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Circulation. Cardiovascular Genetics
|
April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermis
Torsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation
|
February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy
Torsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
European Journal of Heart Failure
|
June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope
Rasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
Scandinavian Cardiovascular Journal : SCJ
|
October 14, 2008
Moderate mitral regurgitation in patients undergoing CABG--the MoMIC trial
Per Wierup, Henrik Egeblad, Sten Lyager Nielsen, et al.
European Journal of Medical Genetics
|
March 1, 2015
A novel single nucleotide splice site mutation in FHL1 confirms an Emery-Dreifuss plus phenotype with pulmonary artery hypoplasia and facial dysmorphology
Anja E Pen, Mette Nyegaard, Mingyan Fang, et al.
Acta Anaesthesiologica Scandinavica
|
March 17, 2021
A systematic approach to weaning from extracorporeal membrane oxygenation in patients with refractory cardiac failure
Sivagowry R Mørk, Christian A Frederiksen, Roni R Nielsen, et al.
Journal of Clinical Medicine
|
November 6, 2019
Short-Term Therapies for Treatment of Acute and Advanced Heart Failure-Why so Few Drugs Available in Clinical Use, Why Even Fewer in the Pipeline?
Piero Pollesello, Tuvia Ben Gal, Dominique Bettex, et al.
International Journal of Cardiology
|
June 3, 2017
Repetitive use of levosimendan in advanced heart failure: need for stronger evidence in a field in dire need of a useful therapy
Gerhard Pölzl, Johann Altenberger, Loant Baholli, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Circulation. Cardiovascular Genetics
|
April 8, 2014
Truncating plakophilin-2 mutations in arrhythmogenic cardiomyopathy are associated with protein haploinsufficiency in both myocardium and epidermis
Torsten B Rasmussen, Peter H Nissen, Johan Palmfeldt, et al.
Human Mutation
|
February 6, 2013
Mutated desmoglein-2 proteins are incorporated into desmosomes and exhibit dominant-negative effects in arrhythmogenic right ventricular cardiomyopathy
Torsten B Rasmussen, Johan Palmfeldt, Peter H Nissen, et al.
European Journal of Heart Failure
|
June 27, 2018
The clinical outcome of LMNA missense mutations can be associated with the amount of mutated protein in the nuclear envelope
Rasha A Al-Saaidi, Torsten B Rasmussen, Rune I D Birkler, et al.
Scandinavian Cardiovascular Journal : SCJ
|
October 14, 2008
Moderate mitral regurgitation in patients undergoing CABG--the MoMIC trial
Per Wierup, Henrik Egeblad, Sten Lyager Nielsen, et al.
European Journal of Medical Genetics
|
March 1, 2015
A novel single nucleotide splice site mutation in FHL1 confirms an Emery-Dreifuss plus phenotype with pulmonary artery hypoplasia and facial dysmorphology
Anja E Pen, Mette Nyegaard, Mingyan Fang, et al.
Acta Anaesthesiologica Scandinavica
|
March 17, 2021
A systematic approach to weaning from extracorporeal membrane oxygenation in patients with refractory cardiac failure
Sivagowry R Mørk, Christian A Frederiksen, Roni R Nielsen, et al.
Journal of Clinical Medicine
|
November 6, 2019
Short-Term Therapies for Treatment of Acute and Advanced Heart Failure-Why so Few Drugs Available in Clinical Use, Why Even Fewer in the Pipeline?
Piero Pollesello, Tuvia Ben Gal, Dominique Bettex, et al.
International Journal of Cardiology
|
June 3, 2017
Repetitive use of levosimendan in advanced heart failure: need for stronger evidence in a field in dire need of a useful therapy
Gerhard Pölzl, Johann Altenberger, Loant Baholli, et al.
Page
of 5