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The Left Ventricle in Congenital Diaphragmatic Hernia: Implications for the Management of Pulmonary Hypertension

The Journal of pediatrics, 2018-06, Vol.197, p.17-22

2018

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Type I interferon activation and endothelial dysfunction in caveolin-1 insufficiency-associated pulmonary arterial hypertension

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (11), p.1

2021

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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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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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Quantifying the impact of post‐acute sequelae of coronavirus on the cardiopulmonary endurance of athletes

Pulmonary circulation, 2024-07, Vol.14 (3), p.e12413-n/a

2024

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

Pulmonary circulation, 2022-07, Vol.12 (3), p.e12100-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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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-n/a

2023

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Deconstructing the Melting Pot in Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2020-06, Vol.201 (11), p.1329-1331

2020

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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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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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BMPR2 expression is suppressed by signaling through the estrogen receptor

Biology of sex differences, 2012-02, Vol.3 (1), p.6-6

2012

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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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Recent Advances in Pediatric Pulmonary Hypertension: Implications for Diagnosis and Treatment

Clinical therapeutics, 2023-09, Vol.45 (9), p.901-912

2023

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TBX4 syndrome: a systemic disease highlighted by pulmonary arterial hypertension in its most severe form

The European respiratory journal, 2020-05, Vol.55 (5), p.2000585

2020

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Expression of a Human Caveolin-1 Mutation in Mice Drives Inflammatory and Metabolic Defect-Associated Pulmonary Arterial Hypertension

Frontiers in medicine, 2020-09, Vol.7, p.540-540

2020

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The angiostatic peptide endostatin enhances mortality risk prediction in pulmonary arterial hypertension

ERJ open research, 2021-10, Vol.7 (4), p.378

2021

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COL18A1 genotypic associations with endostatin levels and clinical features in pulmonary arterial hypertension: a quantitative trait association study

ERJ open research, 2022-04, Vol.8 (2), p.725

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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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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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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Molecular Medicine of Pulmonary Arterial Hypertension: From Population Genetics to Precision Medicine and Gene Editing

American journal of respiratory and critical care medicine, 2017-01, Vol.195 (1), p.23

2017

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The Left Ventricle in Congenital Diaphragmatic Hernia: Implications for the Management of Pulmonary Hypertension

Type I interferon activation and endothelial dysfunction in caveolin-1 insufficiency-associated pulmonary arterial hypertension

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

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

Quantifying the impact of post‐acute sequelae of coronavirus on the cardiopulmonary endurance of athletes

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

Liver abnormalities in pulmonary arterial hypertension

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

Deconstructing the Melting Pot in Pulmonary Arterial Hypertension

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

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

Gender, sex hormones and pulmonary hypertension

BMPR2 expression is suppressed by signaling through the estrogen receptor

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

Recent Advances in Pediatric Pulmonary Hypertension: Implications for Diagnosis and Treatment

TBX4 syndrome: a systemic disease highlighted by pulmonary arterial hypertension in its most severe form

Expression of a Human Caveolin-1 Mutation in Mice Drives Inflammatory and Metabolic Defect-Associated Pulmonary Arterial Hypertension

The angiostatic peptide endostatin enhances mortality risk prediction in pulmonary arterial hypertension

COL18A1 genotypic associations with endostatin levels and clinical features in pulmonary arterial hypertension: a quantitative trait association study

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

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

Novel early life risk factors for adult pulmonary hypertension

Low-grade albuminuria in pulmonary arterial hypertension

Molecular Medicine of Pulmonary Arterial Hypertension: From Population Genetics to Precision Medicine and Gene Editing

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