SM Riad, H Hathout… - American Journal of …, 2011 - Am Soc Neuroradiology PLS is a progressive pure UMN disorder first described in the late 1800s by Charcot and Erb; it can be distinguished from ALS by its characteristic absence of LMN signs. Both conditions arise sporadically, and both have been linked to specific mutations, 1 though PLS is far ... Cited by 2 - Related articles - All 3 versions
MJ Strong, T Hortobágyi, K Okamoto… - … Molecular Pathology of …, 2011 - books.google.com 44 Amyotrophic Lateral Sclerosis, Primary Lateral Sclerosis and Spinal Muscular Atrophy Michael J. Strong1, Tibor Hortobágyi2, Koichi Okamoto3 and Shinsuke Kato4 1 Canada Department of Clinical Neurological Sciences, University ofWestern Ontario, and Robarts Research ...
G Piccolo, E Tavazzi, S Jarius, E Alfonsi… - Neurological …, 2011 - Springer Abstract Anti-Ma2/Ta antibodies are rare paraneoplastic antibodies, which are mostly associated with limbic encephalitis in male patients with testicular cancer. We report on a 50-year-old woman with a pure progressive spastic paraparesis. Next, she was diagnosed as having a ... Related articles - All 2 versions
LC Tzarouchi, AP Kyritsis… - British Journal of …, 2011 - Br Inst Radiology Objective: Primary lateral sclerosis (PLS) is a progressive degenerative disorder affecting upper motor neurons and requires a clinical diagnosis. Diffusion tensor imaging (DTI) is a quantitative method for assessing white matter fibre integrity. The purpose of the study was to ... Related articles - All 3 versions
S Rose, K Pannek, C Bell, F Baumann… - NeuroImage, 2011 - Elsevier ... Fifteen patients with probable or definite ALS as defined by the revised EL Escorial criteria (Brooks et al., 2000) were recruited into the study, see Table 1. These patients were all typical ALS with progressive muscular atrophy and primarylateralsclerosis variants excluded. ...
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