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Multiomics endotyping of preterm infants with bronchopulmonary dysplasia and pulmonary hypertension—A pilot study

Pulmonary circulation, 2023-04, Vol.13 (2), p.e12232-n/a

2023

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Insulin‐like growth factor binding Protein‐4: A novel indicator of pulmonary arterial hypertension severity and survival

Pulmonary circulation, 2023-04, Vol.13 (2), p.e12235-n/a

2023

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Caveolin‐1 associated with severe (pediatric‐onset) presentation of pulmonary arterial hypertension

Pulmonary circulation, 2022-07, Vol.12 (3), p.n/a

2022

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Liver abnormalities in pulmonary arterial hypertension

Pulmonary Circulation, 2021-10, Vol.11 (4), p.1-12

2021

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Transpulmonary generation of cell‐free hemoglobin contributes to vascular dysfunction in pulmonary arterial hypertension via dysregulated clearance mechanisms

Pulmonary circulation, 2023-01, Vol.13 (1), p.e12185-n/a

2023

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Low-affinity insulin-like growth factor binding protein 7 and its association with pulmonary arterial hypertension severity and survival

Pulmonary circulation, 2023-07, Vol.13 (3), p.e12284-e12284

2023

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Proteomics discovery of pulmonary hypertension biomarkers: Insulin‐like growth factor binding proteins are associated with disease severity

Pulmonary circulation, 2022-04, Vol.12 (2), p.e12039-n/a

2022

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Gender, sex hormones and pulmonary hypertension

Pulmonary Circulation, 2013-04, Vol.3 (2), p.294-314

2013

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Estrogen metabolites in a small cohort of patients with idiopathic pulmonary arterial hypertension

Pulmonary circulation, 2020-01, Vol.10 (1), p.1-5

2020

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Hepatoma‐derived growth factor is associated with pulmonary vascular remodeling and PAH disease severity and survival

Pulmonary circulation, 2022-01, Vol.12 (1), p.e12007-n/a

2022

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Oral treprostinil in transition or as add-on therapy in pediatric pulmonary arterial hypertension

Pulmonary circulation, 2019-07, Vol.9 (3), p.1-8

2019

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Novel early life risk factors for adult pulmonary hypertension

Pulmonary circulation, 2019-04, Vol.9 (2), p.1-4

2019

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Low-grade albuminuria in pulmonary arterial hypertension

Pulmonary circulation, 2019-04, Vol.9 (2), p.1-9

2019

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Sex hormone exposure and reproductive factors in pulmonary arterial hypertension: a case–control study

Pulmonary circulation, 2020-01, Vol.10 (1), p.1-9

2020

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A checkpoint on innate myeloid cells in pulmonary arterial hypertension

Pulmonary circulation, 2019-01, Vol.9 (1), p.1-5

2019

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The genetics of pulmonary arterial hypertension in the post-BMPR2 era

Pulmonary Circulation, 2011-07, Vol.1 (3), p.305-319

2011

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United States Pulmonary Hypertension Scientific Registry (USPHSR): rationale, design, and clinical implications

Pulmonary circulation, 2019-04, Vol.9 (2), p.1-8

2019

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Dysfunctional BMPR2 signaling drives an abnormal endothelial requirement for glutamine in pulmonary arterial hypertension

Pulmonary circulation, 2017-03, Vol.7 (1), p.186-199

2017

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Impact of diabetes on survival and right ventricular compensation in pulmonary arterial hypertension

Pulmonary circulation, 2014-06, Vol.4 (2), p.311-318

2014

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Pulmonary hypertension’s variegated landscape: a snapshot

Pulmonary Circulation, 2017-01, Vol.7 (1), p.67-81

2017

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Shared Gene Expression Patterns in Mesenchymal Progenitors Derived from Lung and Epidermis in Pulmonary Arterial Hypertension: Identifying Key Pathways in Pulmonary Vascular Disease

Pulmonary circulation, 2016-12, Vol.6 (4), p.483-497

2016

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Shorter survival in familial versus idiopathic pulmonary arterial hypertension is associated with hemodynamic markers of impaired right ventricular function

Pulmonary circulation, 2013-09, Vol.3 (3), p.589-598

2013

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Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression

Pulmonary circulation, 2011-07, Vol.1 (3), p.389-398

2011

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Pulmonary hypertension's variegated landscape: a snapshot

Pulmonary circulation, 2016-12, Article 690552

2016

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Multiomics endotyping of preterm infants with bronchopulmonary dysplasia and pulmonary hypertension—A pilot study

Insulin‐like growth factor binding Protein‐4: A novel indicator of pulmonary arterial hypertension severity and survival

Caveolin‐1 associated with severe (pediatric‐onset) presentation of pulmonary arterial hypertension

Liver abnormalities in pulmonary arterial hypertension

Transpulmonary generation of cell‐free hemoglobin contributes to vascular dysfunction in pulmonary arterial hypertension via dysregulated clearance mechanisms

Kids Mod PAH trial: A multicenter trial comparing mono‐ versus duo‐therapy for initial treatment of pediatric pulmonary hypertension

Low-affinity insulin-like growth factor binding protein 7 and its association with pulmonary arterial hypertension severity and survival

Proteomics discovery of pulmonary hypertension biomarkers: Insulin‐like growth factor binding proteins are associated with disease severity

Gender, sex hormones and pulmonary hypertension

Estrogen metabolites in a small cohort of patients with idiopathic pulmonary arterial hypertension

Hepatoma‐derived growth factor is associated with pulmonary vascular remodeling and PAH disease severity and survival

Oral treprostinil in transition or as add-on therapy in pediatric pulmonary arterial hypertension

Novel early life risk factors for adult pulmonary hypertension

Low-grade albuminuria in pulmonary arterial hypertension

Sex hormone exposure and reproductive factors in pulmonary arterial hypertension: a case–control study

A checkpoint on innate myeloid cells in pulmonary arterial hypertension

The genetics of pulmonary arterial hypertension in the post-BMPR2 era

United States Pulmonary Hypertension Scientific Registry (USPHSR): rationale, design, and clinical implications

Dysfunctional BMPR2 signaling drives an abnormal endothelial requirement for glutamine in pulmonary arterial hypertension

Impact of diabetes on survival and right ventricular compensation in pulmonary arterial hypertension

Pulmonary hypertension’s variegated landscape: a snapshot

Shared Gene Expression Patterns in Mesenchymal Progenitors Derived from Lung and Epidermis in Pulmonary Arterial Hypertension: Identifying Key Pathways in Pulmonary Vascular Disease

Shorter survival in familial versus idiopathic pulmonary arterial hypertension is associated with hemodynamic markers of impaired right ventricular function

Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression

Pulmonary hypertension's variegated landscape: a snapshot

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