Aprataxin mutations are a rare cause of early onset ataxia in Germany

By Habeck Matthias   Zühlke Christine   Bentele Karl   Unkelbach Stephan   Kreß Wolfram   Bürk Katrin   Schwinger Eberhard   Hellenbroich Yorck  

Journal of Neurology, Vol. 251, Iss. 5, 2004-05 ,pp. : 591-594

Springer Publishing Company

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Parkin mutations are frequent in patients with isolated early-onset parkinsonism

By Nicholl D.  

Brain, Vol. 126, Iss. 6, 2003-06 ,pp. : 1271-1278

Oxford University Press

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Is the early-onset torsion dystonia (EOTD) linked to TOR1A gene as frequent as expected in France?

By Frédéric M.  

Neurogenetics, Vol. 9, Iss. 2, 2008-05 ,pp. : 143-150

Springer Publishing Company

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Idiopathic late-onset cerebellar ataxia with cerebellar atrophy in a patient diagnosed with Chiari I malformation: a case report

By Petracca Maria   Cerillo Ilaria   Montella Silvana   Cerullo Giovanni   Carrieri Pietro  

Neurological Sciences, Vol. 34, Iss. 12, 2013-12 ,pp. : 2235-2237

Springer Publishing Company

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Late onset Alexander’s disease presenting as cerebellar ataxia associated with a novel mutation in the gene

By Schmidt Stephan   Wattjes Mike   Gerding Wanda   Knaap Marjo  

Journal of Neurology, Vol. 258, Iss. 5, 2011-05 ,pp. : 938-940

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