These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 37951652)

  • 1. Later Onset Congenital Central Hypoventilation Syndrome.
    Amos L
    Med Clin North Am; 2024 Jan; 108(1):215-226. PubMed ID: 37951652
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital central hypoventilation syndrome without hypoventilation: is it congenital central hypoventilation syndrome?
    Wo LL; Itani R; Keens TG; Marachelian A; Ji J; Perez IA
    J Clin Sleep Med; 2023 Jun; 19(6):1161-1164. PubMed ID: 36798979
    [TBL] [Abstract][Full Text] [Related]  

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

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital central hypoventilation syndrome in korea: 20 years of clinical observation and evaluation of the ventilation strategy in a single center.
    Lee MJ; Park JS; Kim K; Ko JM; Park JD; Suh DI
    Eur J Pediatr; 2024 Aug; 183(8):3479-3487. PubMed ID: 38780650
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 179(3):503-506. PubMed ID: 30672101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 19(1):55-60. PubMed ID: 24792884
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adult With
    Kasi AS; Kun SS; Keens TG; Perez IA
    J Clin Sleep Med; 2018 Dec; 14(12):2079-2081. PubMed ID: 30518452
    [No Abstract]   [Full Text] [Related]  

  • 10. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 10(3):327-9. PubMed ID: 24634632
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Guidelines for diagnosis and management of congenital central hypoventilation syndrome.
    Trang H; Samuels M; Ceccherini I; Frerick M; Garcia-Teresa MA; Peters J; Schoeber J; Migdal M; Markstrom A; Ottonello G; Piumelli R; Estevao MH; Senecic-Cala I; Gnidovec-Strazisar B; Pfleger A; Porto-Abal R; Katz-Salamon M
    Orphanet J Rare Dis; 2020 Sep; 15(1):252. PubMed ID: 32958024
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Rare cause of neonatal apnea from congenital central hypoventilation syndrome.
    Tovichien P; Rattananont K; Kulthamrongsri N; Chanvanichtrakool M; Yangthara B
    BMC Pediatr; 2022 Feb; 22(1):105. PubMed ID: 35209861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.
    Khorasanian R; Mojbafan M; Khosravi N
    Mol Biol Rep; 2021 Dec; 48(12):8239-8243. PubMed ID: 34626313
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. Anesthetic Considerations for Patients With Congenital Central Hypoventilation Syndrome: A Systematic Review of the Literature.
    Basu SM; Chung FF; AbdelHakim SF; Wong J
    Anesth Analg; 2017 Jan; 124(1):169-178. PubMed ID: 27918326
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 8.