fibrinogen has been researched along with Amyloidosis, Familial in 22 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 9 (40.91) | 29.6817 |
| 2010's | 12 (54.55) | 24.3611 |
| 2020's | 1 (4.55) | 2.80 |
| Authors | Studies |
|---|---|
| Azar, R; Bacri, JL; Bobrie, G; Boffa, JJ; Clabault, K; Colombat, M; Ducloux, D; Dürrbach, A; Duvic, C; El Karoui, K; Ferlicot, S; François, H; Garrigue, V; Guerrot, D; Hoffmann, M; Lionet, A; Mansour, J; Meyer, L; Mousson, C; Nochy, D; Panescu, V; Plaisier, E; Ratsimbazafy, A; Ulrich, M; Valleix, S; Vigneau, C; Vrigneaud, L | 1 |
| Beugnet, C; Bridoux, F; Briki, F; Delpech, M; Derreumaux, P; Dogan, A; Doucet, J; Garnier, C; Goude, R; Grateau, G; Le Pogamp, P; Martin, L; Nedelec, B; Rioux-Leclercq, N; Valleix, S | 1 |
| Kametani, F; Okumura, N; Sekijima, Y; Yazaki, M; Yoshinaga, T | 1 |
| Antlanger, M; Gilbertson, JA; Gremmel, T; Haidinger, M; Hawkins, PN; Hecking, M; Hörl, WH; Kain, R; Kopecky, C; Mascherbauer, J; Pfaffenberger, S; Rowczenio, D; Säemann, MD; Weichhart, T; Werzowa, J | 1 |
| Dasari, S; Dogan, A; Highsmith, WE; Kocher, JP; Kurtin, PJ; Theis, JD; Vrana, JA; Zenka, RM; Zimmermann, MT | 1 |
| Cez, A; El Karoui, K; Galmiche, L; Hummel, A; Knebelmann, B | 1 |
| Wang, SX; Yao, Y; Zhang, YK | 1 |
| Hachiya, N; Higuchi, K; Ikeda, S; Kametani, F; Kanizawa, Y; Miyashita, K; Nishio, S; Sekijima, Y; Yazaki, M; Yoshinaga, T | 1 |
| Delabre, JP; Grateau, G; Le Quellec, A; Mourad, G; Pageaux, GP; Raynaud, P | 1 |
| Linke, RP; Picken, MM | 1 |
| Delabre, JP; Garrigue, V; Mourad, G | 1 |
| Banner, NR; Benson, MD; Buxton-Thomas, M; Heaton, ND; Hendry, BM; Liepnieks, JJ; Maccarthy, P; Mathias, CJ; Monaghan, M; O'Grady, J; Portmann, B; Rela, M; Stangou, AJ; Wendon, J | 1 |
| Gillmore, JD; Hawkins, PN; Lachmann, HJ; Wechalekar, A | 1 |
| Ballenger, FJ; Bhola, V; Cathro, H; Kunaparaju, S; Okafor, C; Rosner, MH | 1 |
| Azoulay, D; Benson, MD; Conceicao, I; Ericzon, BG; Grateau, G; Heaton, N; Linke, RP; Lobato, L; O'Grady, J; Otto, G; Picken, M; Portmann, B; Rela, M; Stangou, AJ; Suhr, O; Wilczek, H; Zeldenrust, S | 1 |
| Benson, M; Corrêa, RR; Machado, JR; Neves, PD; Oliveira, FA; Reis, MA; Rodrigues, WV; Silva, MV | 1 |
| Benson, M; Björnsson, J; Gertz, M; Schwab, T; Uemichi, T; Wiesner, R; Zeldenrust, S | 1 |
| Benson, MD | 1 |
| Bybee, A; Cheong, HI; Choi, Y; Gilbertson, JA; Ha, IS; Hawkins, PN; Kang, HG; Park, MS | 1 |
| Heyd, B; Justrabo, E; Miguet, JP; Mousson, C; Rebibou, JM; Rifle, G; Tanter, Y | 1 |
| Bofinger, A; Francis, L; Goodman, HJ; Lane, SW; Mollee, PN | 1 |
| Booth, DR; Booth, SE; Bybee, A; Gilbertson, JA; Gillmore, JD; Hawkins, PN; Lachmann, HJ; Pepys, MB | 1 |
4 review(s) available for fibrinogen and Amyloidosis, Familial
| Article | Year |
|---|---|
Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics.
Topics: Amyloidosis, Familial; Asia; Female; Fibrinogen; Humans; Intestinal Mucosa; Kidney; Male; Mutation; Organ Specificity | 2018 |
[Hereditary fibrinogen Aα-chain amyloidosis caused by the E526V mutation: a case report and literature review].
Topics: Amyloidosis, Familial; Fibrinogen; Humans; Kidney; Kidney Diseases; Male; Mutation; Proteinuria | 2014 |
[A preemptive combined liver-kidney transplantation in Aalpha fibrinogen chain renal amyloidosis].
Topics: Adult; Amyloidosis, Familial; Female; Fibrinogen; Humans; Kidney Failure, Chronic; Kidney Transplantation; Liver Transplantation; Mutation, Missense; Pedigree; Point Mutation; Secondary Prevention | 2009 |
Ostertag revisited: the inherited systemic amyloidoses without neuropathy.
