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Efficacy of salbutamol monotherapy in slow-channel congenital myasthenic syndrome caused by a novel mutation in CHRND.
Tawara, Nozomu; Yamashita, Satoshi; Takamatsu, Koutaro; Yamasaki, Yoshimune; Mukaino, Akihiro; Nakane, Shunya; Farshadyeganeh, Paniz; Ohno, Kinji; Ando, Yukio.
Afiliação
  • Tawara N; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Yamashita S; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Takamatsu K; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Yamasaki Y; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Mukaino A; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Nakane S; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Farshadyeganeh P; Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Ohno K; Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Ando Y; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Muscle Nerve ; 63(4): E30-E32, 2021 04.
Article em En | MEDLINE | ID: mdl-33428214

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Colinérgicos / Síndromes Miastênicas Congênitas / Albuterol / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Colinérgicos / Síndromes Miastênicas Congênitas / Albuterol / Mutação Tipo de estudo: Diagnostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article