Clifton L Gooch, Seth L Pullman, Dikoma C Shungu, Aziz M Uluğ, Stephen Chane, Paul H Gordon, Ming X Tang, Xiangling Mao, Lewis P Rowland, Hiroshi Mitsumoto
We prospectively studied 64 patients with motor neuron disease (amyotrophic lateral sclerosis (ALS), familial ALS (fALS), progressive muscular atrophy (PMA) and primary lateral sclerosis (PLS)) using multiple point stimulation motor unit number estimation (MUNE), transcranial magnetic stimulation (TMS), proton magnetic resonance spectroscopic imaging (1H MRSI), diffusion tensor imaging (MRDTI), and clinical measures at baseline and every 3 months thereafter for 15 months. Substantial differences in MUNE were noted among the motor neuron disease subgroups (P = 0...
2009: Supplements to Clinical Neurophysiology