Pulmonary interstitial glycogenosis: An unrecognized etiology of persistent pulmonary hypertension of the newborn in congenital heart disease?

Autor: Fineman, Jeffrey, Oishi, Peter, Radman, MR, Goldhoff, P, Jones, KD, Azakie, A, Datar, S, Adatia, I, Fineman, JR
Jazyk: angličtina
Rok vydání: 2013
Zdroj: Fineman, Jeffrey; Oishi, Peter; Radman, MR; Goldhoff, P; Jones, KD; Azakie, A; et al.(2013). Pulmonary interstitial glycogenosis: An unrecognized etiology of persistent pulmonary hypertension of the newborn in congenital heart disease?. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5790m20v
Popis: Background: Pulmonary interstitial glycogenosis (PIG) arises from a developmental disorder of the pulmonary mesenchyme and presents clinically with reversible neonatal respiratory distress and/or persistent pulmonary hypertension of the newborn (PPHN). Obj
Databáze: OpenAIRE