Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Joan Campagna"'
Autor:
Vasanth Vedantham, Rahul C. Deo, Joan Campagna, Martin S. Green, Michael H. Gollob, Nitish Badhwar, Julianne Wojciak, Jeffrey E. Olgin, George J. Klein, Charlie Young, Melvin M. Scheinman, Pui-Yan Kwok, Jason D. Roberts, Stephen B. Wilton, Dennis W.X. Zhu, Annie Poon, Gregory M. Marcus, Qiuju Li, Sean Connors, Anthony Tang, Kathleen A. Hodgkinson, Chris Gray, Nathan Orr
Publikováno v:
JACC: Clinical Electrophysiology. 3:276-288
Objectives This study sought to investigate for an underlying genetic etiology in cases of apparent idiopathic bundle branch re-entrant ventricular tachycardia (BBRVT). Background BBRVT is a life-threatening arrhythmia occurring secondary to macro–
Autor:
Jason D, Roberts, Michael H, Gollob, Charlie, Young, Sean P, Connors, Chris, Gray, Stephen B, Wilton, Martin S, Green, Dennis W, Zhu, Kathleen A, Hodgkinson, Annie, Poon, Qiuju, Li, Nathan, Orr, Anthony S, Tang, George J, Klein, Julianne, Wojciak, Joan, Campagna, Jeffrey E, Olgin, Nitish, Badhwar, Vasanth, Vedantham, Gregory M, Marcus, Pui-Yan, Kwok, Rahul C, Deo, Melvin M, Scheinman
Publikováno v:
JACC. Clinical electrophysiology. 3(3)
This study sought to investigate for an underlying genetic etiology in cases of apparent idiopathic bundle branch re-entrant ventricular tachycardia (BBRVT).BBRVT is a life-threatening arrhythmia occurring secondary to macro-re-entry within the His-P
Autor:
Julianne Wojciak, Nancy Mutsaers Thomsen, Marwan M. Refaat, Melvin M. Scheinman, Nicole Schmitt, Joan Campagna, Kirstine Calloe, Søren Grubb, Robert L. Nussbaum
Publikováno v:
Callø, K, Refaat, M M, Grubb, S, Wojciak, J, Campagna, J, Thomsen, N M, Nussbaum, R L, Scheinman, M M & Schmitt, N 2013, ' Characterization and mechanisms of action of novel Na V 1.5 channel mutations associated with Brugada syndrome ', Circulation. Arrhythmia and Electrophysiology (Online), vol. 6, no. 1, pp. 177-184 . https://doi.org/10.1161/CIRCEP.112.974220
Background— Brugada syndrome is a heterogeneous heart rhythm disorder characterized by an atypical right bundle block pattern with ST-segment elevation and T-wave inversion in the right precordial leads. Loss-of-function mutations in SCN5A encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d61ad15bb024f8d80ef6b164e12d1f0
https://curis.ku.dk/ws/files/50462895/Calloe_Circ_AE_13.pdf
https://curis.ku.dk/ws/files/50462895/Calloe_Circ_AE_13.pdf