Approach to the Differential Diagnosis of Cerebellar Ataxias
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-97911-3_81-2
Reference108 articles.
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2. Anheim M, Fleury M, Monga B et al (2010) Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management. Neurogenetics 11:1–12
3. Anheim M, Tranchant C, Koenig M (2012) The autosomal recessive cerebellar ataxias. N Engl J Med 366:636–646
4. Artuch R, Brea-Calvo G, Briones P et al (2006) Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation. J Neurol Sci 246:153–158
5. Baloh RW, Jen JC (2000) Episodic ataxia type 2 and spinocerebellar ataxia type 6. In: Klockgether T (ed) Handbook of ataxias. Marcel Dekker, New York
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