Associated Papers
Hereditary Amyloidosis: Insights Into a Fibrinogen A Variant Protein.
Cattaneo ER et al.
Proteins, 2024
Fibrinogen A Alpha-Chain Amyloidosis Associated With a Novel Variant in a Chinese Family.
Jin S et al.
Kidney International Reports, 2021
Fibrinogen alpha amyloidosis: insights from proteomics.
Chapman J et al.
Expert Review of Proteomics, 2019
Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics.
Yazaki M et al.
International Journal of Molecular Sciences, 2018
Unrecognized Fibrinogen A α-Chain Amyloidosis: Results From Targeted Genetic Testing.
Tavares I et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation, 2017
Homozygosity for the E526V Mutation in Fibrinogen A Alpha-Chain Amyloidosis: The First Report.
Tavares I et al.
Case Reports in Nephrology, 2015
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Dasari S et al.
Journal of Proteome Research, 2014
24650283 (PubMed )
Supplement: pr4011475_si_001.pdf
Congenital fibrinogen disorders: an update.
de Moerloose P et al.
Seminars in Thrombosis and Hemostasis, 2013
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