Literature DB >> 16145613

Calcium channel "gaiting" and absence epilepsy.

Jeffrey L Noebels.   

Abstract

Entities:  

Year:  2005        PMID： 16145613      PMCID： PMC1198627          DOI： 10.1111/j.1535-7511.2005.05306.x

Source DB:  PubMed          Journal:  Epilepsy Curr        ISSN： 1535-7511            Impact factor:   7.500


× No keyword cloud information.
  13 in total

1.  Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia.

Authors:  Takahito Wada; Norio Kobayashi; Yoshio Takahashi; Tomoko Aoki; Takako Watanabe; Shinji Saitoh
Journal:  Pediatr Neurol       Date:  2002-01       Impact factor: 3.372

2.  The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

Authors:  A Ducros; C Denier; A Joutel; M Cecillon; C Lescoat; K Vahedi; F Darcel; E Vicaut; M G Bousser; E Tournier-Lasserve
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

3.  Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.

Authors:  E S Piedras-Renteria; K Watase; N Harata; O Zhuchenko; H Y Zoghbi; C C Lee; R W Tsien
Journal:  J Neurosci       Date:  2001-12-01       Impact factor: 6.167

4.  Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.

Authors:  Isabel Alonso; José Barros; Assunção Tuna; João Coelho; Jorge Sequeiros; Isabel Silveira; Paula Coutinho
Journal:  Arch Neurol       Date:  2003-04

5.  Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha1A subunit of P/Q type calcium channels.

Authors:  C Ayata; M Shimizu-Sasamata; E H Lo; J L Noebels; M A Moskowitz
Journal:  Neuroscience       Date:  2000       Impact factor: 3.590

6.  Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.

Authors:  O Zhuchenko; J Bailey; P Bonnen; T Ashizawa; D W Stockton; C Amos; W B Dobyns; S H Subramony; H Y Zoghbi; C C Lee
Journal:  Nat Genet       Date:  1997-01       Impact factor: 38.330

7.  Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.

Authors:  S H Subramony; Kelly Schott; Robert S Raike; Joel Callahan; Leigh R Langford; Peka S Christova; John H Anderson; Christopher M Gomez
Journal:  Ann Neurol       Date:  2003-12       Impact factor: 10.422

8.  Mutations in high-voltage-activated calcium channel genes stimulate low-voltage-activated currents in mouse thalamic relay neurons.

Authors:  Yi Zhang; Mayra Mori; Daniel L Burgess; Jeffrey L Noebels
Journal:  J Neurosci       Date:  2002-08-01       Impact factor: 6.167

9.  A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.

Authors:  Arn M J M van den Maagdenberg; Daniela Pietrobon; Tommaso Pizzorusso; Simon Kaja; Ludo A M Broos; Tiziana Cesetti; Rob C G van de Ven; Angelita Tottene; Jos van der Kaa; Jaap J Plomp; Rune R Frants; Michel D Ferrari
Journal:  Neuron       Date:  2004-03-04       Impact factor: 17.173

10.  Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.

Authors:  Angelita Tottene; Tommaso Fellin; Stefano Pagnutti; Siro Luvisetto; Joerg Striessnig; Colin Fletcher; Daniela Pietrobon
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-16       Impact factor: 11.205
View more
  1 in total

Review 1.  T-type Ca2+ channels in absence epilepsy.

Authors:  Eunji Cheong; Hee-Sup Shin
Journal:  Pflugers Arch       Date:  2014-02-13       Impact factor: 3.657
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.