| Literature DB >> 11921138 |
Pierre-François Pradat1, François Salachas, Lucette Lacomblez, Nathalie Patte, Nadine Leforestier, Véronique Gaura, Vincent Meininger.
Abstract
Amyotrophic lateral sclerosis (ALS) is classically characterized by the presence of symptoms or signs of upper and lower motor neuron impairment and sparing of other neuronal systems.1 We report on a patient who was primarily diagnosed as typical ALS and developed chorea 10 years after the onset of motor neuron signs. Copyright 2002 Movement Disorder Society.Entities:
Mesh:
Year: 2002 PMID: 11921138 DOI: 10.1002/mds.10039
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338