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Ataxia
Citations 1-10 of 68 total displayed.
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Most recent content
(February 6, 2012):
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- Observations
Adult-Onset Vanishing White Matter Disease Due to a Novel EIF2B3 Mutation
- Roberta La Piana; Adeline Vanderver; Marjo van der Knaap; Louise Roux; Donatella Tampieri; Bernard Brais; Geneviève Bernard
Arch Neurol archneurol.2011.1942.
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- Original Contributions
Restricted Diffusion in Vanishing White Matter
- Hannemieke D. W. van der Lei; Marjan E. Steenweg; Marianna Bugiani; Petra J. W. Pouwels; Inge M. Vent; Frederik Barkhof; Wessel N. van Wieringen; Marjo S. van der Knaap
Arch Neurol archneurol.2011.1658.
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Past content
(since July 1998):
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- Images in Neurology
Topiramate Effect in Opsoclonus-Myoclonus-Ataxia Syndrome
- Thiago Dias Fernandes; Rodrigo Bazan; Luiz Eduardo Betting; Fernando Coronetti Gomes da Rocha
Arch Neurol 2012; 69: 133.
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- Observations
Use of Acetazolamide in Sulfonamide-Allergic Patients With Neurologic Channelopathies
- Daniel Platt; Robert C. Griggs
Arch Neurol archneurol.2011.2723.
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- Original Contributions
The APOE  2 Allele Increases the Risk of Earlier Age at Onset in Machado-Joseph Disease
- Conceição Bettencourt; Mafalda Raposo; Nadiya Kazachkova; Teresa Cymbron; Cristina Santos; Teresa Kay; João Vasconcelos; Patrícia Maciel; Karina C. Donis; Maria Luiza Saraiva-Pereira; Laura B. Jardim; Jorge Sequeiros; Manuela Lima
Arch Neurol 2011; 68: 1580-1583.
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- Observations
Postvaccination Miller Fisher Syndrome
- Ashkan Shoamanesh; Kristine Chapman; Anthony Traboulsee
Arch Neurol 2011; 68: 1327-1329.
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- Images in Neurology
Idiopathic Superficial Siderosis
- Thiago Cardoso Vale; Rodrigo Santiago Gomez; Antônio Lúcio Teixeira
Arch Neurol 2011; 68: 1334-1335.
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- Original Contributions
Clinical Characterization of a Kindred With a Novel 12-Octapeptide Repeat Insertion in the Prion Protein Gene
- Neeraj Kumar; Bradley F. Boeve; Brendon P. Boot; Carolyn F. Orr; Joseph Duffy; Bryan K. Woodruff; Anil K. Nair; Jay Ellison; Karen Kuntz; Kejal Kantarci; Clifford R. Jack Jr; Barbara F. Westmoreland; Julie A. Fields; Matthew Baker; Rosa Rademakers; Joseph E. Parisi; Dennis W. Dickson
Arch Neurol 2011; 68: 1165-1170.
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- Observations
Neuropathy in a Human Without the PMP22 Gene
- Mario Andre Saporta; Istvan Katona; Xuebao Zhang; Helen P. Roper; Louise McClelland; Fiona Macdonald; Louise Brueton; Julian Blake; Ueli Suter; Mary M. Reilly; Michael E. Shy; Jun Li
Arch Neurol 2011; 68: 814-821.
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- Original Contributions
SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia
- Cecilia Marelli; Joyce van de Leemput; Janel O. Johnson; Francois Tison; Christel Thauvin-Robinet; Fabienne Picard; Christine Tranchant; Dena G. Hernandez; Bernard Huttin; Jacques Boulliat; Iban Sangla; Christian Marescaux; Serge Brique; Hélène Dollfus; Sampath Arepalli; Isabelle Benatru; Elisabeth Ollagnon; Sylvie Forlani; John Hardy; Giovanni Stevanin; Alexandra Dürr; Andrew Singleton; Alexis Brice
Arch Neurol 2011; 68: 637-643.
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