Zobrazeno 1 - 10 of 63 pro vyhledávání: '"Ahmad S Amin"'
1
Cardiac Repolarization in Health and Disease
Autor: Christian Krijger Juárez, Ahmad S. Amin, Joost A. Offerhaus, Connie R. Bezzina, Bastiaan J. Boukens
Publikováno v: JACC: Clinical Electrophysiology. 9:124-138
Abnormal cardiac repolarization is at the basis of life-threatening arrhythmias in various congenital and acquired cardiac diseases. Dysfunction of ion channels involved in repolarization at the cellular level are often the underlying cause of the re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdb220f0ed52d30523cd5cbaf3ae1be1
https://doi.org/10.1016/j.jacep.2022.09.017
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2
Multimodality Screening For (Peri)Myocarditis In Newly Diagnosed Idiopathic Inflammatory Myopathies
Autor: Johan Lim, Hannah A.W. Walter, Rianne A.C.M. de Bruin-Bon, Myrthe C. Jarings, R. Nils Planken, Wouter E.M. Kok, Joost Raaphorst, Yigal M. Pinto, Ahmad S. Amin, S. Matthijs Boekholdt, Anneke J. van der Kooi
Publikováno v: Journal of neuromuscular diseases, 10(2), 185-197. IOS Press
Lim, J, Walter, H A W, de Bruin-Bon, R A C M, Jarings, M C, Planken, R N, Kok, W E M, Raaphorst, J, Pinto, Y M, Amin, A S, Boekholdt, S M & van der Kooi, A J 2023, ' Multimodality Screening For (Peri)Myocarditis In Newly Diagnosed Idiopathic Inflammatory Myopathies : A Cross-Sectional Study ', Journal of Neuromuscular Diseases, vol. 10, no. 2, pp. 185-197 . https://doi.org/10.3233/JND-221582
Journal of Neuromuscular Diseases, 10(2), 185-197. Elsevier Limited
Background: Cardiac involvement in idiopathic inflammatory myopathy (IIM or “myositis”) is associated with an approximate 4% mortality, but standardised screening strategies are lacking. Objective: We explored a multimodality screening on potenti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::543c7008d3344b646dbd060894c78bba
https://doi.org/10.3233/jnd-221582
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3
Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy
Autor: Steven A. Muller, Alessio Gasperetti, Laurens P. Bosman, Amand F. Schmidt, Annette F. Baas, Ahmad S. Amin, Arjan C. Houweling, Arthur A.M. Wilde, Paolo Compagnucci, Mattia Targetti, Michela Casella, Leonardo Calò, Claudio Tondo, Pim van der Harst, Folkert W. Asselbergs, J. Peter van Tintelen, Marish I.F.J. Oerlemans, Anneline S.J.M. Te Riele
Publikováno v: Muller, S A, Gasperetti, A, Bosman, L P, Schmidt, A F, Baas, A F, Amin, A S, Houweling, A C, Wilde, A A M, Compagnucci, P, Targetti, M, Casella, M, Calò, L, Tondo, C, van der Harst, P, Asselbergs, F W, van Tintelen, J P, Oerlemans, M I F J & te Riele, A S J M 2023, ' Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy ', Journal of the American College of Cardiology, vol. 82, no. 3, pp. 214-225 . https://doi.org/10.1016/j.jacc.2023.05.005
Background: Clinical guidelines recommend regular screening for arrhythmogenic right ventricular cardiomyopathy (ARVC) to monitor at-risk relatives, resulting in a significant burden on clinical resources. Prioritizing relatives on their probability
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19a3a6c4d50d4019c6c8af625c973480
https://doi.org/10.1016/j.jacc.2023.05.005
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4
Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity?
