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Journal Abstract Search

215 related items for PubMed ID: 29738021

  • 1. 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
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  • 2. [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
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  • 4. 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
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  • 6. A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea.
    Amimoto Y, Okada K, Nakano H, Sasaki A, Hayasaka K, Odajima H.
    J Clin Sleep Med; 2014 Mar 15; 10(3):327-9. PubMed ID: 24634632
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  • 7. [Congenital central hypoventilation syndrome, report of three cases].
    Wang Y, He XY, Yang Y, Chen XC.
    Zhonghua Er Ke Za Zhi; 2013 Nov 15; 51(11):852-5. PubMed ID: 24484562
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  • 8. Congenital central hypoventilation syndrome and the PHOX2B gene mutation.
    Marion TL, Bradshaw WT.
    Neonatal Netw; 2011 Nov 15; 30(6):397-401. PubMed ID: 22052119
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  • 9. 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 15; 16(4):951-5. PubMed ID: 22102181
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  • 12. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun 15; 11(3):167-72. PubMed ID: 21730909
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  • 15. Severe Positional Central Sleep Apnea in an Asymptomatic Adult With a PHOX2B Frameshift Mutation.
    Janssen HCJP, Vulto-van Silfhout AT, Jongmans MCJ, van der Hout AH, Overeem S.
    J Clin Sleep Med; 2018 Aug 15; 14(8):1427-1430. PubMed ID: 30092902
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  • 17. Late-onset congenital central hypoventilation syndrome and a rare PHOX2B gene mutation.
    Magalhães J, Madureira N, Medeiros R, Fernandes PC, Oufadem M, Amiel J, Estêvão MH, Reis MG.
    Sleep Breath; 2015 Mar 15; 19(1):55-60. PubMed ID: 24792884
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  • 20. Late onset congenital central hypoventilation syndrome after exposure to general anesthesia.
    Mahfouz AK, Rashid M, Khan MS, Reddy P.
    Can J Anaesth; 2011 Dec 15; 58(12):1105-9. PubMed ID: 21989548
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