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Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome

Autor: De Nittis P., Efthymiou S., Sarre A., Guex N., Chrast J., Putoux A., Sultan T., Raza Alvi J., Ur Rahman Z., Zafar F., Rana N., Rahman F., Anwar N., Maqbool S., Zaki M. S., Gleeson J. G., Murphy D., Galehdari H., Shariati G., Mazaheri N., Sedaghat A., Lesca G., Chatron N., Salpietro V., Christoforou M., Houlden H., Simonds W. F., Pedrazzini T., Maroofian R., Reymond A., SYNAPS STUDY GROUP: SYNAPS Study Group: Stanislav Groppa, Blagovesta Marinova Karashova, Wolfgang Nachbauer, Sylvia Boesch, Larissa Arning, Dagmar Timmann, Bru Cormand, Belen Pérez-Dueñas, Jatinder S Goraya, Tipu Sultan, Jun Mine, Daniela Avdjieva, Hadil Kathom, Radka Tincheva, Selina Banu, Mercedes Pineda-Marfa, Pierangelo Veggiotti, Michel D. Ferrari, Arn M. J. M. van den Maagdenberg, Alberto Verrotti, Giangluigi Marseglia, Salvatore Savasta, Mayte García-Silva, Alfons Macaya Ruiz, Barbara Garavaglia, Eugenia Borgione, Simona Portaro, Benigno Monteagudo Sanchez, Richard Boles, Savvas Papacostas, Michail Vikelis, Eleni Zamba Papanicolaou, Efthymios Dardiotis, Shazia Maqbool, Shahnaz Ibrahim, Salman Kirmani, Nuzhat Noureen Rana, Osama Atawneh, George Koutsis, Salvatore Mangano, Carmela Scuderi, Giovanna Morello, Tanya Stojkovic, Massimo Zollo, Gali Heimer, Yves A. Dauvilliers, Pasquale Striano, Issam Al-Khawaja, Fuad Al-Mutairi, Hamed Sherifa.

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, In press, ⟨10.1136/jmedgenet-2020-107015⟩

BackgroundPathogenic variants of GNB5 encoding the β5 subunit of the guanine nucleotide-binding protein cause IDDCA syndrome, an autosomal recessive neurodevelopmental disorder associated with cognitive disability and cardiac arrhythmia, particularl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c9ebc9c3b81e32161c102409b0091df
https://doi.org/10.1136/jmedgenet-2020-107015

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The continuous heart failure spectrum: Moving beyond an ejection fraction classification

Autor: Triposkiadis, F. Butler, J. Abboud, F.M. Armstrong, P.W. Adamopoulos, S. Atherton, J.J. Backs, J. Bauersachs, J. Burkhoff, D. Bonow, R.O. Chopra, V.K. De Boer, R.A. De Windt, L. Hamdani, N. Hasenfuss, G. Heymans, S. Hulot, J.-S. Konstam, M. Lee, R.T. Linke, W.A. Lunde, I.G. Lyon, A.R. Maack, C. Mann, D.L. Mebazaa, A. Mentz, R.J. Nihoyannopoulos, P. Papp, Z. Parissis, J. Pedrazzini, T. Rosano, G. Rouleau, J. Seferovic, P.M. Shah, A.M. Starling, R.C. Tocchetti, C.G. Trochu, J.-N. Thum, T. Zannad, F. Brutsaert, D.L. Segers, V.F. De Keulenaer, G.W.

Randomized clinical trials initially used heart failure (HF) patients with low left ventricular ejection fraction (LVEF) to select study populations with high risk to enhance statistical power. However, this use of LVEF in clinical trials has led to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::fdaec79e01b2d2efd782ad51e0c68d22
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105822

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