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T1 hyperintense focus in the parasagittal anterior left frontal lobe that measures 2.1 x 2.9 cm ). (Contributed by Dr. Daniel Guillaume.)
Jan. 16, 2021
Patients with anti-MAG neuropathy typically have an insidiously progressive, distal and symmetrical, sensory or sensorimotor neuropathy. The disorder usually afflicts men over the age of 60 years. Initial features include acral numbness, paresthesias, reduced proprioception, and Romberg sign. Sensory ataxia occurs in half of the cases and often is the most disabling symptom.
Jan. 05, 2021
Neuro-Ophthalmology & Neuro-Otology
Oct. 21, 2020
Sep. 30, 2020
Immune-mediated cerebellar ataxias are divided in paraneoplastic and nonparaneoplastic diseases. The latter include gluten ataxia, postinfectious cerebellitis, opsoclonus myoclonus ataxia syndrome, anti-GAD ataxia, and primary autoimmune cerebellar ataxia. Nonparaneoplastic immune-mediated cerebellar ataxias are characterized by subacute onset, frequent autoimmune disease history in the patient or relatives, and predominant gait ataxia, usually associated with autoantibodies.
Aug. 28, 2020
Oct. 31, 2020
Feb. 13, 2020
Oct. 13, 2020