398 related articles for article (PubMed ID: 25581741)
1. 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]
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. 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]
4. 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]
5. Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children.
Charnay AJ; Antisdel-Lomaglio JE; Zelko FA; Rand CM; Le M; Gordon SC; Vitez SF; Tse JW; Brogadir CD; Nelson MN; Berry-Kravis EM; Weese-Mayer DE
Chest; 2016 Mar; 149(3):809-15. PubMed ID: 26378991
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Sinus vein thrombosis as presenting finding in the congenital central hypoventilation syndrome: an insight on the pathophysiology of the association.
Joseph L; Goldberg S; Shahroor S; Gomori M; Mimouni FB; Picard E
Pediatr Pulmonol; 2011 Aug; 46(8):826-8. PubMed ID: 21465679
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Congenital central hypoventilation syndrome: a neurocristopathy with disordered respiratory control and autonomic regulation.
Rand CM; Carroll MS; Weese-Mayer DE
Clin Chest Med; 2014 Sep; 35(3):535-45. PubMed ID: 25156769
[TBL] [Abstract][Full Text] [Related]
10. Congenital central hypoventilation syndrome: a case report.
Crowell BA; Bissinger RL; Conway-Orgel M
Adv Neonatal Care; 2011 Jun; 11(3):167-72. PubMed ID: 21730909
[TBL] [Abstract][Full Text] [Related]
11. Life-threatening cardiac arrhythmias in congenital central hypoventilation syndrome.
Laifman E; Keens TG; Bar-Cohen Y; Perez IA
Eur J Pediatr; 2020 May; 179(5):821-825. PubMed ID: 31950261
[TBL] [Abstract][Full Text] [Related]
12. [Congenital central hypoventilation syndrome: analysis of PHOX2B gene mutation in a case].
Yan Y; Yi B; Liu D; Zhao F; Zhang C; Chen X; Hao S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):665-9. PubMed ID: 26418987
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Congenital central hypoventilation syndrome with hirschsprung's disease due to PHOX2B gene mutation in a Turkish infant.
Kaymakçi A; Narter F; Yazar AS; Yilmaz MS
Turk J Pediatr; 2012; 54(5):519-22. PubMed ID: 23427517
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Heterozygous 24-polyalanine repeats in the PHOX2B gene with different manifestations across three generations.
Chuen-im P; Marwan S; Carter J; Kemp J; Rivera-Spoljaric K
Pediatr Pulmonol; 2014 Feb; 49(2):E13-6. PubMed ID: 23460419
[TBL] [Abstract][Full Text] [Related]
19. Residual chemosensitivity to ventilatory challenges in genotyped congenital central hypoventilation syndrome.
Carroll MS; Patwari PP; Kenny AS; Brogadir CD; Stewart TM; Weese-Mayer DE
J Appl Physiol (1985); 2014 Feb; 116(4):439-50. PubMed ID: 24381123
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]