|1.||Moro, Elena: 1 article (07/2013)|
|2.||Lang, Anthony E: 1 article (07/2013)|
|3.||Sidiropoulos, Christos: 1 article (07/2013)|
|4.||Seidel, Kay: 1 article (07/2012)|
|5.||Rüb, Udo: 1 article (07/2012)|
|6.||Korf, Horst-Werner: 1 article (07/2012)|
|7.||Siswanto, Sonny: 1 article (07/2012)|
|8.||Brunt, Ewout R P: 1 article (07/2012)|
|9.||den Dunnen, Wilfred: 1 article (07/2012)|
|10.||Zhou, Xin: 1 article (08/2010)|
|1.||Spinocerebellar Ataxias (Spinocerebellar Ataxia)
12/12/2006 - "Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5."
04/01/2006 - "The families that we describe shared some relevant clinical and imagiological features with spinocerebellar ataxia type 5 and the recently described spinocerebellar ataxia type 20, allelic to spinocerebellar ataxia type 5. Spinocerebellar ataxia types 5 and 20 could be different phenotypic expressions of the same molecular disorder. "
|2.||Dysphonia (Spastic Dysphonia)
|4.||Mitochondrial Diseases (Mitochondrial Disease)
07/09/2013 - "Similar diffuse intracranial calcification can be seen in a variety of disorders including idiopathic basal ganglia calcifications and spinocerebellar ataxia 20.(1) Mitochondrial disorders(2) are a well-recognized cause; however, to our knowledge this is the first time that such extensive intracranial calcium deposits have been described in a patient with a POLG1 mutation. "
|5.||Progressive Myoclonic Epilepsies (Progressive Myoclonic Epilepsy)