Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin: a comment.

Roteta Unceta Barrenechea, Ana; Aibar Arregui, Miguel Ángel; Andrés Gracia, Alejandro; Melero Polo, Jorge; Lahuerta Pueyo, Carmen; Menao Guillén, Sebastián; Torralba Cabeza, Miguel Ángel

Roteta Unceta Barrenechea, Ana; Aibar Arregui, Miguel Ángel; Andrés Gracia, Alejandro; Melero Polo, Jorge; Lahuerta Pueyo, Carmen; Menao Guillén, Sebastián; Torralba Cabeza, Miguel Ángel.

Afiliação

Roteta Unceta Barrenechea A; Department of Nuclear Medicine, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragón, Spain.
Aibar Arregui MÁ; Department of Cardiology, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
Andrés Gracia A; Department of Nuclear Medicine, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragón, Spain.
Melero Polo J; Department of Cardiology, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
Lahuerta Pueyo C; Department of Clinical Biochemistry, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
Menao Guillén S; Department of Clinical Biochemistry, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
Torralba Cabeza MÁ; Department of Internal Medicine, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.

Amyloid ; 27(2): 144, 2020 06.

Article em En | MEDLINE | ID: mdl-31906714

Assuntos

Neuropatias Amiloides Familiares; Amiloidose Familiar; Humanos; Pré-Albumina

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares / Amiloidose Familiar Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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