Items where Author is "Vohra, Jitendra"
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Hoorntje, Edgar T. and Burns, Charlotte and Marsili, Luisa and Corden, Ben and Parikh, Victoria N. and te Meerman, Gerard J. and Gray, Belinda and Adiyaman, Ahmet and Bagnall, Richard D. and Barge-Schaapveld, Daniela Q.C.M. and van den Berg, Maarten P. and Bootsma, Marianne and Bosman, Laurens P. and Correnti, Gemma and Duflou, Johan and Eppinga, Ruben N. and Fatkin, Diane and Fietz, Michael and Haan, Eric and Jongbloed, Jan D.H. and Hauer, Arnaud D. and Lam, Lien and van Lint, Freyja H.M. and Lota, Amrit and Marcelis, Carlo and McCarthy, Hugh J. and van Mil, Anneke M. and Oldenburg, Rogier A. and Pachter, Nicholas and Planken, R. Nils and Reuter, Chloe and Semsarian, Christopher and van der Smagt, Jasper J. and Thompson, Tina and Vohra, Jitendra and Volders, Paul G.A. and van Waning, Jaap I. and Whiffin, Nicola and van den Wijngaard, Arthur and Amin, Ahmad S. and Wilde, Arthur A.M. and van Woerden, Gijs and Yeates, Laura and Zentner, Dominica and Ashley, Euan A. and Wheeler, Matthew T. and Ware, James S. and van Tintelen, J. Peter and Ingles, Jodie (2023) Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation: Genomic and Precision Medicine, 16 (1). ISSN 2574-8300
Priori, Silvia G and Wilde, Arthur A and Horie, Minoru and Cho, Yongkeun and Behr, Elijah R and Berul, Charles and Blom, Nico and Brugada, Josep and Chiang, Chern-En and Huikuri, Heikki and Kannankeril, Prince and Krahn, Andrew and Leenhardt, Antoine and Moss, Arthur and Schwartz, Peter J and Shimizu, Wataru and Tomaselli, Gordon and Tracy, Cynthia and Ackerman, Michael and Belhassen, Bernard and Estes, N A Mark and Fatkin, Diane and Kalman, Jonathan and Kaufman, Elizabeth and Kirchhof, Paulus and Schulze-Bahr, Eric and Wolpert, Christian and Vohra, Jitendra and Refaat, Marwan and Etheridge, Susan P and Campbell, Robert M and Martin, Edward T and Quek, Swee Chye (2013) Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Europace, 15 (10). pp.1389-406. ISSN 1532-2092 (OA)