Ragno, M <br/><br/>
Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family.  [electronic resource] 

 -  Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology  Jun 2005 
 - 67-71 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>1590-1874 
<br/><br/><label>Standard No.: </label>10.1007/s10072-005-0438-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Ataxin-1<br/>Ataxins<br/>Electric Stimulation--methods<br/>Electrophysiology--methods<br/>Evoked Potentials, Somatosensory--physiology<br/>Family Health<br/>Female<br/>Follow-Up Studies<br/>Humans<br/>Magnetics<br/>Male<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Neural Conduction--physiology<br/>Nuclear Proteins--genetics<br/>Reaction Time--physiology<br/>Spinocerebellar Ataxias--genetics<br/>Tibial Nerve--physiopathology