Search Results - "Ochoa Parra, Nuria"

Description of Two New Cases of AQP1 Related Pulmonary Arterial Hypertension and Review of the Literature by Gallego-Zazo, Natalia, Cruz-Utrilla, Alejandro, Del Cerro, María Jesús, Ochoa Parra, Nuria, Blanco, Julián Nevado, Arias, Pedro, Lapunzina, Pablo, Escribano-Subias, Pilar, Tenorio-Castaño, Jair

“…Pulmonary arterial hypertension (PAH) is a severe clinical condition characterized by an increase in mean pulmonary artery pressure, which leads to a right…”
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Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary Arterial Hypertension by Castaño, Jair Antonio Tenorio, Hernández-Gonzalez, Ignacio, Gallego, Natalia, Pérez-Olivares, Carmen, Ochoa Parra, Nuria, Arias, Pedro, Granda, Elena, Acebo, Gonzalo Gómez, Lago-Docampo, Mauro, Palomino-Doza, Julian, López Meseguer, Manuel, del Cerro, María Jesús, PAH Consortium, Spanish, Valverde, Diana, Lapunzina, Pablo, Escribano-Subías, Pilar

“…Pulmonary arterial hypertension is a very infrequent disease, with a variable etiology and clinical expressivity, making sometimes the clinical diagnosis a…”
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Seven Additional Patients with SOX17 Related Pulmonary Arterial Hypertension and Review of the Literature by Gallego-Zazo, Natalia, Miranda-Alcaraz, Lucía, Cruz-Utrilla, Alejandro, Del Cerro Marín, María Jesús, Álvarez-Fuente, María, Del Mar Rodríguez Vázquez Del Rey, María, Guillén Rodríguez, Inmaculada, Becerra-Munoz, Victor Manuel, Moya-Bonora, Amparo, Ochoa Parra, Nuria, Parra, Alejandro, Pascual, Patricia, Cazalla, Mario, Silván, Cristina, Arias, Pedro, Valverde, Diana, de Jesús-Pérez, Vinicio, Lapunzina, Pablo, Escribano-Subías, Pilar, Tenorio-Castano, Jair

“…Pulmonary arterial hypertension (PAH) is an infrequent disorder characterized by high blood pressure in the pulmonary arteries. It may lead to premature death…”
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Novel Genetic and Molecular Pathways in Pulmonary Arterial Hypertension Associated with Connective Tissue Disease by Hernandez-Gonzalez, Ignacio, Tenorio-Castano, Jair, Ochoa-Parra, Nuria, Gallego, Natalia, Pérez-Olivares, Carmen, Lago-Docampo, Mauro, Palomino Doza, Julian, Valverde, Diana, Lapunzina, Pablo, Escribano-Subias, Pilar

“…Pulmonary Arterial Hypertension (PAH) is a severe complication of Connective Tissue Disease (CTD), with remarkable morbidity and mortality. However, the…”
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Assessing the clinical benefit, safety, and patient-reported outcomes with the use of the PAHcare™ digital platform in pulmonary arterial hypertension: a pilot study by Peñate, Gregorio Pérez, Parra, Nuria Ochoa, Morera, Juan Antonio Domingo, Meñaca, Amaya Martínez, Ramón, Marta López, Menéndez, Sergio Cadenas, Marrero, Fernando León, de la Cal, Sara Gómara, Ghadban-Garrido, Cristina, Tolosana, Patricia Royo, Puentes, Javier Martín, Aguayo, Rebeca Aldonza, Mahdavi, Hadis, Jeanneret, Gabriela Bacchini, Subías, Pilar Escribano

“…Digital health interventions, particularly mobile health platforms, have shown promise in supporting patients with respiratory conditions, but their…”
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Evaluation of a digital health system (PAHcare™) for routine care of patients with pulmonary arterial hypertension: The CBS-PAH study protocol by Pérez Peñate, Gregorio, Ochoa Parra, Nuria, Domingo Morera, Juan Antonio, Martínez Meñaca, Amaya, López Ramón, Marta, Cadenas Menéndez, Sergio, León Marrero, Fernando, Gómara de la Cal, Sara, Ghadban Garrido, Cristina, Royo Tolosana, Patricia, Martin Puentes, Javier, Aldonza Aguayo, Rebeca, Mahdavi, Hadis, Bacchini Jeanneret, Gabriela, Escribano Subías, Pilar

