Advanced search
Publication Cover
Amyloid
The Journal of Protein Folding Disorders
Volume 11, 2004 - Issue 3
Submit an article Journal homepage
57
Views
20
CrossRef citations to date
0
Altmetric
Case Report

Mutant fibrinogen A-α-chain associated with hereditary renal amyloidosis and peripheral neuropathy

Mamede de Carvalho Department of Neurology, Hospital de Santa Maria, Lisbon, Portugal; Laboratory of EMG. Centro de Estudos Egas Moniz, Faculty of Medicine, Institute for Molecular Medicine, University of Lisbon, PortugalCorrespondence[email protected]
,
Reinhold P Linke Max-Planck-Institute of Biochemistry, Martinsried, Germany
,
Fernando Domingos Department of Nephrology, Hospital de Santa Maria, Lisbon, Portugal
,
Teresinha Evangelista Department of Neurology, Hospital de Santa Maria, Lisbon, Portugal
,
José Luís Ducla-Soares Department of Medicine III, Hospital de Santa Maria, Lisbon, Portugal
,
Walter BJ Nathrath Institute of Pathology, City-Hospital Harlaching, Munich, Germany
,
Conceição Azevedo-Coutinho Department of Cardiology, Hospital de Santa Maria, Lisbon, Portugal
,
Raquel Lima Molecular Neurobiology, Institute of Molecular Biology and ICBAS, University of Porto, Portugal
&
Maria João Saraiva Molecular Neurobiology, Institute of Molecular Biology and ICBAS, University of Porto, Portugal
 show all
Pages 200-207 | Received 28 Jan 2004, Accepted 14 May 2004, Published online: 06 Jul 2009

Citations (20)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

Isabel Tavares, Márcia E. Oliveira, Nuno Maia, Luciana Moreira, Pedro Castro Lacerda, Josefina Santos, Rosário Santos, Paulo Pinho Costa & Luísa Lobato. (2019) Haplotype analysis of newly diagnosed Portuguese and Brazilian families with fibrinogen amyloidosis caused by the FGA p.Glu545Val variant. Amyloid 26:sup1, pages 144-145.
Read now
I. Tavares, L. Lobato, L. Moreira, J. Santos, P. Lacerda, J. Pinheiro & P. Costa. (2011) Long-term follow-up of patients with hereditary fibrinogen A alpha-chain amyloidosis. Amyloid 18:sup1, pages 221-222.
Read now

Articles from other publishers (18)

