[PDF] Top 20 Investigación de la comunicación, incertidumbre y conocimiento de la sociedad
Has 10000 "Investigación de la comunicación, incertidumbre y conocimiento de la sociedad" found on our website. Below are the top 20 most common "Investigación de la comunicación, incertidumbre y conocimiento de la sociedad".
Electrocardiographic T-wave parameters in families with long QT syndrome
... The data was exported from an Excel v. 2010 data- sheet to the STATISTICA v. 7.1 data analysis software system (StatSoft Inc. 2006, Kraków, Poland). Due to the lack of normal distribution of the investigated pa- ... See full document
146
Locus heterogeneity of autosomal dominant long QT syndrome
... dominant long QT syndrome (LQT) is an inherited disorder that causes syncope and sudden death from cardiac ...unrelated families we mapped a gene for LQT to the short arm of chromosome 11 ... See full document
108
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes
... LQTS families [11, ...loss families along the same pathways. Such families existed in the new habitat because a parish meeting protocol (of 1831) informed that “deaf mute children at age 11 to 14 ... See full document
31
Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias
... with long QT syndrome (LQTS) ...prolonged QT intervals (Figure ...and QT prolonga- ...deafness, QT prolon- gation, and recurrent syncope in five children from two independent ... See full document
26
Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families
... Background: Long QT syndrome (LQTS) is characterized by the prolongation of QT interval, which results in syncope and sudden cardiac death in young ...Iranian families with a history of ... See full document
10
Congenital long QT syndrome
... goes through life without ever suffering cardiac events. Despite a more serious clinical pattern, it has to be noted that also among LQT2 and LQT3 patients almost half remains asymptomatic; this fact is often forgotten ... See full document
9
MOLECULAR ASPECTS OF LONG QT SYNDROME
... Congenital long QT syndrome (LQTs) is a hereditary, heterogeneous group of cardiac diseases characterised by a prolongation of the QT ...and electrocardiographic abnormalities ... See full document
157
Diagnosis of long QT syndrome via support vector machines classification
... Congenital Long QT Syndrome (LQTS) is a genetic disease and associated with significant arrhythmias and sudden cardiac ...with parameters = ... See full document
90
KvLQT1 and KCNE1 K+ Channel Gene Polymorphisms in Long QT Syndrome
... exhibited Long QT syndrome when compared to ...the Long QT syndrome patients was found to be ...acquired Long QT Syndrome (aLQTS), exhibited hypokalemia with ... See full document
11
Determination the Normal Parameters (amplitude and duration) of Electrocardiogram Waves in River Buffaloes (Bubalus Bubalis) of Khuzestan
... Rezakhani and Holmes have shown that age is one of the affecting factors on ventricular depolarization vector in human and cattle (Holmes and Rezakhani, 1975). Upadhyay et al. (1976), in a study on Jersey cattle, showed ... See full document
5
A Rare Case of the Digenic Inheritance of Long QT Syndrome Type 2 and Type 6
... arrhythmias and symptoms such as syncope and cardiac arrest [9, 10]. Furthermore, the onset of cardiac events in digenic inheritance is at a significantly younger age (10 ± 8 years vs 18 ± 16 years) [11]. However, our ... See full document
143
A revised view of cardiac sodium channel “blockade” in the long QT syndrome
... Here we report that the R1623Q Na channel is unusu- ally sensitive to lidocaine. Surprisingly, we find that lido- caine neither plugs the open channel, nor repairs the inactivation of open channels as proposed previously ... See full document
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Improving Long QT Syndrome diagnosis using machine learning on ECG characteristics
... A publicly available package, ‘glmnet’, was used for model training and testing. [23] Subjects were classified as LQTS or healthy by a machine learning trained classification model, based on multiple inputs, see section ... See full document
148
Cardiac Manifestations of Congenital Generalized Lipodystrophy
... from long QT syndrome and a predisposition to tachyarrhythmias, including cate- cholaminergic polymorphic ventric- ular tachycardia and sudden cardiac ... See full document
13
Insights into the molecular mechanisms of bradycardia triggered arrhythmias in long QT 3 syndrome
... Congenital long QT syndrome is a rare disease in which the electrocardiogram QT interval is prolonged due to dysfunctional ventricular ... See full document
59
Identification of a Family With Inherited Long QT Syndrome After a Pediatric Near-drowning
... “black-outs,” fainting, syncope, seizures not respon- sive to usual antiepileptic therapy, or any unex- plained accidents occurring previously in the drown- ing victim or any related family members. Further, a 12-lead ... See full document
25
Successful Parental Use of an Automated External Defibrillator for an Infant With Long-QT Syndrome
... Congenital long-QT syndrome with 2:1 atrioventricular block presenting in the perinatal period is rare, has a poor prognosis, and leads to high risk for lethal ventricular arrhythmic ...with ... See full document
6
Mechanisms of cardiac arrhythmias and sudden death in transgenic rabbits with long QT syndrome
... Student’s t test (paired and unpaired) was used to com- pare the means of 2 groups, and Mann-Whitney and Wilcoxon matched- pairs test was used for values not normally ... See full document
125
Drug mediated shortening of action potentials in LQTS2 hiPSC cardiomyocytes
... HERG is a more feasible route. Most drug interaction with this channel induces prolongation of QT interval and is a major risk factor that is considered in pharmaceutical drug development [47]. Indeed, as part of ... See full document
47
Genetics of acquired long QT syndrome
... Examples of acquired long QT syndrome. A common fea- ture is a pause (often after an ectopic beat), indicated by a star, with deranged repolarization in the following cycle (red arrows). (A) ... See full document
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