“…Pulmonary arterial hypertension (PAH) is a rare, multifactorial, chronic condition that requires ongoing monitoring and assessment. PAHcare™ is a novel,…”
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Inoperable chronic thromboembolic pulmonary hypertension treated with riociguat: A case study by Ortiz-Bautista, Carlos, Ochoa-Parra, Nuria, Navas-Tejedor, Paula, Morán-Fernández, Laura, Gómez-Sánchez, Miguel Ángel

“…A 51-year-old woman presented with a one-year history of progressive dyspnea, WHO functional class III-IV and exercise-related syncope. Transthoracic…”
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Genetic counselling and testing in pulmonary arterial hypertension: a consensus statement on behalf of the International Consortium for Genetic Studies in PAH by Eichstaedt, Christina A, Belge, Catharina, Chung, Wendy K, Gräf, Stefan, Grünig, Ekkehard, Montani, David, Quarck, Rozenn, Tenorio-Castano, Jair A, Soubrier, Florent, Trembath, Richard C, Morrell, Nicholas W

“…Pulmonary arterial hypertension (PAH) is a rare disease that can be caused by (likely) pathogenic germline genomic variants. In addition to the most prevalent…”
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Seven Additional Patients with ISOX17/I Related Pulmonary Arterial Hypertension and Review of the Literature by Gallego-Zazo, Natalia, Miranda-Alcaraz, Lucía, Cruz-Utrilla, Alejandro, del Cerro Marín, María Jesús, Álvarez-Fuente, María, del Mar Rodríguez Vázquez del Rey, María, Guillén Rodríguez, Inmaculada, Becerra-Munoz, Victor Manuel, Moya-Bonora, Amparo, Ochoa Parra, Nuria, Parra, Alejandro, Pascual, Patricia, Cazalla, Mario, Silván, Cristina, Arias, Pedro, Valverde, Diana, de Jesús-Pérez, Vinicio, Lapunzina, Pablo, Escribano-Subías, Pilar, Tenorio-Castano, Jair

“…Pulmonary arterial hypertension (PAH) is an infrequent disorder characterized by high blood pressure in the pulmonary arteries. It may lead to premature death…”
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Usefulness of genetics for clinical reclassification and refinement of prognostic stratification in pulmonary arterial hypertension by Cruz-Utrilla, Alejandro, Gallego-Zazo, Natalia, Pérez-Olivares, Carmen, Hernández-González, Ignacio, Bedate, Pedro, Martínez Meñaca, Amaya, López Meseguer, Manuel, Lapunzina, Pablo, Pérez Núñez, Marta, Ochoa Parra, Nuria, Valverde, Diana, Tenorio-Castaño, Jair Antonio, Escribano-Subias, Pilar

“…Risk stratification in pulmonary arterial hypertension (PAH) is essential to provide more aggressive treatment for patients at higher risk. Nevertheless,…”
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Utilidad de la genética en la reclasificación y la mejoría en la estratificación pronóstica en la hipertensión arterial pulmonar by Cruz-Utrilla, Alejandro, Gallego-Zazo, Natalia, Pérez-Olivares, Carmen, Hernández-González, Ignacio, Bedate, Pedro, Martínez Meñaca, Amaya, López Meseguer, Manuel, Lapunzina, Pablo, Pérez Núñez, Marta, Ochoa Parra, Nuria, Valverde, Diana, Tenorio-Castaño, Jair Antonio, Escribano-Subias, Pilar

“…La evaluación del riesgo en la hipertensión arterial pulmonar (HAP) es esencial de cara a administrar un tratamiento más agresivo a aquellos pacientes de mayor…”
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