|1.||Grateau, Gilles: 2 articles (04/2009 - 01/2006)|
|2.||Hawkins, Philip N: 2 articles (03/2007 - 11/2005)|
|3.||Neerman-Arbez, Marguerite: 1 article (03/2010)|
|4.||de Moerloose, Philippe: 1 article (03/2010)|
|5.||Fish, Richard J: 1 article (03/2010)|
|6.||Abdel Wahab, Magy: 1 article (03/2010)|
|7.||Mourad, Georges: 1 article (04/2009)|
|8.||Delabre, Jean-Philippe: 1 article (04/2009)|
|9.||Le Quellec, Alain: 1 article (04/2009)|
|10.||Pageaux, Georges-Philippe: 1 article (04/2009)|
09/01/2004 - "Immunohistochemical studies revealed AFib amyloidosis and genetic studies the amino acid exchange Glu526Val of the fibrinogen Aalpha-chain mutation, which was also present in one of her sons. "
04/01/2009 - "The predominant cause of hereditary renal amyloidosis is a mutation of the fibrinogen Aalpha chain (AFib), the most common being the E526V mutation. "
07/01/2008 - "Three German fibrinogen Aalpha-chain amyloidosis patients with the p.Glu526Val mutation."
03/01/2006 - "Four mutations in the fibrinogen Aalpha-chain that are able to induce amyloidosis have been identified so far, the most common being the Glu526Val mutation. "
11/01/2005 - "This is the first description of hereditary fibrinogen Aalpha chain amyloidosis in an Asian individual, and the distinctive renal histology offered a strong clue to the diagnosis. "
|2.||Afibrinogenemia (Fibrinogen Deficiency)
03/01/2010 - "Congenital afibrinogenemia is a rare coagulation disorder attributed to over forty mutations found either in homozygosity or in compound heterozygosity, the majority localized in FGA encoding the fibrinogen Aalpha-chain. "
03/01/2005 - "To examine the precise basis for the fibrinogen deficiency, mixtures of any two vectors, the fibrinogen Aalpha-, Bbeta-, gamma- (153Cys) or gammam-(153Ala) chain were transfected into Chinese hamster ovary cells (CHO-Aalpha/gamma, -Aalpha/gammam, -Bbeta/gamma, -Bbeta/gammam). "
07/01/2000 - "Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia."
02/15/2000 - "Although several mutations in the fibrinogen genes associated with dysfibrinogenemia and hypofibrinogenemia have been described, the genetic defects of congenital afibrinogenemia are largely unknown, except for a recently reported 11-kb deletion of the fibrinogen Aalpha-chain gene. "
|3.||Familial Amyloidosis (Hereditary Amyloidosis)
11/01/2005 - "Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene."
03/01/2006 - "Successful hepatorenal transplantation in hereditary amyloidosis caused by a frame-shift mutation in fibrinogen Aalpha-chain gene."
01/01/2006 - "Nonneuropathic amyloidoses (Ostertag type amyloidosis) include those due to abnormalities in lysozyme, fibrinogen Aalpha-chain, and apolipoprotein A-I and A-II. The role of lysozyme in amyloid-related human disorders was first described in 1993; to date, there have been only 9 publications describing this disorder, which is a nonneuropathic form of hereditary amyloidosis. "
|1.||Apolipoprotein A-I (Apolipoprotein A1)
|4.||Blood Proteins (Serum Proteins)
|5.||Apolipoprotein A-II (Apolipoprotein A2)
|6.||Amyloid (Amyloid Fibrils)
|8.||Fibrinogen (Factor I)
|9.||gamma-Glutamyltransferase (gamma-Glutamyl Transpeptidase)
|1.||Transplantation (Transplant Recipients)