Literature DB >> 30713863

Holmes-Like Tremor in Ataxia With Oculomotor Apraxia Type 2.

Maria Chiara D'Amico1, Iole Borrelli2, Holta Zhuzhuni2, Aurelio D'Amico2, Roberta Di Giacomo2, Luca Mancinelli2, Valeria di Tommaso2, Antonio Di Muzio2, Marco Onofrj1.   

Abstract

Entities:  

Keywords:  Ataxia with oculomotor apraxia type 2; Holmes‐like tremor; polyneuropathy

Year:  2014        PMID： 30713863      PMCID： PMC6353373          DOI： 10.1002/mdc3.12070

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN： 2330-1619


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  10 in total

1.  Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic study.

Authors:  C Criscuolo; L Chessa; S Di Giandomenico; P Mancini; F Saccà; G S Grieco; M Piane; F Barbieri; G De Michele; S Banfi; F Pierelli; N Rizzuto; F M Santorelli; L Gallosti; A Filla; C Casali
Journal:  Neurology       Date:  2006-04-25       Impact factor: 9.910

2.  Successful treatment of Holmes tremor by levetiracetam.

Authors:  Edoardo Ferlazzo; Francesca Morgante; Vincenzo Rizzo; Giuseppe Sciarrone; Mario Meduri; Adriana Magaudda; Paolo Girlanda; Angelo Quartarone
Journal:  Mov Disord       Date:  2008-10-30       Impact factor: 10.338

3.  Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients.

Authors:  M Tazir; L Ali-Pacha; A M'Zahem; J P Delaunoy; M Fritsch; S Nouioua; T Benhassine; S Assami; D Grid; J M Vallat; A Hamri; M Koenig
Journal:  J Neurol Sci       Date:  2009-01-11       Impact factor: 3.181

Review 4.  Consensus statement of the Movement Disorder Society on Tremor. Ad Hoc Scientific Committee.

Authors:  G Deuschl; P Bain; M Brin
Journal:  Mov Disord       Date:  1998       Impact factor: 10.338

5.  Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.

Authors:  M Anheim; B Monga; M Fleury; P Charles; C Barbot; M Salih; J P Delaunoy; M Fritsch; L Arning; M Synofzik; L Schöls; J Sequeiros; C Goizet; C Marelli; I Le Ber; J Koht; J Gazulla; J De Bleecker; M Mukhtar; N Drouot; L Ali-Pacha; T Benhassine; M Chbicheb; A M'Zahem; A Hamri; B Chabrol; J Pouget; R Murphy; M Watanabe; P Coutinho; M Tazir; A Durr; A Brice; C Tranchant; M Koenig
Journal:  Brain       Date:  2009-08-20       Impact factor: 13.501

6.  Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.

Authors:  Isabelle Le Ber; Naïma Bouslam; Sophie Rivaud-Péchoux; João Guimarães; Ali Benomar; Céline Chamayou; Cyril Goizet; Maria-Ceù Moreira; Sandra Klur; Mohamed Yahyaoui; Yves Agid; Michel Koenig; Giovanni Stevanin; Alexis Brice; Alexandra Dürr
Journal:  Brain       Date:  2004-01-21       Impact factor: 13.501

7.  Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Authors:  Mathieu Anheim; Marie-Celine Fleury; Jerome Franques; Maria-Ceu Moreira; Jean-Pierre Delaunoy; Dominique Stoppa-Lyonnet; Michel Koenig; Christine Tranchant
Journal:  Arch Neurol       Date:  2008-07

8.  Ovarian failure in ataxia with oculomotor apraxia type 2.

Authors:  David R Lynch; Corey D Braastad; Narasimhan Nagan
Journal:  Am J Med Genet A       Date:  2007-08-01       Impact factor: 2.802

9.  Cohort study of prevalence and phenomenology of tremor in dementia with Lewy bodies.

Authors:  Marco Onofrj; Sara Varanese; Laura Bonanni; John-Paul Taylor; Angelo Antonini; Enza Maria Valente; Simona Petrucci; Fabrizio Stocchi; Astrid Thomas; Bernardo Perfetti
Journal:  J Neurol       Date:  2013-02-12       Impact factor: 4.849

10.  SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.

Authors:  Lorenzo Nanetti; Simona Cavalieri; Viviana Pensato; Alessandra Erbetta; Davide Pareyson; Marta Panzeri; Giovanna Zorzi; Carlo Antozzi; Isabella Moroni; Cinzia Gellera; Alfredo Brusco; Caterina Mariotti
Journal:  Orphanet J Rare Dis       Date:  2013-08-14       Impact factor: 4.123
  10 in total

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