نتایج جستجو برای: potassium channelopathy

تعداد نتایج: 77926  

Journal: :The Journal of pharmacology and experimental therapeutics 2004
Lin Wu John C Shryock Yejia Song Yuan Li Charles Antzelevitch Luiz Belardinelli

Prolongation of the QT interval of the ECG is associated with increased risk of torsades de pointes ventricular tachycardia. Ranolazine, a novel antianginal agent, is reported to decrease the delayed rectifier potassium current, I(Kr), and to increase action potential duration (APD) and the QT interval. However, ranolazine is also reported to reduce late sodium current (late I(Na)), a depolariz...

Journal: :Journal of Clinical and Translational Science 2020

2015
Muthiah Subramanian N. Senthil S. Sujatha

Inherited channelopathies are a heterogeneous group of disorders resulting from dysfunction of ion channels in cellular membranes. They may manifest as diseases affecting skeletal muscle contraction, the conduction system of the heart, nervous system function, and vision syndromes. We describe a family of South Indian descent with hypokalemic periodic paralysis in which four members also have i...

Journal: :Internal medicine 2003
Akira Tamaoka

Paramyotonia congenita, the major characteristics of which are cold-induced and exercise-induced myotonia, is an autosomal-dominant muscle disease which is classified into one of a group of muscle diseases, so-called muscle "sodium channelopathies" caused by missense mutations in the gene coding for the skeletal muscle sodium channel a-subunit (SCN4A) (1-4). Such muscle sodium channelopathies s...

2016
Rahima Begum Yamina Bakiri Kirill E. Volynski Dimitri M. Kullmann

Brain development and interictal function are unaffected in many paroxysmal neurological channelopathies, possibly explained by homoeostatic plasticity of synaptic transmission. Episodic ataxia type 1 is caused by missense mutations of the potassium channel Kv1.1, which is abundantly expressed in the terminals of cerebellar basket cells. Presynaptic action potentials of small inhibitory termina...

Journal: :Science Translational Medicine 2019

Journal: :genetics in the 3rd millennium 0
امید آریانی omid ariyani مسعود هوشمند masoud houshmand سین دادگر s dadgar میم جمالی m jamali میم روحی مقدم m roohimoghadam

characterized by muscle stiffness and an inability of the muscle to quickly relax after voluntary contraction. although myotonia can affect any skeletal muscles, including muscles of the face and tongue, it occurs most often in the legs. myotonia causes muscle stiffness (a myotonic disorder should be considered in the differential diagnosis of a patient complaining of muscle stiffness) that can...

2013
Stelios Paraskevaidis Efstratios K Theofilogiannakos Vasileios Kamperidis Yiannis S Chatzizisis Konstantinos Tsilonis Vassilios P Vassilikos George Dakos George Stavropoulos Antonios Ziakas Stavros Hadjimiltiades Ioannis H Styliadis

Brugada syndrome is an inherited channelopathy associated with an increased risk of syncope and sudden cardiac death. In rare cases it can be manifested with electrical storm. We report two cases of Brugada syndrome that presented with electrical storm and were treated successfully with oral quinidine, an "endangered species" drug.

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