186 related articles for article (PubMed ID: 27340804)
1. Congenital Tonic Pupils Associated With Congenital Central Hypoventilation Syndrome and Hirschsprung Disease.
Mehta VJ; Ling JJ; Martinez EG; Reddy AC; Donahue SP
J Neuroophthalmol; 2016 Dec; 36(4):414-416. PubMed ID: 27340804
[TBL] [Abstract][Full Text] [Related]
2. Tonic pupil associated with congenital neuroblastoma, Hirschsprung disease, and central hypoventilation syndrome.
Lambert SR; Yang LL; Stone C
Am J Ophthalmol; 2000 Aug; 130(2):238-40. PubMed ID: 11004304
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Variable human phenotype associated with novel deletions of the PHOX2B gene.
Jennings LJ; Yu M; Rand CM; Kravis N; Berry-Kravis EM; Patwari PP; Weese-Mayer DE
Pediatr Pulmonol; 2012 Feb; 47(2):153-61. PubMed ID: 21830319
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Congenital central hypoventilation syndrome associated with Hirschsprung's Disease: case report and literature review.
Sandoval RL; Zaconeta CM; Margotto PR; Cardoso MT; França EM; Medina CT; Canó TM; Faria AS
Rev Paul Pediatr; 2016 Sep; 34(3):374-8. PubMed ID: 26838603
[TBL] [Abstract][Full Text] [Related]
8. An unusual cause of fetal hypomobility:congenital central hypoventilation syndrome associated with hirschsprung disease.
De Montpellier S; Sznajer Y; Amiel J; Francois G; Nassogne MC; Debauche C; Scheers I
Eur J Pediatr; 2014 Dec; 173(12):1607-9. PubMed ID: 24135798
[TBL] [Abstract][Full Text] [Related]
9. Neonatal Hirschsprung disease, dysautonomia, and central hypoventilation.
Sagel SD; Cohen H; Townsend SF
Obstet Gynecol; 1999 May; 93(5 Pt 2):834-6. PubMed ID: 10912412
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Haddad syndrome with PHOX2B gene mutation in a Korean infant.
Lee CW; Lee JH; Jung EY; Choi SO; Kim CS; Lee SL; Kim DK
J Korean Med Sci; 2011 Feb; 26(2):312-5. PubMed ID: 21286029
[TBL] [Abstract][Full Text] [Related]
12. Congenital central hypoventilation syndrome and sudden infant death syndrome: disorders of autonomic regulation.
Rand CM; Patwari PP; Carroll MS; Weese-Mayer DE
Semin Pediatr Neurol; 2013 Mar; 20(1):44-55. PubMed ID: 23465774
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Male infant with shallow respirations.
Listernick R
Pediatr Ann; 2011 Oct; 40(10):476-9. PubMed ID: 21973038
[No Abstract] [Full Text] [Related]
17. 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]
18. Haddad syndrome presenting with abdominal distension associated with long-segment aganglionosis.
Chung WD; Lim GY; Kim SY; Chung JH; Kim SJ
Clin Imaging; 2012; 36(2):149-52. PubMed ID: 22370137
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
