المؤلفون: Lorenzoni PJ; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil. lorenzoni@ufpr.br., Giugno VR; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil., Ducci RD; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil., Werneck LC; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil., Kay CSK; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil., Scola RH; Service of Neuromuscular Disorders, Division of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná (UFPR), Curitiba, 80060-900, Brazil.

المصدر: Acta neurologica Belgica [Acta Neurol Belg] 2023 Aug; Vol. 123 (4), pp. 1655-1657. Date of Electronic Publication: 2023 Feb 25.

نوع المنشور: Letter

بيانات الدورية: Publisher: Springer Country of Publication: Italy NLM ID: 0247035 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2240-2993 (Electronic) Linking ISSN: 03009009 NLM ISO Abbreviation: Acta Neurol Belg Subsets: MEDLINE

مواضيع طبية MeSH: Amyloid Neuropathies, Familial*/diagnosis , Amyloid Neuropathies, Familial*/genetics , Polyneuropathies*/diagnosis , Polyneuropathies*/genetics, Humans ; Prealbumin/genetics ; Mutation ; Genetic Testing ; Diagnostic Errors ; Amyloid/genetics ; Amyloid/metabolism

SCR Disease Name: Amyloidosis, Hereditary, Transthyretin-Related