Literature DB >> 24371031

Genetics of ataxias: hereditary forms.

N Tirada1, L M Levy2.   

Abstract

Entities:  

Year:  2013        PMID： 24371031      PMCID： PMC7966293          DOI： 10.3174/ajnr.A3783

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN： 0195-6108            Impact factor:   3.825


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  14 in total

Review 1.  Recent advances in the genetics of cerebellar ataxias.

Authors:  Anna Sailer; Henry Houlden
Journal:  Curr Neurol Neurosci Rep       Date:  2012-06       Impact factor: 5.081

2.  Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.

Authors:  Jörg B Schulz; Johannes Borkert; Stefanie Wolf; Tanja Schmitz-Hübsch; Maryla Rakowicz; Caterina Mariotti; Ludger Schöls; Ludger Schoels; Dagmar Timmann; Bart van de Warrenburg; Alexandra Dürr; Massimo Pandolfo; Jun-Suk Kang; Andrés González Mandly; Thomas Nägele; Marina Grisoli; Romana Boguslawska; Peter Bauer; Thomas Klockgether; Till-Karsten Hauser
Journal:  Neuroimage       Date:  2009-07-22       Impact factor: 6.556

3.  Magnetic resonance imaging in spinocerebellar ataxias.

Authors:  Susanne Döhlinger; Till-Karsten Hauser; Johannes Borkert; Andreas R Luft; Jörg B Schulz
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

Review 4.  Update on degenerative ataxias.

Authors:  Thomas Klockgether
Journal:  Curr Opin Neurol       Date:  2011-08       Impact factor: 5.710

5.  Classification of the hereditary ataxias and paraplegias.

Authors:  A E Harding
Journal:  Lancet       Date:  1983-05-21       Impact factor: 79.321

Review 6.  The wide spectrum of spinocerebellar ataxias (SCAs).

Authors:  Mario-Ubaldo Manto
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

7.  Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.

Authors:  L Guerrini; F Lolli; A Ginestroni; G Belli; R Della Nave; C Tessa; S Foresti; M Cosottini; S Piacentini; F Salvi; R Plasmati; D De Grandis; G Siciliano; A Filla; M Mascalchi
Journal:  Brain       Date:  2004-07-07       Impact factor: 13.501

Review 8.  Pharmacological protein targets in polyglutamine diseases: mutant polypeptides and their interactors.

Authors:  Boris A Margulis; Vladimir Vigont; Vladimir F Lazarev; Elena V Kaznacheyeva; Irina V Guzhova
Journal:  FEBS Lett       Date:  2013-05-15       Impact factor: 4.124

9.  Magnetic resonance imaging in hereditary and idiopathic ataxia.

Authors:  U Wüllner; T Klockgether; D Petersen; T Naegele; J Dichgans
Journal:  Neurology       Date:  1993-02       Impact factor: 9.910

Review 10.  Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

Authors:  Ludger Schöls; Peter Bauer; Thorsten Schmidt; Thorsten Schulte; Olaf Riess
Journal:  Lancet Neurol       Date:  2004-05       Impact factor: 44.182
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  1 in total

1.  Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.

Authors:  Laurence Gauquelin; Taila Hartley; Mark Tarnopolsky; David A Dyment; Bernard Brais; Michael T Geraghty; Martine Tétreault; Sohnee Ahmed; Samantha Rojas; Karine Choquet; Jacek Majewski; François Bernier; Allan Micheil Innes; Guy Rouleau; Oksana Suchowersky; Kym M Boycott; Grace Yoon
Journal:  Mov Disord Clin Pract       Date:  2020-09-29
  1 in total

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