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Journal Abstract Search

233 related items for PubMed ID: 24182656

  • 1. [ATS clinical policy statement: congenital central hypoventilation syndrome. Genetic basis, diagnosis and management].
    Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Keens TG, Loghmanee DA, Trang H, sous-commission « syndrome d’hypoventilation alvéolaire centrale congénitale » de l’American Thoracic Society.
    Rev Mal Respir; 2013 Oct; 30(8):706-33. PubMed ID: 24182656
    [No Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Unusual case of central alveolar hypoventilation. Lessons learned from ventilatory management of patients with alveolar hypoventilation in critical care conditions.
    Briones Claudett KH, Grunauer M.
    Saudi Med J; 2018 May; 39(5):534-535. PubMed ID: 29738021
    [Abstract] [Full Text] [Related]

  • 4. Haddad syndrome.
    Ławicka M, Sawicka J, Bąkowska G.
    Anaesthesiol Intensive Ther; 2013 May; 45(1):30-2. PubMed ID: 23572305
    [Abstract] [Full Text] [Related]

  • 5. [Spotlight on the congenital central hypoventilation syndrome (Ondine's curse) and its management].
    Trang H, Amiel J, Straus C.
    Rev Mal Respir; 2013 Oct; 30(8):609-12. PubMed ID: 24182648
    [No Abstract] [Full Text] [Related]

  • 6. Congenital central hypoventilation syndrome and the PHOX2B gene mutation.
    Marion TL, Bradshaw WT.
    Neonatal Netw; 2011 Oct; 30(6):397-401. PubMed ID: 22052119
    [Abstract] [Full Text] [Related]

  • 7. [Congenital central hypoventilation syndrome: paradigm shifts and future prospects].
    Hayasaka K, Sasaki A.
    Nihon Rinsho; 2014 Feb; 72(2):363-70. PubMed ID: 24605541
    [Abstract] [Full Text] [Related]

  • 8. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun; 11(3):167-72. PubMed ID: 21730909
    [Abstract] [Full Text] [Related]

  • 9. Autonomic dysfunction of glucose homoeostasis in congenital central hypoventilation syndrome.
    Marics G, Amiel J, Vatai B, Lódi C, Mikos B, Tóth-Heyn P.
    Acta Paediatr; 2013 Apr; 102(4):e178-80. PubMed ID: 23231723
    [No Abstract] [Full Text] [Related]

  • 10. Late onset congenital central hypoventilation syndrome after exposure to general anesthesia.
    Mahfouz AK, Rashid M, Khan MS, Reddy P.
    Can J Anaesth; 2011 Dec; 58(12):1105-9. PubMed ID: 21989548
    [Abstract] [Full Text] [Related]

  • 11. [Congenital central hypoventilation syndrome, report of three cases].
    Wang Y, He XY, Yang Y, Chen XC.
    Zhonghua Er Ke Za Zhi; 2013 Nov; 51(11):852-5. PubMed ID: 24484562
    [Abstract] [Full Text] [Related]

  • 12. Case reports of congenital central hypoventilation syndrome.
    Marsh K, Ehrhardt E.
    Neonatal Netw; 2012 Nov; 31(3):157-61. PubMed ID: 22564311
    [Abstract] [Full Text] [Related]

  • 13. Congenital central hypoventilation syndrome: diagnosis and management.
    Maloney MA, Kun SS, Keens TG, Perez IA.
    Expert Rev Respir Med; 2018 Apr; 12(4):283-292. PubMed ID: 29486608
    [Abstract] [Full Text] [Related]

  • 14. 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 Apr; 8(2):165-8. PubMed ID: 26410442
    [Abstract] [Full Text] [Related]

  • 15. Male infant with shallow respirations.
    Listernick R.
    Pediatr Ann; 2011 Oct; 40(10):476-9. PubMed ID: 21973038
    [No Abstract] [Full Text] [Related]

  • 16. Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.
    Al Saadi MM.
    Sleep Breath; 2011 Dec; 15(4):875-8. PubMed ID: 21088916
    [No Abstract] [Full Text] [Related]

  • 17. Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.
    Bittencourt LR, Pedrazzoli M, Yagihara F, Luz GP, Garbuio S, Moreira GA, Perfeito JA, Tufik S.
    Sleep Breath; 2012 Dec; 16(4):951-5. PubMed ID: 22102181
    [No Abstract] [Full Text] [Related]

  • 18. Haddad syndrome novel association with BRAF mutation.
    Al Dakhoul S.
    J Neonatal Perinatal Med; 2017 Dec; 10(4):455-457. PubMed ID: 29286936
    [Abstract] [Full Text] [Related]

  • 19. A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndrome.
    Guzoglu N, Aslan MK, Gunay YD, Atasoy P, Ceylaner S, Aliefendioglu D.
    Clin Dysmorphol; 2020 Jul; 29(3):152-154. PubMed ID: 32073407
    [No 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]

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