Literature DB >> 9642539

The place of migraine as a channelopathy.

L J Ptácek1.   

Abstract

Over the past 8 years an increasing awareness of the role of mutant ion channels in episodic diseases of humans has emerged. The importance of these discoveries is now being extended to a growing list of membrane excitability disorders of the nervous system. Molecular characterization of episodic diseases that are rare and monogenic will ultimately shed light on more common and complex disorders, such as epilepsy and migraine.

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Year:  1998        PMID: 9642539     DOI: 10.1097/00019052-199806000-00005

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  6 in total

1.  Therapy of Migraine Headache in Cancer Patients.

Authors: 
Journal:  Curr Rev Pain       Date:  1999

Review 2.  Animal models of chronic migraine.

Authors:  Robin James Storer; Weera Supronsinchai; Anan Srikiatkhachorn
Journal:  Curr Pain Headache Rep       Date:  2015-01

3.  Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.

Authors:  Robert S Raike; Holly B Kordasiewicz; Randall M Thompson; Christopher M Gomez
Journal:  Mol Cell Neurosci       Date:  2006-12-11       Impact factor: 4.314

Review 4.  Molecular mechanisms of migraine?

Authors:  S V Ramagopalan; N E Ramscar; M Z Cader
Journal:  J Neurol       Date:  2007-11-07       Impact factor: 4.849

5.  The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells.

Authors:  Karim Melliti; Manfred Grabner; Guy R Seabrook
Journal:  J Physiol       Date:  2003-01-15       Impact factor: 5.182

Review 6.  Calcium channels and channelopathies of the central nervous system.

Authors:  Daniela Pietrobon
Journal:  Mol Neurobiol       Date:  2002-02       Impact factor: 5.590

  6 in total

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