Prevalence of hereditary transthyretin amyloid polyneuropathy in idiopathic progressive neuropathy in conurban areas

BACKGROUND: Hereditary transthyretin amyloidosis (ATTR amyloidosis) is a rare, genetically heterogenous, and clinically variable autosomal dominant disease that severely reduces life expectancy. As treatment options grow, a proper diagnostic approach is mandatory especially in non-endemic regions wi...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Neurol Res Pract
Päätekijät: Thimm, Andreas, Bolz, Saskia, Fleischer, Michael, Stolte, Benjamin, Wurthmann, Sebastian, Totzeck, Andreas, Carpinteiro, Alexander, Luedike, Peter, Papathanasiou, Maria, Rischpler, Christoph, Herrmann, Ken, Rassaf, Tienush, Steinmüller-Magin, Lars, Kleinschnitz, Christoph, Hagenacker, Tim
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2019
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7650113/
https://ncbi.nlm.nih.gov/pubmed/33324896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s42466-019-0035-z
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