Autor: Saskia N. van der Crabben, Stellan Mörner, Anna C. Lundström, Jenni Jonasson, Hennie Bikker, Ahmad S. Amin, Annika Rydberg, Arthur A. M. Wilde
Publikováno v: van der Crabben, S N, Mörner, S, Lundström, A C, Jonasson, J, Bikker, H, Amin, A S, Rydberg, A & Wilde, A A M 2022, ' Should variants of unknown significance (VUS) be disclosed to patients in cardiogenetics or not; only in case of high suspicion of pathogenicity? ', European Journal of Human Genetics, vol. 30, no. 11, pp. 1208-1210 . https://doi.org/10.1038/s41431-022-01173-z
European journal of human genetics, 30(11), 1208-1210. Nature Publishing Group
European Journal of Human Genetics, 30(11), 1208-1210. Nature Publishing Group
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa4015b6489c8399c8d1ee3808e327b
https://doi.org/10.1038/s41431-022-01173-z
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5
Akademický článek
Disease Modifiers of Inherited SCN5A Channelopathy
Autor: Arie O. Verkerk, Ahmad S. Amin, Carol Ann Remme
Publikováno v: Frontiers in Cardiovascular Medicine, Vol 5 (2018)
To date, a large number of mutations in SCN5A, the gene encoding the pore-forming α-subunit of the primary cardiac Na+ channel (NaV1.5), have been found in patients presenting with a wide range of ECG abnormalities and cardiac syndromes. Although th
Externí odkaz: https://doaj.org/article/67d16f4fadbf4c5991e83ad9a738252c
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6
The β-angle can help guide clinical decisions in the diagnostic work-up of patients suspected of Brugada syndrome
Autor: Arthur A.M. Wilde, Jeroen Vendrik, Hanno L. Tan, Jan A. Kors, Pieter G. Postema, Tom E Verstraelen, Ahmad S. Amin, Martijn H. van der Ree
Publikováno v: Europace
Europace, 23(12), 2020-2028. Oxford University Press
EP Europace
Aims In patients with Brugada syndrome (BrS) but without spontaneous Type-1 electrocardiogram, several electrocardiographic characteristics have been studied, including the β-angle. Previous studies suggested that the β-angle might be useful in dis
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c93c08b852c2959cbea38fbcbdbd5dcd
https://doi.org/10.1093/europace/euab128
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7
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
Autor: Edgar T. Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N. Parikh, Gerard J. te Meerman, Belinda Gray, Ahmet Adiyaman, Richard D. Bagnall, Daniela Q.C.M. Barge-Schaapveld, Maarten P. van den Berg, Marianne Bootsma, Laurens P. Bosman, Gemma Correnti, Johan Duflou, Ruben N. Eppinga, Diane Fatkin, Michael Fietz, Eric Haan, Jan D.H. Jongbloed, Arnaud D. Hauer, Lien Lam, Freyja H.M. van Lint, Amrit Lota, Carlo Marcelis, Hugh J. McCarthy, Anneke M. van Mil, Rogier A. Oldenburg, Nicholas Pachter, R. Nils Planken, Chloe Reuter, Christopher Semsarian, Jasper J. van der Smagt, Tina Thompson, Jitendra Vohra, Paul G.A. Volders, Jaap I. van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S. Amin, Arthur A.M. Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A. Ashley, Matthew T. Wheeler, James S. Ware, J. Peter van Tintelen, Jodie Ingles
Publikováno v: Circulation. Genomic and Precision Medicine, 16, 1
Circulation: Genomic and Precision Medicine, 16(1):E003672. LIPPINCOTT WILLIAMS & WILKINS
Circulation. Genomic and precision medicine, 16(1). Lippincott Williams and Wilkins Ltd.
Circulation: Genomic and Precision Medicine, 16(1), 69-79. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and Precision Medicine, 16
Circulation: Genomic and Precision Medicine, 16(1). Lippincott Williams & Wilkins
Background: Truncating variants in desmoplakin ( DSP tv) are an important cause of arrhythmogenic cardiomyopathy; however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors fo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168e6f2d791aa1fd96556c202c710360
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10
Diagnosis, management and therapeutic strategies for congenital long QT syndrome
Autor: Pieter G Postema, Arthur A. M. Wilde, Ahmad S Amin
Publikováno v: Heart. 108:332-338
Congenital long QT syndrome (LQTS) is characterised by heart rate corrected QT interval prolongation and life-threatening arrhythmias, leading to syncope and sudden death. Variations in genes encoding for cardiac ion channels, accessory ion channel s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daa6a1a69bfdc6326ba79c0eceaadfd4
https://doi.org/10.1136/heartjnl-2020-318259
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