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Journal Abstract Search

193 related items for PubMed ID: 22102181

  • 1. 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]

  • 2. Adult With PHOX2B Mutation and Late-Onset Congenital Central Hypoventilation Syndrome.
    Kasi AS, Kun SS, Keens TG, Perez IA.
    J Clin Sleep Med; 2018 Dec 15; 14(12):2079-2081. PubMed ID: 30518452
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  • 4. Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.
    Al Saadi MM.
    Sleep Breath; 2011 Dec 15; 15(4):875-8. PubMed ID: 21088916
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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?
    Nirupam N, Sharma R, Chhapola V, Kanwal SK, Berry-Kravis EM, Kumar V.
    Indian J Pediatr; 2013 Aug 15; 80(8):688-90. PubMed ID: 22829249
    [Abstract] [Full Text] [Related]

  • 7. Haddad syndrome.
    Ławicka M, Sawicka J, Bąkowska G.
    Anaesthesiol Intensive Ther; 2013 Aug 15; 45(1):30-2. PubMed ID: 23572305
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  • 9. 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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  • 13. Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family members.
    Sivan Y, Zhou A, Jennings LJ, Berry-Kravis EM, Yu M, Zhou L, Rand CM, Weese-Mayer DE.
    Am J Med Genet A; 2019 Mar 15; 179(3):503-506. PubMed ID: 30672101
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  • 14. 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 15; 39(5):534-535. PubMed ID: 29738021
    [Abstract] [Full Text] [Related]

  • 15. Haddad syndrome novel association with BRAF mutation.
    Al Dakhoul S.
    J Neonatal Perinatal Med; 2017 May 15; 10(4):455-457. PubMed ID: 29286936
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  • 16. Later Onset Congenital Central Hypoventilation Syndrome.
    Amos L.
    Med Clin North Am; 2024 Jan 15; 108(1):215-226. PubMed ID: 37951652
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  • 18. Heterozygous 24-polyalanine repeats in the PHOX2B gene with different manifestations across three generations.
    Chuen-im P, Marwan S, Carter J, Kemp J, Rivera-Spoljaric K.
    Pediatr Pulmonol; 2014 Feb 15; 49(2):E13-6. PubMed ID: 23460419
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  • 19. PHOX2B mutation-confirmed congenital central hypoventilation syndrome in a Chinese family: presentation from newborn to adulthood.
    Lee P, Su YN, Yu CJ, Yang PC, Wu HD.
    Chest; 2009 Feb 15; 135(2):537-544. PubMed ID: 19201717
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  • 20. Congenital central hypoventilation syndrome and the PHOX2B gene mutation.
    Marion TL, Bradshaw WT.
    Neonatal Netw; 2011 Feb 15; 30(6):397-401. PubMed ID: 22052119
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