ID: 29704303
[TBL] [Abstract][Full Text] [Related]
14. Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family members.
Sivan Y; Zhou A; Jennings LJ; Berry-Kravis EM; Yu M; Zhou L; Rand CM; Weese-Mayer DE
Am J Med Genet A; 2019 Mar; 179(3):503-506. PubMed ID: 30672101
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Congenital Central Hypoventilation Syndrome: Diagnosis and Long-Term Ventilatory Outcomes.
Fain ME; Westbrook AL; Kasi AS
Clin Med Insights Pediatr; 2023; 17():11795565231169556. PubMed ID: 37256017
[TBL] [Abstract][Full Text] [Related]
17. Two novel mutations in exon 3 of PHOX2B gene: think about congenital central hypoventilation syndrome in patients with Hirschsprung disease.
Paglietti MG; Cherchi C; Porcaro F; Agolini E; Schiavino A; Petreschi F; Novelli A; Cutrera R
Ital J Pediatr; 2019 Apr; 45(1):49. PubMed ID: 30999961
[TBL] [Abstract][Full Text] [Related]
18. A Novel c.676_677insG
Ye G; Han D; Jiang Y; Wang Z; Zhou Y; Lin X; Chen W; Chen M; Xu J; Yang Y; Guo Q
J Clin Sleep Med; 2019 Mar; 15(3):509-513. PubMed ID: 30853048
[No Abstract] [Full Text] [Related]
19. 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]
20. Hyperthyroidism hidden by congenital central hypoventilation syndrome.
Fox DA; Weese-Mayer DE; Wensley DF; Stewart LL
J Pediatr Endocrinol Metab; 2015 May; 28(5-6):705-8. PubMed ID: 25581741
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]