BACKGROUND
Right heart catheterization is the gold standard for diagnosis and monitoring of pediatric pulmonary hypertension (PH). Noninvasive cardiovascular magnetic resonance (CMR) and echocardiography can additionally provide volumetric and functional assessment of the right ventricle and possibly serve as a non-inv...
Takashi Fujiwara, Vivian Lu, B. Frank et al.· Journal of Cardiovascular Ma...· 0 citations
Neonatal pulmonary hypertension (PH) can be categorized into three distinct physiologies: resistance-driven precapillary pulmonary arterial hypertension (PAH), flow-driven precapillary PH, and postcapillary PH. We present eight patients, divided into three groups: premature infants with BPD, infants with chronic respir...
T. Gonzalez, C. Simpkin, Paula Dias Maia et al.· Frontiers in Pediatrics· 0 citations
Pulmonary hypertension (PH) may complicate a broad range of genetic syndromes beyond the established spectrum of heritable pulmonary arterial hypertension. Although these conditions are individually rare, together they represent an emerging field at the crossroads of developmental biology, vascular medicine, and precis...
Julien Grynblat, Florence Coulet, T. Lacoste-Palasset et al.· European Respiratory Journal· 0 citations
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