Differences in phyisical activity level between the congenital heart disease associated PAH and idiopathic

Autor: SAVCI, SEMA, SEVİNÇ, CAN, ACAR, SERAP, ÖZPELİT, EBRU, KARADİBAK, DİDEM, ÖZCAN KAHRAMAN, BUSE, AKDENİZ, BAHRİ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2605::3d8b4b2ea22188114eb34c9d0853cc5b
https://avesis.deu.edu.tr/publication/details/26c9ee8b-a14e-4922-afdc-a872c3d6c45e/oai

Differences In Physical Activity Level Between The Congenital Heart Disease Associated PAH And Idiopathic PAH

Autor: Can Sevinc, Bahri Akdeniz, Didem Karadibak, Sema Savc, Serap Acar, Buse Ozcan, Ebru Özpelit

Publikováno v: Medicine & Science in Sports & Exercise. 47:635

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ff0c3548c56887a3ef2efbc8d7fc2a4b
https://doi.org/10.1249/01.mss.0000478449.30169.b7

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Defining the clinical validity of genes reported to cause pulmonary arterial hypertension

Autor: Callejo, Emily P. ¹, Day, Kristina M. ², Macaya, Daniela ³, Maldonado-Velez, Gabriel ², Archer, Stephen L. ¹, Auckland, Kathryn ², Austin, Eric D. ³, Badagliacca, Roberto ⁴, Barberà, Joan-Albert ⁵, Belge, Catharina ⁶, Bogaard, Harm Jan ⁷, Bonnet, Sébastien ^{8, 9}, Boomars, Karin A. ¹⁰, Boucherat, Olivier ^{9, 11}, Chakinala, Murali M. ¹², Condliffe, Robin ^{13, 14}, Damico, Rachel Lynn ¹⁵, Delcroix, Marion ¹⁶, Desai, Ankit A. ¹⁷, Doboszynska, Anna ¹⁸, Elliott, C. Greg ¹⁹, Eyries, Melanie ^{20, 21}, Escribano Subías, Maria Pilar ^{22, 23, 24, 25}, Gall, Henning ²⁶, Ghio, Stefano ²⁷, Ghofrani, Ardeschir-Hossein ^{26, 28}, Grünig, Ekkehard ²⁹, Hamid, Rizwan ³⁰, Harbaum, Lars ³¹, Hassoun, Paul M. ¹⁵, Hemnes, Anna R. ³², Hinderhofer, Katrin ³³, Howard, Luke S. ³¹, Humbert, Marc ^{34, 35, 36}, Kiely, David G. ³⁷, Langleben, David ³⁸, Lawrie, Allan ¹³, Loyd, Jim E. ³⁹, Moledina, Shahin ⁴⁰, Montani, David ^{35, 41}, Morrell, Nichols W. ^{42, 43}, Nichols, William C. ⁴⁴, Olschewski, Andrea ⁴⁵, Olschewski, Horst ^{45, 46}, Papa, Silvia ⁴, Pauciulo, Mike W. ⁴⁴, Provencher, Steve ^{9, 11}, Quarck, Rozenn ⁶, Rhodes, Christopher J. ³¹, Scelsi, Laura ²⁸, Seeger, Werner ²⁷, Stewart, Duncan J. ⁴⁵, Sweatt, Andrew ⁴⁶, Swietlik, Emilia M. ⁴², Treacy, Carmen ², Trembath, Richard C. ⁴⁷, Tura-Ceide, Olga ^{48, 49, 50}, Vizza, Carmine Dario ⁴, Vonk Noordegraaf, Anton ⁵¹, Wilkins, Martin R. ³¹, Zamanian, Roham T. ⁵², Zateyshchikov, Dmitry ⁵³, Welch, Carrie L. ¹, Aldred, Micheala A. ², Balachandar, Srimmitha ², Dooijes, Dennis ³, Eichstaedt, Christina A. ^{4, 5}, Gräf, Stefan ^{6, 7}, Houweling, Arjan C. ⁸, Machado, Rajiv D. ⁹, Pandya, Divya ⁷, Prapa, Matina ^{7, 10}, Shaukat, Memoona ^{4, 5}, Southgate, Laura ⁹, Tenorio-Castano, Jair ^{11, 12, 13}, Chung, Wendy K. ^{1, 14, ∗}

Publikováno v: In Genetics in Medicine November 2023 25(11)

The BMPR2, ALK1 and ENG Genes Mutation in Congenital Heart DiseaseAssociated Pulmonary Artery Hypertension

Autor: Hartopo, Anggoro Budi, Anggrahini, Dyah Wulan, Emoto, Noriaki, Dinarti, Lucia Kris

Publikováno v: ACI (Acta Cardiologia Indonesiana); Vol 5, No 2 (2019); 145-149

The gene mutation is one of the background underlie the pathogenesis of pulmonary artery hypertension (PAH). Several genes have been recognized to be responsible for the development of PAH. The mutation in transforming growth factor-β (TGF-β) pathw

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jurnalonline::f30ad733143a913081c1f4f3876293a9
https://journal.ugm.ac.id/jaci/article/view/50222