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Journal Abstract Search
265 related items for PubMed ID: 9623393
1. 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 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. 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 Sep; 54(5):519-22. PubMed ID: 23427517 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. [Neurocristopathy. The association of Hirschsprung's disease-ganglioneuroma with autonomic nervous system dysfunction in 2 children]. Levard G, Boige N, Vitoux C, Aigrain Y, Boureau M, Navarro J. Arch Fr Pediatr; 1989 Oct; 46(8):595-7. PubMed ID: 2604514 [Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
13. Hirschsprung's disease associated with Ondine's curse: a special subgroup? Nakahara S, Yokomori K, Tamura K, Oku K, Tsuchida Y. J Pediatr Surg; 1995 Oct; 30(10):1481-4. PubMed ID: 8786495 [Abstract] [Full Text] [Related]
17. Hirschsprung's disease, Ondine's curse, and neuroblastoma--manifestations of neurocristopathy. Roshkow JE, Haller JO, Berdon WE, Sane SM. Pediatr Radiol; 1988 Oct; 19(1):45-9. PubMed ID: 3222062 [Abstract] [Full Text] [Related]
18. Hirschsprung's disease and Ondine's curse: further evidence for a distinct syndrome. Minutillo C, Pemberton PJ, Goldblatt J. Clin Genet; 1989 Sep; 36(3):200-3. PubMed ID: 2791333 [Abstract] [Full Text] [Related]
19. Congenital central hypoventilation syndrome and Hirschsprung disease: A retrospective review of the French National Registry Center on 33 cases. Broch A, Trang H, Montalva L, Berrebi D, Dauger S, Bonnard A. J Pediatr Surg; 2019 Nov; 54(11):2325-2330. PubMed ID: 30879749 [Abstract] [Full Text] [Related]