1,030 results on '"Chevalier, Philippe"'
Search Results
2. G\'en\'eration de bases de donn\'ees images IR sous contraintes avec variabilit\'e thermique intrins\`eque des cibles
3. METRIC: a complete methodology for performances evaluation of automatic target Detection, Recognition and Tracking algorithms in infrared imagery
4. Viral myocarditis in combination with genetic cardiomyopathy as a cause of sudden death. An autopsy series
5. Distinct Substrates of Idiopathic Ventricular Fibrillation Revealed by Arrhythmia Characteristics on Implantable Cardioverter-Defibrillator
6. Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases
7. Personalized screening before subcutaneous cardioverter-defibrillator implantation: Usefulness and outcomes in clinical practice—the S-ICD screening SIS prospective study
8. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS Substudy
9. Wearable electrocardiogram devices in patients with congenital long QT syndrome: The SMART-QT study
10. Deep Reinforcement Learning for inventory optimization with non-stationary uncertain demand
11. 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
12. Managing priorities on on-demand service platforms with waiting time differentiation
13. 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
14. Self-administered intranasal etripamil using a symptom-prompted, repeat-dose regimen for atrioventricular-nodal-dependent supraventricular tachycardia (RAPID): a multicentre, randomised trial
15. 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
16. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation
17. Method for encoding and decoding variables in engineering problems
18. Purchasing together or alone? Tradeoffs for information sharing
19. CMR - Late gadolinium enhancement characteristics associated with monomorphic ventricular arrhythmia in patients with non-ischemic cardiomyopathy
20. Genetic associations of protein-coding variants in human disease
21. Incidence, Risk Factors, and Outcomes of Atrial Arrhythmias in Adult Patients With Atrioventricular Septal Defect
22. Post-Translational Modifications and Diastolic Calcium Leak Associated to the Novel RyR2-D3638A Mutation Lead to CPVT in Patient-Specific hiPSC-Derived Cardiomyocytes.
23. Impact of Pulmonary Valve Replacement on Ventricular Arrhythmias in Patients With Tetralogy of Fallot and Implantable Cardioverter-Defibrillator
24. New design of a magnetic device for wide-angle XYZ polarization analysis PASTIS-3, from the concept to first tests with thermal neutrons
25. Epigenetics in atrial fibrillation: A reappraisal
26. A Primary Prevention Clinical Risk Score Model for Patients With Brugada Syndrome (BRUGADA-RISK)
27. Abstract 14023: Myocardial Perfusion Abnormalities: A Potential Biomarker for Ventricular Arrhythmias in Hypertrophic Cardiomyopathy Young Patients?
28. Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center’s Experience Over 5 Years
29. Atrial premature activity detected after an ischaemic stroke unveils atrial myopathy
30. High Frame Rate Ultrasound for Electromechanical Wave Imaging to Differentiate Endocardial From Epicardial Myocardial Activation
31. NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis
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. Green tea and nadolol interaction: A risk of therapeutic inefficiency, a case report and extensive review
38. Myocardial Thermal Ablation with a Transesophageal High-Intensity Focused Ultrasound Probe: Experiments on Beating Heart Models
39. ISE/ISHNE expert consensus statement on the ECG diagnosis of left ventricular hypertrophy: The change of the paradigm
40. Green tea and nadolol interaction: A risk of therapeutic inefficiency, a case report and extensive review
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. From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies
45. Self-administered intranasal etripamil using a symptom-prompted, repeat-dose regimen for atrioventricular-nodal-dependent supraventricular tachycardia (RAPID): a multicentre, randomised trial
46. Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant
47. Atrial fibrillation is associated with hypermethylation in human left atrium, and treatment with decitabine reduces atrial tachyarrhythmias in spontaneously hypertensive rats
48. ISE/ISHNE expert consensus statement on the ECG diagnosis of left ventricular hypertrophy: The change of the paradigm.
49. SEMA3A as a biomarker of primary ventricular fibrillation complicating STEMI
50. A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband
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