نتایج جستجو برای: calcium channelopathy
تعداد نتایج: 167790 فیلتر نتایج به سال:
convulsion is one of the most common problems in children and hypocalcemia is one the most frequent etiological items in children’s convulsion. corrected qt (qtc) in ekg is prolonged in hypocalcemia, so it can be a useful tool for evaluation of serum ionized calcium. in three groups (first seizure, multiple seizures, without seizure or control ) every 25 cases, qtc, serum ionized ca, total ca, ...
Traumatic brain injury is a major cause of death and disability worldwide and often associated with post-traumatic epilepsy. We recently demonstrated that TBI induces acquired GABAA receptors channelopathy that associates with hyperexcitability in granule cell layer (GCL). We now assessed the expression of GABAA and GABAB receptor subunit mRNAs between 6 h and 6 months post-TBI in the hippocamp...
BACKGROUND Congenital long-QT syndrome (LQTS) is a primary arrhythmogenic syndrome stemming from perturbed cardiac repolarization. LQTS, which affects approximately 1 in 3000 persons, is 1 of the most common causes of autopsy-negative sudden death in the young. Since the sentinel discovery of cardiac channel gene mutations in LQTS in 1995, hundreds of mutations in 8 LQTS susceptibility genes ha...
CONTEXT The congenital long QT syndrome (LQTS) is an inherited channelopathy known for its electrocardiographic manifestations of QT prolongation and its hallmark arrhythmia, torsades de pointes (TdP). TdP can lead to syncope or sudden death and is often precipitated by triggers such as physical exertion or emotional stress. Given that athletes may be at particular risk for adverse outcomes, th...
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