Literature DB >> 12849484

Neurological disorders caused by inherited ion-channel mutations.

Dimitri M Kullmann1, Michael G Hanna.   

Abstract

Several neurological diseases-including neuromuscular disorders, movement disorders, migraine, and epilepsy-are caused by inherited mutations of ion channels. The list of these "channelopathies" is expanding rapidly, as is the phenotypic range associated with each channel. At present the best understood channelopathies are those that affect muscle-fibre excitability. These channelopathies produce a range of disorders which include: periodic paralysis, myotonias, malignant hyperthermia, and congenital myasthenic syndromes. By contrast, the mechanisms of diseases caused by mutations of ion channels that are expressed in neurons are less well understood. However, as for the muscle channelopathies, a striking feature is that many neuronal channelopathies cause paroxysmal symptoms. This review summarises the clinical features of the known neurological channelopathies, within the context of the functions of the individual ion channels.

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Year:  2002        PMID: 12849484     DOI: 10.1016/s1474-4422(02)00071-6

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN: 1474-4422            Impact factor:   44.182


  16 in total

Review 1.  Muscle channelopathies and critical points in functional and genetic studies.

Authors:  Karin Jurkat-Rott; Frank Lehmann-Horn
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

Review 2.  Mutational consequences of aberrant ion channels in neurological disorders.

Authors:  Dhiraj Kumar; Rashmi K Ambasta; Pravir Kumar
Journal:  J Membr Biol       Date:  2014-08-14       Impact factor: 1.843

3.  Novel CACNA1A mutation(s) associated with slow saccade velocities.

Authors:  Stefan Kipfer; Simon Jung; Johannes R Lemke; Anna Kipfer-Kauer; Jeremy P Howell; Alain Kaelin-Lang; Thomas Nyffeler; Klemens Gutbrod; Angela Abicht; René M Müri
Journal:  J Neurol       Date:  2013-09-18       Impact factor: 4.849

Review 4.  Episodic ataxia type 2.

Authors:  Michael Strupp; Andreas Zwergal; Thomas Brandt
Journal:  Neurotherapeutics       Date:  2007-04       Impact factor: 7.620

5.  K+-dependent paradoxical membrane depolarization and Na+ overload, major and reversible contributors to weakness by ion channel leaks.

Authors:  Karin Jurkat-Rott; Marc-André Weber; Michael Fauler; Xiu-Hai Guo; Boris D Holzherr; Agathe Paczulla; Nikolai Nordsborg; Wolfgang Joechle; Frank Lehmann-Horn
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-18       Impact factor: 11.205

6.  Achieving synaptically relevant pulses of neurotransmitter using PDMS microfluidics.

Authors:  E J Botzolakis; A Maheshwari; H J Feng; A H Lagrange; J H Shaver; N J Kassebaum; R Venkataraman; F Baudenbacher; R L Macdonald
Journal:  J Neurosci Methods       Date:  2008-10-21       Impact factor: 2.390

7.  Cdk-mediated phosphorylation of the Kvβ2 auxiliary subunit regulates Kv1 channel axonal targeting.

Authors:  Hélène Vacher; Jae-Won Yang; Oscar Cerda; Amapola Autillo-Touati; Bénédicte Dargent; James S Trimmer
Journal:  J Cell Biol       Date:  2011-02-28       Impact factor: 10.539

8.  KV 1/D-type potassium channels inhibit the excitability of bronchopulmonary vagal afferent nerves.

Authors:  Hui Sun; Mayur J Patil; Fei Ru; Sonya Meeker; Bradley J Undem
Journal:  J Physiol       Date:  2022-04-29       Impact factor: 6.228

9.  Mechanism of stress-induced attacks in an episodic neurologic disorder.

Authors:  Heather D Snell; Ariel Vitenzon; Esra Tara; Chris Chen; Jaafar Tindi; Bryen A Jordan; Kamran Khodakhah
Journal:  Sci Adv       Date:  2022-04-20       Impact factor: 14.957

10.  Gene-to-gene interaction between sodium channel-related genes in determining the risk of antiepileptic drug resistance.

Authors:  Sin-Young Jang; Myeong-Kyu Kim; Kee-Ra Lee; Man-Seok Park; Byeong-Chae Kim; Ki-Hyun Cho; Min-Cheol Lee; Yo-Sik Kim
Journal:  J Korean Med Sci       Date:  2009-02-28       Impact factor: 2.153

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