Mots-clés
 > MYOBASE > SANTE > médecine > spécialité médicale > cardiologie-angiologie > maladie cardiovasculaire > maladie cardiaque > cardiomyopathie
cardiomyopathieSynonyme(s)cardiac myopathy ;heart myopathy ;maladie du myocarde ;myocardial disease ;myocardiopathie ;myocardiopathy ;myopathie cardiaque cardiomyopathy |
Documents disponibles dans cette catégorie (1081)
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Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro
Perepelina K, Klauzen P, Khudiakov A, et al.
Stem cell research, 2020, 43
Synemin-related skeletal and cardiac myopathies: an overview of pathogenic variants
Paulin D, Hovhannisyan Y, Kasakyan S, et al.
American journal of physiology. Cell physiology, 2020
Myasthenic crises triggering Takotsubo cardiomyopathy
Scorza FA, Fiorini AC, Scorza CA, et al.
International journal of cardiology, 2020, 300, p 48
Reply to: Myasthenic crises triggering Takotsubo cardiomyopathy
Desai R, Sachdeva R, Kumar G
International journal of cardiology, 2020, 300, p 47
ERK1/2 Phosphorylation of FHOD Connects Signaling and Nuclear Positioning Alternations in Cardiac Laminopathy
Antoku S, Wu W, Joseph LC, et al.
Developmental cell, 2019, 51, 5, p 602
Lamin A/C Cardiomyopathy: Implications for Treatment
Chen SN, Sbaizero O, Taylor MRG, et al.
Current Cardiology Reports, 2019, 21, 12, p 160
Risk Stratification for Sudden Cardiac Death in Non-Ischaemic Dilated Cardiomyopathy
Akhtar M, Elliott PM
Current Cardiology Reports, 2019, 21, 12, p 155
Myopathie de Duchenne : la spironolactone, un protecteur cardiaque à court terme
Schanen-Bergot MO
2019
Dystrophie musculaire de Duchenne et de Becker : les freins au suivi cardiologique aux Etats-Unis chez les femmes symptomatiques
Urtizberea JA
2019
Emery-Dreifuss muscular dystrophy: focal point nuclear envelope
Muchir A, Worman HJ
Current opinion in neurology, 2019, 32, 5, p 728
Burden and impact of takotsubo syndrome in myasthenic crisis: A national inpatient perspective on the under-recognized but potentially fatal association
Desai R, Abbas SA, Fong HK, et al.
International journal of cardiology, 2019
Gene Therapy Rescues Cardiac Dysfunction in Duchenne Muscular Dystrophy Mice by Elevating Cardiomyocyte Deoxy-Adenosine Triphosphate
Kolwicz SC Jr, Hall JK, Moussavi-Harami F, et al.
JACC. Basic to translational science, 2019, 4, 7, p 778
Stabilization of Early Duchenne Cardiomyopathy With Aldosterone Inhibition: Results of the Multicenter AIDMD Trial
Raman SV, Hor KN, Mazur W, et al.
Journal of the American Heart Association, 2019, 8, 19
Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy
Gigli M, Merlo M, Graw SL, et al.
Journal of the American College of Cardiology, 2019, 74, 11, p 1480
Maladies mitochondriales à expression musculaire : un nouveau gène en cause (COX6A2)
Urtizberea JA
2019
Cardiac Pathophysiology and the Future of Cardiac Therapies in Duchenne Muscular Dystrophy
Meyers TA, Townsend D
International Journal of molecular sciences, 2019, 20, 17
Young Becker Muscular Dystrophy Patients Demonstrate Fibrosis Associated With Abnormal Left Ventricular Ejection Fraction on Cardiac Magnetic Resonance Imaging
Johnston TP, Cripe LH, Mah ML, et al.
Circulation. Cardiovascular imaging, 2019, 12, 7
Salih Myopathy : Synonym: Early-Onset Myopathy with Fatal Cardiomyopathy
Hackman P, Savarese M, Carmignac V, et al.
GeneReviews® [Internet], 2019
Defining Features of Patients who Develop Takotsubo Cardiomyopathy during Myasthenic Crisis: A Systematic Review of Case Studies
Kariyanna PT, Sutarjono B, Jayarangaiah A, et al.
American journal of medical case reports, 2019, 7, 9, p 203
La ventilation assistée aurait un bénéfice indirect sur la fonction myocardique dans les certaines sarcoglycanopathies
Urtizberea JA
2018
Andersen-Tawil Syndrome : Synonym: Long QT Syndrome Type 7 (LQTS Type 7)
Veerapandiyan A, Statland JM, Tawil R
GeneReviews® [Internet], 2018
