Time of onset of atrial fibrillation and atrial fibrillation progression data from the RACE V study.

Autor: Lande, Martijn E van de, Rama, Rajiv S, Koldenhof, Tim, Arita, Vicente Artola, Nguyen, Bao-Oanh, Deutekom, Colinda van, Weberndorfer, Vanessa, Crijns, Harry J G M, Hemels, Martin E W, Tieleman, Robert G, Melis, Mirko de, Schotten, Ulrich, Linz, Dominik, Gelder, Isabelle C Van, Rienstra, Michiel, Investigators, for the RACE V

Publikováno v: EP: Europace; May2023, Vol. 25 Issue 5, p1-8, 8p

Temporal patterns and short-term progression of paroxysmal atrial fibrillation: data from RACE V

Autor: Ulrich Schotten, Hugo ten Cate, Bao-Oanh Nguyen, Michiel Rienstra, Isabelle C. Van Gelder, Arif Elvan, Race V Investigators, Mirko De Melis, Alexander H. Maass, Joris R de Groot, Martin E.W. Hemels, Abraham A. Kroon, Harry J.G.M. Crijns, Coert O S Scheerder, Henri M. H. Spronk, Justin G.L.M. Luermans, Ömer Erküner, Dominik Linz, Yuri Blaauw, Frank W J Körver, Robert G. Tieleman, Meelad I H Al-Jazairi

Publikováno v: Europace, 22, 1162-72
Europace
Europace, 22, 8, pp. 1162-72
EP Europace, 22(8), 1162-1172. Oxford University Press

Aims Atrial fibrillation (AF) often starts as a paroxysmal self-terminating arrhythmia. Limited information is available on AF patterns and episode duration of paroxysmal AF. In paroxysmal AF patients, we longitudinally studied the temporal AF patter

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73060f74239771649c2cd732afab2d5
http://hdl.handle.net/2066/225394

DPM2-CDG: A muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy

Autor: Barone, RITA MARIA ELISA, Aiello, C, Race, V, Morava, E, Foulquier, F, Riemersma, M, Passarelli, C, Concolino, D, Carella, M, Santorelli, F, Vleugels, W, Mercuri, E, Garozzo, Domenico, Sturiale, L, Messina, S, Jaeken, J, Fiumara, Agata, Wevers, Ra, Bertini, E, Matthijs, G, 2012 Oct, Lefeber D. J. Ann N. e. u. r. o. l., 72:550, 8.

Publikováno v: Annals of Neurology, 72, 550-8
Annals of neurology 72 (2012): 550–558. doi:10.1002/ana.23632
info:cnr-pdr/source/autori:R.Barone, Ch.Aiello, V.Race, E.Morava, F.Foulquier, M.Riemersma, Ch.Passarelli, D.Concolino, M.Carella, F.Santorelli, W.Vleugels, E.Mercuri, D.Garozzo, L.Sturiale, S.Messina, J.Jaeken, A.Fiumara, R.A.Wevers, E.Bertini, G.Matthijs, D. J.Lefeber/titolo:DPM2-CDG: A Muscular Dystrophy-Dystroglycanopathy Syndrome with Severe Epilepsy/doi:10.1002%2Fana.23632/rivista:Annals of neurology/anno:2012/pagina_da:550/pagina_a:558/intervallo_pagine:550–558/volume:72
Annals of Neurology, 72, 4, pp. 550-8

Item does not contain fulltext OBJECTIVE: Congenital disorders of glycosylation (CDG) are a group of metabolic diseases due to defects in protein and lipid glycosylation. We searched for the primary defect in 3 children from 2 families with a severe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82f8f06d840958b8a38d6b1ac4c27275
https://doi.org/10.1002/ana.23632

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