[PDF] Top 20 The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance
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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance
... modulating the risk of Brugada ECG phenotype. To explore the potential role of common genetic variants in susceptibility to Brs, we have recently coordinated an international genome- wide association ... Voir le document complet
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Brugada syndrome: Diagnosis, risk stratification and management
... Summary Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of sudden cardiac death, despite a structurally normal ...on a specific ... Voir le document complet
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Dynamic changes in ventricular depolarization during exercise in patients with Brugada syndrome
... patients with BS, related to the QRS complex. For instance, a longer QRS duration in symptomatic patients have been observed in lead V2 ...associated with increased risk of cardiac ... Voir le document complet
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Common and rare variant analysis in early-onset bipolar disorder vulnerability.
... Bipolar disorder is one of the most common and devastating psychiatric disorders whose mechanisms remain largely ...Despite a strong genetic contribution demonstrated by twin and adoption studies, ... Voir le document complet
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View of Preterm Birth: An Inflammatory Syndrome, Not Just A Myometrial Disorder
... néonatale a considérablement diminuée avec les récentes avancées en néonatalogie, l’incidence de la naissance préma- turée et de ses complications sont en ... Voir le document complet
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EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alstrom syndrome and Bardet-Biedl syndrome.
... Bardet-Biedl syndrome Bardet-Biedl syndrome (BBS) (OMIM 209900) is charac- terized by early onset retinal dystrophy, obesity, and frequent polydactyly ...associated with BBS ... Voir le document complet
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Caractéristiques et facteurs prédictifs d’une réponse majeure lors de test à l’ajmaline ou flécaine chez les patients avec syndrome de Brugada
... du syndrome de Brugada (40) , le substrat pathologique a été observé uniquement dans la chambre de chasse ventriculaire droite en comparaison aux sujets ... Voir le document complet
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The coeruleus/subcoeruleus complex in idiopathic rapid eye movement sleep behaviour disorder
... 1991). The Grooved Pegboard Test was used to evaluate motor dexterity and visual-manual coordination and involved a task of inserting 25 sticks into 25 holes as rapidly as possible (Lafayette Instruments, ... Voir le document complet
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PAC: Privacy-Preserving Arrhythmia Classification with Neural Networks
... perform arrhythmia predictions in batches, namely, with several heartbeat ...as the classification of a single heartbeat may not be sufficient to diagnose the disease for a ... Voir le document complet
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Heart rate differences between symptomatic and asymptomatic Brugada syndrome patients at night
... during the last period of sleep. The results suggest that symptomatic patients may be related to lower heart rate variability and complexity values, as well as to greater circadian fluctuations ... Voir le document complet
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Stratification du risque de mort subite chez les patients présentant un syndrome de Brugada et un aspect de repolarisation précoce
... INTRODUCTION Brugada Syndrome (BrS) is an inherited arrhythmia syndrome first described in 1992 by Pedro and Josep Brugada 1 affecting ionic channels mainly located in the ... Voir le document complet
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Multivariate classification of Brugada syndrome patients based on autonomic response to exercise testing
... play a relevant role in the arrhythmogenesis of the disease [ 7 , 8 ...Moreover, a sympathetic autonomic dysfunction on BS patients has been reported in previous works on cardiac autonomic ... Voir le document complet
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Sodium-channel blocker challenge in the familial screening of Brugada syndrome: safety and predictors of positivity
... Sodium- channel blocker challenge in the familial screening of Brugada syndrome: safety and predictors of positivity.4. M AN US CR IP T AC CE PT ED 1.[r] ... Voir le document complet
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A prospective, longitudinal, study of men with borderline personality disorder with and without comorbid antisocial personality disorder
... of the 241 who con- sented to a criminal record check, ...acquired a criminal record. Diagnostic interviews revealed that 11.9% of the men met criteria for BPD, and two-thirds of them, also ... Voir le document complet
13
Supporting Parents of a Child with Autism Spectrum Disorder: The French Awakening
... of a child with ASD is probably one of the many collateral damages of a painful history marked by psychogenic theories incriminating mothers for their child’s disturbances (Greenberg et ... Voir le document complet
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Uncoupling of the endocannabinoid signalling complex in a mouse model of fragile X syndrome
... mice, a form of long-term depression (LTD) that requires mGlu 5 receptor-mediated protein synthesis 3–7 ...of the ventral striatum and pyramidal neurons of the prefrontal cortex (PFC), activation of ... Voir le document complet
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A Survey on Reverse Inheritance Class Relationship
... reverse inheritance has a great potential. It can be seen as a class relationship in the object-oriented ...as a class hierarchy reorganization tool with restricted adaptation ... Voir le document complet
5
Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndrome
... Philippe Maury, Frédéric Sacher, Jean-Baptiste Gourraud, Jean-Luc Pasquié, Franck Raczka, Vanina Bongard, Alexandre Duparc, Pierre Mondoly, Marie. Sadron, Stéphanie Chatel, et al[r] ... Voir le document complet
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Many-body-localization transition in the strong disorder limit : entanglement entropy from the statistics of rare extensive resonances
... displaying a Many-Body- Localization Transition seems sufficiently rich to produce critical points with level statistics inter- polating continuously between the Poisson statistics of the ... Voir le document complet
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Integrated clinical and omics approach to rare diseases novel genes and oligogenic inheritance in holoprosencephaly
... addressed the relevance of oligogenic model for unsolved HPE ...that the onset of HPE arises from the combined effects of hypomorphic variants in several genes belonging to critical biological ... Voir le document complet
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