Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy.

Millere, Elina; Rots, Dmitrijs; Glazere, Ieva; Taurina, Gita; Kurjane, Natalja; Priedite, Viktorija; Gailite, Linda; Blennow, Kaj; Zetterberg, Henrik; Kenina, Viktorija

Millere, Elina; Rots, Dmitrijs; Glazere, Ieva; Taurina, Gita; Kurjane, Natalja; Priedite, Viktorija; Gailite, Linda; Blennow, Kaj; Zetterberg, Henrik; Kenina, Viktorija.

Afiliação

Millere E; Department of Neurology and Neurosurgery, Children's Clinical University Hospital, Riga, Latvia.
Rots D; Department of Doctoral Studies, Riga Stradins University, Riga, Latvia.
Glazere I; Scientific Laboratory of Molecular Genetics, Riga Stradins University, Riga, Latvia.
Taurina G; Scientific Laboratory of Molecular Genetics, Riga Stradins University, Riga, Latvia.
Kurjane N; Department of Neurology, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Priedite V; Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia.
Gailite L; Department of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.
Blennow K; Department of Biology and Microbiology, Riga Stradins University, Riga, Latvia.
Zetterberg H; Outpatient Service Centre, Pauls Stradins Clinical University Hospital, Riga, Latvia.
Kenina V; BIOCON Medical Laboratory, LCC BIOCON, Riga, Latvia.

Front Neurol ; 11: 586610, 2020.

Article em En | MEDLINE | ID: mdl-33551952

Palavras-chave

Kennedy disease; biomarker; clinical features; neurofilament; phenotype; spinal and bulbar muscular atrophy

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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Letônia