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Congenital myasthenic syndromes in the Thai population: Clinical findings and novel mutations.
Pattrakornkul, Nalinee; Ittiwut, Chupong; Boonsimma, Ponghatai; Boonyapisit, Kanokwan; Khongkhatithum, Chaiyos; Sanmaneechai, Oranee; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk.
Afiliación
  • Pattrakornkul N; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Ittiwut C; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
  • Boonsimma P; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
  • Boonyapisit K; Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Khongkhatithum C; Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
  • Sanmaneechai O; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand. Electronic address: oranee.saan@mahidol.ac.th.
  • Suphapeetiporn K; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
  • Shotelersuk V; Center of Excellence for Medical Genomics, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; Excellence Center for Genomics and Precision Medicine, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand.
Neuromuscul Disord ; 30(10): 851-858, 2020 10.
Article en En | MEDLINE | ID: mdl-32978031
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndromes Miasténicos Congénitos Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Tailandia
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndromes Miasténicos Congénitos Tipo de estudio: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Tailandia