244 related articles for article (PubMed ID: 19274556)
1. Congenital central hypoventilation syndrome (CCHS) with Hirschsprung disease (Haddad syndrome): an unusual cause of reduced baseline variability of the fetal heart rate.
Majumdar S; Wood P
J Obstet Gynaecol; 2009 Feb; 29(2):152-3. PubMed ID: 19274556
[No Abstract] [Full Text] [Related]
2. Case report of Haddad syndrome in a newborn: congenital central hypoventilation syndrome and Hirschsprung's disease.
Dejhalla M; Parton P; Golombek SG
J Perinatol; 2006 Apr; 26(4):259-60. PubMed ID: 16570083
[TBL] [Abstract][Full Text] [Related]
3. [Ondine syndrome or central congenital hypoventilation syndrome].
Trang H
Rev Prat; 2006 Jan; 56(2):125-8. PubMed ID: 16584036
[TBL] [Abstract][Full Text] [Related]
4. Congenital hypoventilation syndrome and Hirschsprung's disease - Haddad syndrome: A neonatal case presentation.
Jaiyeola P; El-Metwally D; Viscardi R; Greene C; Woo H
J Neonatal Perinatal Med; 2015; 8(2):165-8. PubMed ID: 26410442
[TBL] [Abstract][Full Text] [Related]
5. Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.
Lai D; Schroer B
J Child Neurol; 2008 Mar; 23(3):341-3. PubMed ID: 18230845
[TBL] [Abstract][Full Text] [Related]
6. Haddad syndrome: a case study.
Shuman L; Youmans D
Neonatal Netw; 2005; 24(4):41-4. PubMed ID: 16117243
[TBL] [Abstract][Full Text] [Related]
7. PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.
Or SF; Tong MF; Lo FM; Law CW; Miu TY; Trochet D; Lam TS
Chin Med J (Engl); 2006 Oct; 119(20):1749-52. PubMed ID: 17097025
[No Abstract] [Full Text] [Related]
8. 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]
9. Concomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation.
Ou-Yang MC; Yang SN; Hsu YM; Ou-Yang MH; Haung HC; Lee SY; Hsieh WS; Su YN; Liu CA
J Pediatr Surg; 2007 Feb; 42(2):e9-11. PubMed ID: 17270534
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics.
Rajendran GP; Kessler MS; Manning FA
J Perinatol; 2009 Oct; 29(10):712-3. PubMed ID: 19784002
[TBL] [Abstract][Full Text] [Related]
12. Congenital central hypoventilation syndrome and Hirschsprung's disease in an extremely preterm infant.
Bajaj R; Smith J; Trochet D; Pitkin J; Ouvrier R; Graf N; Sillence D; Kluckow M
Pediatrics; 2005 Jun; 115(6):e737-8. PubMed ID: 15930201
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A triple threat: Down syndrome, congenital central hypoventilation syndrome, and Hirschsprung disease.
Jones KL; Pivnick EK; Hines-Dowell S; Weese-Mayer DE; Berry-Kravis EM; Santiago T; Nnorom C; Pourcyrous M
Pediatrics; 2012 Nov; 130(5):e1382-4. PubMed ID: 23045564
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Male infant with shallow respirations.
Listernick R
Pediatr Ann; 2011 Oct; 40(10):476-9. PubMed ID: 21973038
[No Abstract] [Full Text] [Related]
20. Anesthetic management of a child with congenital central hypoventilation syndrome (CCHS, Ondine's curse) for dental treatment.
Ishibashi H; Umezawa K; Hayashi S; Shibutani K
Anesth Prog; 2004; 51(3):102-4. PubMed ID: 15497300
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
