385 results on '"Medeiros-Domingo, Argelia"'
Search Results
52. Role of genetic testing in young patients with idiopathic atrioventricular conduction disease.
53. Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts
54. Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy
55. An International Evidence Based Reappraisal of Genes Associated with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) using the ClinGen Framework
56. Filamin C missense variant associated with severe right atrial disease and skeletal myopathy
57. Familial dilated cardiomyopathy associated with a novel heterozygous RYR2 early truncating variant
58. International Evidence Based Reappraisal of Genes Associated with Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework
59. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
60. Clinical and Genetic Characteristics of Long QT Syndrome
61. Clínica y genética en el síndrome de QT largo
62. Clinical impact of low coverage in whole-exome genetic testing in the assessment of familial arrhythmogenic right ventricular cardiomyopathy: a case report
63. Right Ventricle Best Predicts the Race Performance in Amateur Ironman Athletes
64. Familial dilated cardiomyopathy associated with a novel heterozygous RYR2 early truncating variant
65. Sex-Related Differences in Cardiac Channelopathies
66. Impact of Genetic Variant Reassessment on the Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy Based on the 2010 Task Force Criteria
67. Familial Arrhythmogenic Cardiomyopathy: Clinical Determinants of Phenotype Discordance and the Impact of Endurance Sports
68. Potenciales efectos pro-arrítmicos de la farmacoterapia contra SARS-CoV-2
69. Loss-of-function mutation of the SCN3B-encoded sodium channel β3 subunit associated with a case of idiopathic ventricular fibrillation
70. Association of Congenital, Diffuse Electrical Disease in Children with Normal Heart: Sick Sinus Syndrome, Intraventricular Conduction Block, and Monomorphic Ventricular Tachycardia
71. Out-of-hospital cardiac arrest due to idiopathic ventricular fibrillation in patients with normal electrocardiograms:results from a multicentre long-term registry
72. Erratum to: Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases
73. A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia
74. Familial Arrhythmogenic Cardiomyopathy: Clinical Determinants of Phenotype Discordance and the Impact of Endurance Sports
75. How to Reach the Left Atrium in Atrial Fibrillation Ablation?
76. Potenciales efectos proarrítmicos de la farmacoterapia contra SARS-CoV-2
77. Outcome of video-assisted thoracoscopic implantation of epicardial left ventricular leads with visual targeting for cardiac resynchronization therapy
78. Out-of-hospital cardiac arrest due to idiopathic ventricular fibrillation in patients with normal electrocardiograms: results from a multicentre long-term registry
79. Molecular and genetic insights into progressive cardiac conduction disease
80. Phenotypic Spectrum of Mutations: A Clinical Case
81. Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice
82. Idiopathic Ventricular Fibrillation and Otherwise Normal Electrocardiograms
83. Comparison of lead failure manifestation of Biotronik Linox with St. Jude Medical Riata and Medtronic Sprint Fidelis lead
84. An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis
85. Unexplained Cardiac Arrest in an Apparently Healthy Young Woman
86. Late-onset severe long QT syndrome.
87. Unexplained cardiac arrest:a tale of conflicting interpretations of KCNQ1 genetic test results
88. Phenotypic Spectrum of HCN4 Mutations:A Clinical Case
89. Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability
90. Post-mortem whole-exome sequencing(WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death(SUD) cases
91. Failure Rate and Conductor Externalization of the Biotronik Linox / Sorin Vigila Implantable Cardioverter Defibrillator Lead
92. Late-onset severe long QT syndrome
93. Arrhythmogenic right ventricular cardiomyopathy vs. dilated cardiomyopathy: implications for next-generation sequencing and microRNA regulation in appropriate diagnosis—Authors' reply
94. Outcome of video-assisted thoracoscopic implantation of epicardial left ventricular leads with visual targeting for cardiac resynchronization therapy.
95. Sports-related sudden cardiac deaths in the young population of Switzerland
96. Das interessante EKG. EKG bei einem Kleinkind: gefährlich?
97. Sports-related sudden cardiac deaths in the young population of Switzerland
98. Sex hormones affect outcome in arrhythmogenic right ventricular cardiomyopathy/dysplasia: from a stem cell derived cardiomyocyte-based model to clinical biomarkers of disease outcome
99. Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases
100. 176-48: Lead failure rate and failure manifestation of the Biotronik Linox lead compared to the St. Jude Medical Riata lead and the Medtronic Sprint Fidelis lead
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