Laura E. Biederman, Alana D. Dasgupta, Darren E. Dreyfus, Tibor Nadasdy, Anjali A. Satoskar & Sergey V. Brodsky. (2023) Kidney Biopsy Corner: Amyloidosis. Glomerular Diseases, pages 165-177.
Crossref
Isabel Tavares, João Paulo Oliveira, Ana Pinho, Luciana Moreira, Liliana Rocha, Josefina Santos, Joaquim Pinheiro, Paulo Pinho Costa & Luísa Lobato. (2017) Unrecognized Fibrinogen A α-Chain Amyloidosis: Results From Targeted Genetic Testing. American Journal of Kidney Diseases 70:2, pages 235-243.
Crossref
Samih H. Nasr, Surendra Dasari, Linda Hasadsri, Jason D. Theis, Julie A. Vrana, Morie A. Gertz, Prasuna Muppa, Michael T. Zimmermann, Karen L. Grogg, Angela Dispenzieri, Sanjeev Sethi, W. Edward Highsmith, Giampaolo Merlini, Nelson Leung & Paul J. Kurtin. (2017) Novel Type of Renal Amyloidosis Derived from Apolipoprotein-CII. Journal of the American Society of Nephrology 28:2, pages 439-445.
Crossref
Vishwanath Sivalingam & Basant K. Patel. (2016) Familial mutations in fibrinogen Aα (FGA) chain identified in renal amyloidosis increase in vitro amyloidogenicity of FGA fragment. Biochimie 127, pages 44-49.
Crossref
. 2016. Diagnostic Pathology: Kidney Diseases. Diagnostic Pathology: Kidney Diseases 250 251 .
Isabel Tavares, Luísa Lobato, Carlos Matos, Josefina Santos, Paul Moreira, Maria João Saraiva & António Castro Henriques. (2015) Homozygosity for the E526V Mutation in Fibrinogen A Alpha-Chain Amyloidosis: The First Report. Case Reports in Nephrology 2015, pages 1-6.
Crossref
Adam J. Loavenbruck, Vinay Chaudhry, Steven R. Zeldenrust, Robert J. Spinner, Jason D. Theis & Christopher J. Klein. (2012) Mass spectrometry analysis reveals non-mutated apolipoprotein a1 lumbosacral radiculoplexus amyloidoma. Muscle & Nerve 46:5, pages 817-822.
Crossref
Reinhold P. Linke. (2012) On Typing Amyloidosis Using Immunohistochemistry. Detailled Illustrations, Review and a Note on Mass Spectrometry. Progress in Histochemistry and Cytochemistry 47:2, pages 61-132.
Crossref
. (2011) Abstracts. Amyloid 18:Suppl. 1, pages 6-238.
Crossref
Arie J. Stangou, Nicholas R. Banner, Bruce M. Hendry, Mohamed Rela, Bernard Portmann, Julia Wendon, Mark Monaghan, Philip MacCarthy, Muriel Buxton-Thomas, Christopher J. Mathias, Juris J. Liepnieks, John O'Grady, Nigel D. Heaton & Merrill D. Benson. (2010) Response: Hereditary fibrinogen A α-chain amyloidosis: phenotypic characterization and the role of liver transplantation. Blood 115:21, pages 4314-4315.
Crossref
Arie J. StangouNicholas R. BannerBruce M. HendryMohamed RelaBernard PortmannJulia WendonMark MonaghanPhilip MacCarthyMuriel Buxton-ThomasChristopher J. Mathias, Juris J. Liepnieks, John O'GradyNigel D. HeatonMerrill D. Benson. (2010) Hereditary fibrinogen A α-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation. Blood 115:15, pages 2998-3007.
Crossref
Jean-Philippe Delabre, Georges-Philippe Pageaux, Alain Le Quellec, Pierre Raynaud, Gilles Grateau & Georges Mourad. (2009) Transplantation préemptive foie-rein pour une amylose rénale à fibrinogène Aα. Néphrologie & Thérapeutique 5:2, pages 139-143.
Crossref
Magdalena Eriksson, Stefan Schönland, Raoul Bergner, Ute Hegenbart, Peter Lohse, Hartmut Schmidt & Christoph Röcken. (2008) Three German fibrinogen Aα-chain amyloidosis patients with the p.Glu526Val mutation. Virchows Archiv 453:1, pages 25-31.
Crossref
G Syré, K Altland, S Hargassner, R Linke & G Biesenbach. 2007. XIth International Symposium on Amyloidosis. XIth International Symposium on Amyloidosis 136 138 .
B. BOUMA, C. MAAS, B.P.C. HAZENBERG, H.M. LOKHORST & M.F.B.G. GEBBINK. (2007) Increased plasmin‐α2‐antiplasmin levels indicate activation of the fibrinolytic system in systemic amyloidoses. Journal of Thrombosis and Haemostasis 5:6, pages 1139-1142.
Crossref
Glenys A. TennentStephen O. BrennanArie J. Stangou, John O'Grady, Philip N. HawkinsMark B. Pepys. (2006) Human plasma fibrinogen is synthesized in the liver. Blood 109:5, pages 1971-1974.
Crossref
Reinhold P. Linke, Rosl Oos, Natalie M. Wiegel & Walter B.J. Nathrath. (2006) Classification of amyloidosis: misdiagnosing by way of incomplete immunohistochemistry and how to prevent it. Acta Histochemica 108:3, pages 197-208.
Crossref
Reinhold P. Linke. 2006. Protein Misfolding, Aggregation, and Conformational Diseases. Protein Misfolding, Aggregation, and Conformational Diseases 239 276 .

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.