905 results on '"Chevalier, Philippe"'
Search Results
2. Distinct Substrates of Idiopathic Ventricular Fibrillation Revealed by Arrhythmia Characteristics on Implantable Cardioverter-Defibrillator
3. Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
4. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS Substudy
5. Wearable electrocardiogram devices in patients with congenital long QT syndrome: The SMART-QT study
6. Deep Reinforcement Learning for inventory optimization with non-stationary uncertain demand
7. Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome
8. Personalized screening before subcutaneous cardioverter-defibrillator implantation: Usefulness and outcomes in clinical practice—the S-ICD screening SIS prospective study
9. Managing priorities on on-demand service platforms with waiting time differentiation
10. ISE/ISHNE Expert Consensus Statement on ECG Diagnosis of Left Ventricular Hypertrophy: The Change of the Paradigm. The joint paper of the International Society of Electrocardiology and the International Society for Holter Monitoring and Noninvasive Electrocardiology
11. Self-administered intranasal etripamil using a symptom-prompted, repeat-dose regimen for atrioventricular-nodal-dependent supraventricular tachycardia (RAPID): a multicentre, randomised trial
12. Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants
13. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation
14. Method for encoding and decoding variables in engineering problems
15. Purchasing together or alone? Tradeoffs for information sharing
16. Post-Translational Modifications and Diastolic Calcium Leak Associated to the Novel RyR2-D3638A Mutation Lead to CPVT in Patient-Specific hiPSC-Derived Cardiomyocytes.
17. CMR - Late gadolinium enhancement characteristics associated with monomorphic ventricular arrhythmia in patients with non-ischemic cardiomyopathy
18. Genetic associations of protein-coding variants in human disease
19. Incidence, Risk Factors, and Outcomes of Atrial Arrhythmias in Adult Patients With Atrioventricular Septal Defect
20. NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis
21. Impact of Pulmonary Valve Replacement on Ventricular Arrhythmias in Patients With Tetralogy of Fallot and Implantable Cardioverter-Defibrillator
22. New design of a magnetic device for wide-angle XYZ polarization analysis PASTIS-3, from the concept to first tests with thermal neutrons
23. Abstract 14023: Myocardial Perfusion Abnormalities: A Potential Biomarker for Ventricular Arrhythmias in Hypertrophic Cardiomyopathy Young Patients?
24. Epigenetics in atrial fibrillation: A reappraisal
25. A Primary Prevention Clinical Risk Score Model for Patients With Brugada Syndrome (BRUGADA-RISK)
26. Green tea and nadolol interaction: A risk of therapeutic inefficiency, a case report and extensive review
27. Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center’s Experience Over 5 Years
28. Atrial premature activity detected after an ischaemic stroke unveils atrial myopathy
29. High Frame Rate Ultrasound for Electromechanical Wave Imaging to Differentiate Endocardial From Epicardial Myocardial Activation
30. ISE/ISHNE expert consensus statement on the ECG diagnosis of left ventricular hypertrophy: The change of the paradigm
31. Green tea and nadolol interaction: A risk of therapeutic inefficiency, a case report and extensive review
32. Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methods
33. TRPM4 mutations to cause autosomal recessive and not autosomal dominant Brugada type 1 syndrome
34. Vascular protease‐activated receptor 4 upregulation, increased platelet aggregation, and coronary lipid deposits induced by long‐term dabigatran administration – results from a diabetes animal model
35. A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation
36. Exclusion of Intra-Atrial Thrombus Diagnosis Using D-Dimer Assay Before Catheter Ablation of Atrial Fibrillation
37. Myocardial Thermal Ablation with a Transesophageal High-Intensity Focused Ultrasound Probe: Experiments on Beating Heart Models
38. ISE/ISHNE expert consensus statement on the ECG diagnosis of left ventricular hypertrophy: The change of the paradigm.
39. From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies
40. Self-administered intranasal etripamil using a symptom-prompted, repeat-dose regimen for atrioventricular-nodal-dependent supraventricular tachycardia (RAPID): a multicentre, randomised trial
41. Joint dynamic pricing and lot-sizing under competition
42. Assessment of potential heart donors: A statement from the French heart transplant community
43. Atrial fibrillation: Neurogenic or myogenic?
44. Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant
45. Prolonged Piezo1 Activation Induces Cardiac Arrhythmia
46. Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies
47. Atrial fibrillation is associated with hypermethylation in human left atrium, and treatment with decitabine reduces atrial tachyarrhythmias in spontaneously hypertensive rats
48. A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband
49. Spironolactone as a Potential New Treatment to Prevent Arrhythmias in Arrhythmogenic Cardiomyopathy Cell Model
50. OPTIMIZING THE DESIGN OF AN ASSEMBLY LINE
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