Adult-onset vocal cord paralysis in slow-channel congenital myasthenic syndrome.

Autor: Nakamura H; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Komiya H; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Uematsu E; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Nakae Y; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Tanaka K; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Kunii M; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Tada M; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Joki H; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Koyano S; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Matsumoto N; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Doi H; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Takeuchi H; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan., Tanaka F; Department of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Jazyk: angličtina
Zdroj: Neurology. Clinical practice [Neurol Clin Pract] 2019 Oct; Vol. 9 (5), pp. e45-e47.
DOI: 10.1212/CPJ.0000000000000599
Databáze: MEDLINE