Literature DB >> 9750930

Rapid-onset dystonia-parkinsonism: a report of clinical, biochemical, and genetic studies in two families.

A Brashear1, I J Butler, L J Ozelius, P I Kramer, M R Farlow, X O Breakefield, W B Dobyns.   

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Year:  1998        PMID： 9750930

Source DB:  PubMed          Journal:  Adv Neurol        ISSN： 0091-3952


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  5 in total

1.  Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

Authors:  Mark P DeAndrade; Fumiaki Yokoi; Thomas van Groen; Jerry B Lingrel; Yuqing Li
Journal:  Behav Brain Res       Date:  2010-09-17       Impact factor: 3.332

Review 2.  Rare causes of dystonia parkinsonism.

Authors:  Susanne A Schneider; Kailash P Bhatia
Journal:  Curr Neurol Neurosci Rep       Date:  2010-11       Impact factor: 5.081

Review 3.  ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

Authors:  Allison Brashear; Jonathan W Mink; Deborah F Hill; Niki Boggs; W Vaughn McCall; Mark A Stacy; Beverly Snively; Laney S Light; Kathleen J Sweadner; Laurie J Ozelius; Leslie Morrison
Journal:  Dev Med Child Neurol       Date:  2012-08-28       Impact factor: 5.449

4.  Na+/K+ ATPase α1 and α3 isoforms are differentially expressed in α- and γ-motoneurons.

Authors:  Ian J Edwards; Gareth Bruce; Charlotte Lawrenson; Laura Howe; Steven J Clapcote; Susan A Deuchars; Jim Deuchars
Journal:  J Neurosci       Date:  2013-06-12       Impact factor: 6.167

Review 5.  Distinct neurological disorders with ATP1A3 mutations.

Authors:  Erin L Heinzen; Alexis Arzimanoglou; Allison Brashear; Steven J Clapcote; Fiorella Gurrieri; David B Goldstein; Sigurður H Jóhannesson; Mohamad A Mikati; Brian Neville; Sophie Nicole; Laurie J Ozelius; Hanne Poulsen; Tsveta Schyns; Kathleen J Sweadner; Arn van den Maagdenberg; Bente Vilsen
Journal:  Lancet Neurol       Date:  2014-05       Impact factor: 44.182
  5 in total

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