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Journal Abstract Search
103 related items for PubMed ID: 16191289
1. [Congenital central hypoventilation syndrome: report of a case]. Xu ZF, Jiang ZF. Zhonghua Er Ke Za Zhi; 2005 Aug; 43(8):636-7. PubMed ID: 16191289 [No Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
4. Haddad syndrome presenting with abdominal distension associated with long-segment aganglionosis. Chung WD, Lim GY, Kim SY, Chung JH, Kim SJ. Clin Imaging; 2012 Mar; 36(2):149-52. PubMed ID: 22370137 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. 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]
10. Sleep hypoventilation syndrome and respiratory failure due to multifocal motor neuropathy with conduction block. Kyriakides T, Papacostas S, Papanicolaou E, Bagdades E, Papathanasiou ES. Muscle Nerve; 2011 Apr; 43(4):610-4. PubMed ID: 21404292 [Abstract] [Full Text] [Related]
13. Late onset hypoventilation syndrome: is there a spectrum of idiopathic hypoventilation syndromes? Gothi D, Joshi JM. Indian J Chest Dis Allied Sci; 2005 Apr; 47(4):293-7. PubMed ID: 16255402 [Abstract] [Full Text] [Related]
16. [Non-invasive mechanical ventilation in a child with central hypoventilation syndrome: one year follow-up]. Xu Z, Jia X, Bai P, Shen K. Zhonghua Er Ke Za Zhi; 2014 Feb; 52(2):117-21. PubMed ID: 24739723 [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 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]