Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis
Author:
Publisher
BMJ
Subject
Psychiatry and Mental health,Clinical Neurology,Surgery
Reference17 articles.
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2. Fosmn: facial onset sensory motor neuronopathy. A ‘benign’ differential diagnosis to bulbar onset motor neuron disease. The first cohort from the UK;Ziso;J Neurol Neurosurg Psychiatry,2013
3. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature;Sonoda;J Neurol Sci,2013
4. FOSMN syndrome: novel insight into disease pathophysiology;Vucic;Neurology,2012
5. Facial onset sensory motor neuronopathy: an immunoglobulin-responsive case;Knopp;J Clin Neuromuscul Dis,2013
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1. Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis;CNS Neuroscience & Therapeutics;2023-03-27
2. Facial onset sensory and motor neuronopathy (FOSMN syndrome): Cases series and systematic review;Neurological Sciences;2023-03-03
3. Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-01-17
4. Sensory Involvement in Amyotrophic Lateral Sclerosis;International Journal of Molecular Sciences;2022-12-08
5. Facial Onset Sensory and Motor Neuronopathy-Like Syndrome: A Case Report;Journal of Clinical Neuromuscular Disease;2022-09
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