187 related articles for article (PubMed ID: 19844731)
1. Novel neuropathologic findings in the Haddad syndrome.
Tomycz ND; Haynes RL; Schmidt EF; Ackerson K; Kinney HC
Acta Neuropathol; 2010 Feb; 119(2):261-9. PubMed ID: 19844731
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Congenital central hypoventilation syndrome and Hirschsprung's disease.
Croaker GD; Shi E; Simpson E; Cartmill T; Cass DT
Arch Dis Child; 1998 Apr; 78(4):316-22. PubMed ID: 9623393
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. A novel PHOX2B gene mutation in an extremely low birth weight infant with congenital central hypoventilation syndrome and variant Hirschsprung's disease.
Miura Y; Watanabe T; Uchida T; Nawa T; Endo N; Fukuzawa T; Ohkubo R; Takeyama J; Sasaki A; Hayasaka K
Eur J Med Genet; 2019 Sep; 62(9):103541. PubMed ID: 30227298
[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 novel association with BRAF mutation.
Al Dakhoul S
J Neonatal Perinatal Med; 2017; 10(4):455-457. PubMed ID: 29286936
[TBL] [Abstract][Full Text] [Related]
12. Haddad syndrome--congenital central hypoventilation associated with Hirschsprung's disease.
D'Souza S; Khubchandani RP
Indian J Pediatr; 2003 Jul; 70(7):597-9. PubMed ID: 12940386
[TBL] [Abstract][Full Text] [Related]
13. Successful redo pull-through for Hirschsprung's disease in a Haddad syndrome patient.
Lee JT; Liu C; Tsai HL; Chin T; Wei CF
J Chin Med Assoc; 2010 Aug; 73(8):438-40. PubMed ID: 20728857
[TBL] [Abstract][Full Text] [Related]
14. Hirschsprung's disease associated with Ondine's curse.
Varma RR; Narayanankutty PK; Rajagopalan K; Rajeevan K
Indian J Pediatr; 2002 Nov; 69(11):987-8. PubMed ID: 12503667
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Neonatal Congenital Central Hypoventilation Syndrome: Why We Should not Sleep on it. Literature Review of Forty-two Neonatal Onset Cases.
Bardanzellu F; Pintus MC; Fanos V; Marcialis MA
Curr Pediatr Rev; 2019; 15(3):139-153. PubMed ID: 31223092
[TBL] [Abstract][Full Text] [Related]
18. Clinical features of children with Haddad syndrome: A single-center experience.
Woo HY; Oh C; Han JW; Kim HY; Jung SE
J Pediatr Surg; 2020 Mar; 55(3):387-392. PubMed ID: 30850150
[TBL] [Abstract][Full Text] [Related]
19. Sonographic findings of total colonic aganglionosis in a neonate with Haddad syndrome: A case report.
Lim YJ; Jung HK
J Clin Ultrasound; 2022 Jul; 50(6):810-813. PubMed ID: 35080777
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]