Literature DB >> 23419578

Early clinical features differentiate cerebellar variant MSA and sporadic ataxia.

Alexandra Lloyd-Smith1, Patrizio Jacova, Michael Schulzer, Sian D Spacey.   

Abstract

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Mesh：

Year:  2013        PMID： 23419578     DOI： 10.1017/s0317167100013834

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN： 0317-1671            Impact factor:   2.104


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  3 in total

1.  A Review on the Clinical Diagnosis of Multiple System Atrophy.

Authors:  Iva Stankovic; Alessandra Fanciulli; Victoria Sidoroff; Gregor K Wenning
Journal:  Cerebellum       Date:  2022-08-19       Impact factor: 3.648

2.  Large-scale mitochondrial DNA deletion underlying familial multiple system atrophy of the cerebellar subtype.

Authors:  Abdulaziz Alsemari; Hindi Nasser Al-Hindi
Journal:  Clin Case Rep       Date:  2015-11-23

Review 3.  The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy.

Authors:  Gregor K Wenning; Iva Stankovic; Luca Vignatelli; Alessandra Fanciulli; Giovanna Calandra-Buonaura; Klaus Seppi; Jose-Alberto Palma; Wassilios G Meissner; Florian Krismer; Daniela Berg; Pietro Cortelli; Roy Freeman; Glenda Halliday; Günter Höglinger; Anthony Lang; Helen Ling; Irene Litvan; Phillip Low; Yasuo Miki; Jalesh Panicker; Maria Teresa Pellecchia; Niall Quinn; Ryuji Sakakibara; Maria Stamelou; Eduardo Tolosa; Shoji Tsuji; Tom Warner; Werner Poewe; Horacio Kaufmann
Journal:  Mov Disord       Date:  2022-04-21       Impact factor: 9.698
  3 in total

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