نتایج جستجو برای: potassium channelopathy

تعداد نتایج: 77926  

Journal: :Journal of the American College of Cardiology 2021

Journal: :Brain : a journal of neurology 2012
Susan E Tomlinson Hugh Bostock Bronwyn Grinton Michael G Hanna Dimitri M Kullmann Matthew C Kiernan Ingrid E Scheffer Samuel F Berkovic David Burke

Benign familial neonatal epilepsy is a neuronal channelopathy most commonly caused by mutations in KCNQ2, which encodes the K(v)7.2 subunit of the slow K(+) channel. K(v)7.2 is expressed in both central and peripheral nervous systems. Seizures occur in the neonatal period, often in clusters within the first few days of life, and usually remit by 12 months of age. The mechanism of involvement of...

2013
Veronica Sansoni Matilde Forcella Alessandra Mozzi Paola Fusi Roberto Ambrosini Luigi Ferini-Strambi Romina Combi

Nocturnal frontal lobe epilepsy has been historically considered a channelopathy caused by mutations in subunits of the neuronal nicotinic acetylcholine receptor or in a recently reported potassium channel. However, these mutations account for only a minority of patients, and the existence of at least a new locus for the disease has been demonstrated. In 2005, we detected two nucleotide variati...

2006
Andrew H Smith Frank A Fish Prince J Kannankeril

Andersen-Tawil syndrome (ATS) is a rare condition consisting of ventricular arrhythmias, periodic paralysis, and dysmorphic features. In 2001, mutations in KCNJ2, which encodes the a subunit of the potassium channel Kir2.1, were identified in patients with ATS. To date, KCNJ2 is the only gene implicated in ATS, accounting for approximately 60% of cases. ATS is a unique channelopathy, and repres...

Journal: :Journal of the American Society of Nephrology : JASN 2010
David M Williams Coeli M B Lopes Avia Rosenhouse-Dantsker Heather L Connelly Alessandra Matavel Jin O-Uchi Elena McBeath Daniel A Gray

SeSAME/EAST syndrome is a channelopathy consisting of a hypokalemic, hypomagnesemic, metabolic alkalosis associated with seizures, sensorineural deafness, ataxia, and developmental abnormalities. This disease links to autosomal recessive mutations in KCNJ10, which encodes the Kir4.1 potassium channel, but the functional consequences of these mutations are not well understood. In Xenopus oocytes...

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2007

Journal: :Journal of Biological Chemistry 2010

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