Results 31 to 40 of about 1,381,406 (265)

Differences in health policies for drug availability in pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension across Latin America

Pulmonary Circulation, 2022
Treatment for pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension in Latin America differs between countries, with regard to disease etiology, health insurance coverage, and drug availability.
Mauricio Orozco‐Levi, Jorge Cáneva, Caio Fernandes, Ricardo Restrepo‐Jaramillo, Nayeli Zayas, Rafael Conde, Mirta Diez, Carlos Jardim, Manuel C. Pacheco Gallego, Luciano Melatini, Héctor Valdéz, Tomás Pulido   +11 more
doaj   +1 more source

Intravenous iron therapy in patients with idiopathic pulmonary arterial hypertension and iron deficiency. [PDF]

, 2015
In patients with idiopathic pulmonary arterial hypertension (iPAH), iron deficiency is common and has been associated with reduced exercise capacity and worse survival. Previous studies have shown beneficial effects of intravenous iron administration. In
Ruiter, G, van der Laarse, W.J., Howard, LS, Vonk‐Noordegraaf Anton, Chris M. Happé, Happe, C.M., Luke S. Howard, Westerhof, N, Schalij, I, Howard, L.S., Wilkins, MR, Emmy Manders, Ruiter, G., van der Laarse, WJ, Westerhof, N., Schalij, I., Manders, E, Happé, CM, Harm J. Bogaard, Bogaard, HJ, de Man, FS, Wilkins, M.R., Groepenhoff, H, Bogaard, H.J., de Man, F.S., Gerrina Ruiter, Herman Groepenhoff, Frances S. de Man, Vonk-Noordegraaf, A, Vonk-Noordegraaf, A., Willem J. van der Laarse, Ingrid Schalij, Manders, E., Groepenhoff, H., Nico Westerhof, Martin R. Wilkins   +35 more
core   +1 more source

Diagnostic tools in pulmonary arterial hypertension management

, 2010
An accurate differential diagnosis is crucial in pulmonary hypertension/pulmonary arterial hypertension (PH/PAH), because the treatment options in the different PH/PAH groups and subgroups differ substantially.
Vonk Noordegraaf, Anton, Heinrike Wilkens, Vonk-Noordegraaf, Anton, Wilkens, Heinrike, Anton Vonk Noordegraaf, Robert Naeije, Naeije, Robert   +6 more
core   +1 more source

Right heart adaptation to pulmonary arterial hypertension: physiology and pathobiology. [PDF]

, 2013
Survival in patients with pulmonary arterial hypertension (PAH) is closely related to right ventricular (RV) function. Although pulmonary load is an important determinant of RV systolic function in PAH, there remains a significant variability in RV ...
Voelkel, N.F., Kawut, Steven M, Forfia, Paul R, Voelkel, Norbert F, Provencher, Steve, Oudiz, Ronald J, Haddad, F., Kawut, S.M., Newman, J., Kawut, Steven M., Naeije, R., Hassoun, P.M., Chin, Kelly M, Lumens, Joost, Forfia, Paul R., Newman, John, Voelkel, Norbert F., Forfia, P.R., Vonk-Noordegraaf, Anton, Lumens, Joost; id_orcid, Oudiz, Ronald J., Chin, K.M., Hassoun, Paul M, Torbicki, Adam, Oudiz, R.J., Hassoun, Paul M., Vonk-Noordegraaf, A., Torbicki, A., Chin, Kelly M., Provencher, S., Lumens, J., Haddad, François, Naeije, Robert   +32 more
core   +1 more source

RhoA activation by hypoxia in pulmonary arterial smooth muscle cells is age and site specific [PDF]

, 2004
Hypoxia induces vasoconstriction of pulmonary arteries through contraction of smooth muscle cells (SMCs). The GTPase RhoA regulates smooth muscle contractility and actin cytoskeletal remodeling through the Rho-associated kinase ( ROCK).
Bailly, K, Ridley, A J, Haworth, SG, Ridley, AJ, Hall, SM, Hall, S M, Haworth, S G   +6 more
core   +1 more source

Pulmonary hypertension

, 2016
In 2015, more than 800 papers were published in the field of pulmonary hypertension. A Clinical Year in Review article cannot possibly incorporate all this work and needs to be selective.
Harm Jan Bogaard, Bogaard, Harm Jan, Vonk Noordegraaf, Anton, Groeneveldt, Joanne A., Noordegraaf, Anton Vonk, Joanne A. Groeneveldt, Anton Vonk Noordegraaf   +6 more
core   +1 more source

Genetic counselling for pulmonary arterial hypertension: a matter of variable variability [PDF]

, 2011
We report three cases which highlight the complex considerations surrounding genetic counselling for pulmonary arterial hypertension (PAH). The first counselee developed PAH symptoms shortly after his daughter's death from PAH and was diagnosed with a ...
A. Vonk Noordegraaf, F. B. Postma, Meijers-Heijboer, E. J., Vonk Noordegraaf, A., A. B. Boonstra, J. J. P. Gille, Boonstra, A. B., Gille, J.J.P., Leter, E. M., Leter, E.M., Postma, F. B., Meijers-Heijboer, E.J., Postma, F., E. J. Meijers-Heijboer, E. M. Leter, Boonstra, A., Gille, J. J. P.   +16 more
core   +2 more sources

Influenza Vaccination Responses in Disabled Stroke Patients: A Single‐Center Prospective Observational Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective This study aimed to investigate the immunological response to influenza vaccination, the incidence and severity of influenza infection, and the side effects of the vaccination in patients with ischemic stroke. Methods This prospective observational study was conducted between 2023 and 2024 at Ramathibodi Hospital.
Achiraya Pakngao, Sureerat Suwatcharangoon, Pintip Ngamjanyapron, Kobporn Boonnak, Thanitta Suangtamai, Porpon Rotjanapan   +5 more
wiley   +1 more source

Pulmonary hypertension associated with neurofibromatosis type 2

Pulmonary Circulation, 2021
Although precapillary pulmonary hypertension is a rare but severe complication of patients with neurofibromatosis type 1 (NF1), its association with NF2 remains unknown.
Hirohisa Taniguchi, Tomoya Takashima, Ly Tu, Raphaël Thuillet, Asuka Furukawa, Yoshiko Furukawa, Akio Kawamura, Marc Humbert, Christophe Guignabert, Yuichi Tamura   +9 more
doaj   +1 more source

Definitions and Diagnosis of Pulmonary Hypertension [PDF]

, 2013
Pulmonary hypertension (PH) is defined by a mean pulmonary artery pressure ≥25 mm Hg at rest, measured during right heart catheterization. There is still insufficient evidence to add an exercise criterion to this definition.
Satoh, T., Bogaard, Harm Jan, Kurzyna, M., Wilkins, M.R., Frantz, R., Langleben, David, Khanna, Dinesh, Manes, Alessandra, Bogaard, H.J., Khanna, D., Badesch, David B., Hoeper, Marius M., Kurzyna, Marcin, Torres, F., Hoeper, M.M., Satoh, Toru, Wilkins, Martin R., Torres, Fernando, Condliffe, R., Langleben, D., Badesch, D.B., Frantz, Robert, Condliffe, Robin, Manes, A.   +23 more
core   +1 more source