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  • Print publication year: 2014
  • Online publication date: June 2014

8 - Ataxia, subacute or chronic

from Section 1 - Differential Diagnosis of Abnormal Symptoms and Signs

References

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2. Schöls L, Bauer P, Schmidt T et al. Autosomal dominant cerebellar ataxias: clinical features, genetics and pathogenesis. Lancet Neurol 2004; 3:292–304.
3. Fogel BL, Perlman S. Clinical features and molecular genetics of autosomal recessive cerebellar ataxias. Lancet Neurol 2007; 6:245–57.
4. Anheim M, Tranchant C, Koenig M. The autosomal recessive cerebellar ataxias. N Engl J Med 2012; 366:636–46.
5. Durr A. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. Lancet Neurol 2010; 9:885–94.
6. Subramony SH. Overview of autosomal dominant ataxias. Handb Clin Neurol 2012; 103:389–98.
7. Jen JC, Graves TD, Hess EJ et al. Primary episodic ataxias: diagnosis, pathogenesis and treatment. Brain 2007; 130:2484–93.
8. Leehey MA. Fragile X-associated tremor/ataxia syndrome: clinical phenotype, diagnosis, and treatment. J Investig Med 2009; 57:830–6.
9. Zeviani M, Di Donato S. Mitochondrial disorders. Brain 2004; 12:2153–72.