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Journal Abstract Search

186 related items for PubMed ID: 35882978

  • 21. 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
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  • 22. Causative and common PHOX2B variants define a broad phenotypic spectrum.
    Bachetti T, Ceccherini I.
    Clin Genet; 2020 Jan; 97(1):103-113. PubMed ID: 31444792
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  • 25. Congenital central hypoventilation syndrome: PHOX2B genotype determines risk for sudden death.
    Gronli JO, Santucci BA, Leurgans SE, Berry-Kravis EM, Weese-Mayer DE.
    Pediatr Pulmonol; 2008 Jan; 43(1):77-86. PubMed ID: 18041756
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  • 28. Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.
    Weese-Mayer DE, Rand CM, Berry-Kravis EM, Jennings LJ, Loghmanee DA, Patwari PP, Ceccherini I.
    Pediatr Pulmonol; 2009 Jun; 44(6):521-35. PubMed ID: 19422034
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  • 32. [Congenital central hypoventilation syndrome: analysis of PHOX2B gene mutation in a case].
    Yan Y, Yi B, Liu D, Zhao F, Zhang C, Chen X, Hao S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):665-9. PubMed ID: 26418987
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  • 34. Hirschsprung disease and other gastrointestinal motility disorders in patients with CCHS.
    Balakrishnan K, Perez IA, Keens TG, Sicolo A, Punati J, Danialifar T.
    Eur J Pediatr; 2021 Feb; 180(2):469-473. PubMed ID: 33113016
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