Clinical features of TTR-FAP in Portugal
Author:
Affiliation:
1. Department of Neurosciences, Centro Hospitalar Lisboa Norte, Hospital de Santa Maria, Lisbon, Portugal
2. Neuromuscular Unit, Instituto de Medicina Molecular, Faculty of Medicine, University of Lisbon, Lisbon, Portugal
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
https://www.tandfonline.com/doi/pdf/10.3109/13506129.2012.673184
Reference16 articles.
1. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).
2. Transthyretin mutations in hyperthyroxinemia and amyloid diseases
3. FAMILIAL AMYLOID POLYNEUROPATHY: AN ELECTRON MICROSCOPE STUDY OF THE PERIPHERAL NERVE IN FIVE CASES. I. INTERSTITIAL CHANGES
4. Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)
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