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We describe a long-survival patient carrying heterozygous D90A mutation of SOD1 gene who presented the onset of ALS with severe laryngospasm due to bilateral vocal cord paralysis. We report all the clinical and paraclinical data in the text. Here we are reporting longitudinal EMG data (sensory-motor nerve conduction studies; needle EMG of bulbar, cervical, thoracic, lumbosacral muscles; magnetic stimulation) of patient during the follow up at IRCCS Mondino Foundation.
Funding: Ricerca Corrente 2020 - Ministry of Health (Italy)
laryngospasm, Amyotrophic Lateral Sclerosis, Case report, SOD1, D90A
laryngospasm, Amyotrophic Lateral Sclerosis, Case report, SOD1, D90A
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