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Philippe Chouvarine

Explore the profile of Philippe Chouvarine including associated specialties, affiliations and a list of published articles. Areas
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Articles 42
Citations 718
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Recent Articles
1.
Legchenko E, Chouvarine P, Hysko K, Qadri F, Wesolowski R, Specker E, et al.
Am J Respir Cell Mol Biol . 2025 Feb; PMID: 39899532
Inhaled pharmacotherapies are promising treatment options for patients with pulmonary arterial hypertension (PAH) as they minimize extrapulmonary adverse effects. Recently, we developed a highly specific inhibitor (TPHi) of the serotonin...
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Hansmann G, Chouvarine P, Diekmann F, Giera M, Ralser M, Mulleder M, et al.
Nat Cardiovasc Res . 2024 Aug; 1(6):568-576. PMID: 39195868
Here we report application of human umbilical cord mesenchymal stem cell (HUCMSC)-derived therapy for pulmonary arterial hypertension (PAH). A 3-year-old female presented with heritable PAH associated with hereditary hemorrhagic telangiectasia...
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Legchenko E, Chouvarine P, Qadri F, Specker E, Nazare M, Wesolowski R, et al.
JACC Basic Transl Sci . 2024 Aug; 9(7):890-902. PMID: 39170954
The serotonin pathway has long been proposed as a promising target for pulmonary arterial hypertension (PAH)-a progressive and uncurable disease. We developed a highly specific inhibitor of the serotonin synthesizing...
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Hasan H, Chouvarine P, Hansmann G
JACC Adv . 2024 Jun; 1(3):100055. PMID: 38938394
No abstract available.
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Beder T, Hansen B, Hartmann A, Zimmermann J, Amelunxen E, Wolgast N, et al.
Hemasphere . 2023 Aug; 7(9):e939. PMID: 37645423
Current classifications (World Health Organization-HAEM5/ICC) define up to 26 molecular B-cell precursor acute lymphoblastic leukemia (BCP-ALL) disease subtypes by genomic driver aberrations and corresponding gene expression signatures. Identification of driver...
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Jack T, Carlens J, Diekmann F, Hasan H, Chouvarine P, Schwerk N, et al.
Front Cardiovasc Med . 2023 Jul; 10:1193326. PMID: 37441704
Background: Bilateral lung transplantation (LuTx) remains the only established treatment for children with end-stage pulmonary arterial hypertension (PAH). Although PAH is the second most common indication for LuTx, little is...
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Schweintzger S, Kurath-Koller S, Burmas A, Grangl G, Fandl A, Noessler N, et al.
Front Cardiovasc Med . 2022 Aug; 9:950765. PMID: 35911557
Background: An accurate assessment of the right and left ventricle and their interaction is important in pediatric pulmonary hypertension (PH). Our objective was to provide normal reference values for the...
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Hasan H, Chouvarine P, Diekmann F, Diedrich N, Koestenberger M, Hansmann G
Eur J Clin Invest . 2022 Jul; 52(11):e13835. PMID: 35844040
Objectives: In 2019, the European Paediatric Pulmonary Vascular Disease Network (EPPVDN) developed a PH risk score to assess the risk and severity of pulmonary hypertension (PH) in children and young...