Topics: Amyloidosis, Familial; Apolipoprotein A-I; Apolipoprotein A-II; Diagnosis, Differential; Fibrinogen; Humans; Muramidase; Mutation; Peripheral Nervous System Diseases | 2005 |
18 other study(ies) available for fibrinogen and Amyloidosis, Familial
| Article | Year |
|---|---|
Organ Transplantation in Hereditary Fibrinogen A α-Chain Amyloidosis: A Case Series of French Patients.
Topics: Adolescent; Adult; Aged; Amyloidosis, Familial; Child; Combined Modality Therapy; Disease Progression; Female; Fibrinogen; Follow-Up Studies; Frameshift Mutation; France; Genetic Association Studies; Humans; Kidney; Kidney Failure, Chronic; Kidney Transplantation; Liver Transplantation; Male; Middle Aged; Mutation, Missense; Point Mutation; Renal Dialysis; Treatment Outcome; Young Adult | 2020 |
VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants.
Topics: Amino Acid Motifs; Amino Acid Sequence; Amyloid; Amyloidosis, Familial; Fibrinogen; Frameshift Mutation; Humans; Kidney; Protein Conformation, beta-Strand | 2017 |
Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literature.
Topics: Aged; Amyloid; Amyloidosis, Familial; Cardiovascular Diseases; Female; Fibrinogen; Humans; Kidney Diseases; Kidney Transplantation; Male; Middle Aged; Mutation; Pedigree; Prognosis; Proteinuria; Review Literature as Topic; Spain | 2013 |
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Topics: Aged; Amyloid; Amyloidosis, Familial; Apolipoprotein A-I; Computational Biology; DNA Mutational Analysis; Female; Fibrinogen; Humans; Male; Middle Aged; Mutation; Peptides; Plaque, Amyloid; Proteins; Proteome; Proteomics; Reproducibility of Results; Tandem Mass Spectrometry | 2014 |
Quiz page: a familial glomerulopathy.
Topics: Amyloidosis, Familial; Biopsy; Female; Fibrinogen; Humans; Kidney; Kidney Diseases; Kidney Glomerulus; Middle Aged; Ultrasonography | 2014 |
The first pure form of Ostertag-type amyloidosis in Japan: a sporadic case of hereditary fibrinogen Aα-chain amyloidosis associated with a novel frameshift variant.
Topics: Adult; Amyloidosis, Familial; Exons; Female; Fibrinogen; Frameshift Mutation; Humans; Japan | 2015 |
Nephrotic syndrome due to an amyloidogenic mutation in fibrinogen A alpha chain.
Topics: Amyloid; Amyloidosis, Familial; Female; Fibrinogen; Humans; Kidney; Middle Aged; Nephrotic Syndrome | 2009 |
Cardiac amyloidosis with the E526V mutation of the fibrinogen A alpha-chain.
Topics: Amyloid; Amyloidosis, Familial; Biopsy; Fibrinogen; Heart Diseases; Humans; Immunohistochemistry; Kidney Diseases; Male; Middle Aged; Mutation | 2008 |
Hereditary fibrinogen A alpha-chain amyloidosis: phenotypic characterization of a systemic disease and the role of liver transplantation.
Topics: Adult; Amyloidosis, Familial; Cardiomyopathy, Dilated; Cardiovascular System; Female; Fibrinogen; Humans; Kidney Transplantation; Liver Transplantation; Male; Middle Aged; Mutation; Nervous System Diseases; Patient Selection; Phenotype; Radionuclide Imaging; Technetium Tc 99m Dimercaptosuccinic Acid; Treatment Outcome; Ultrasonography | 2010 |
Hereditary fibrinogen A alpha-chain amyloidosis: clinical phenotype and role of liver transplantation.
Topics: Amyloidosis, Familial; Fibrinogen; Humans; Kidney Failure, Chronic; Kidney Transplantation; Liver Transplantation; Phenotype | 2010 |
Proteinuria in a patient with diabetes.
Topics: Amyloidosis, Familial; Biopsy; Diabetes Mellitus, Type 2; DNA Mutational Analysis; Fibrinogen; Humans; Kidney Diseases; Kidney Glomerulus; Male; Middle Aged; Mutation; Proteinuria | 2011 |
Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses.
Topics: Amyloidosis, Familial; Apolipoprotein A-I; Fibrinogen; Humans; Liver Transplantation; Organ Transplantation; Treatment Outcome | 2012 |
Fibrinogen A alpha-chain amyloidosis: report of the first case in Latin America.
Topics: Amyloid; Amyloidosis, Familial; Brazil; Female; Fibrinogen; Humans; Kidney Glomerulus; Middle Aged; Mutation; Proteinuria | 2013 |
Orthotopic liver transplantation for hereditary fibrinogen amyloidosis.
Topics: Amyloidosis, Familial; Family Health; Fibrinogen; Follow-Up Studies; Humans; Liver Transplantation; Male; Middle Aged | 2003 |
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene.
Topics: Amino Acid Sequence; Amyloidosis, Familial; Asian People; Base Sequence; Child; Female; Fibrinogen; Frameshift Mutation; Gene Deletion; Humans; Korea; Molecular Sequence Data | 2005 |
Successful hepatorenal transplantation in hereditary amyloidosis caused by a frame-shift mutation in fibrinogen Aalpha-chain gene.
Topics: Adult; Amyloidosis, Familial; Biopsy; DNA; Fibrinogen; Follow-Up Studies; Frameshift Mutation; Humans; Kidney Transplantation; Liver Transplantation; Male | 2006 |
Hereditary fibrinogen A alpha-chain amyloidosis.
Topics: Amyloidosis, Familial; Australia; Biopsy; Diagnosis, Differential; DNA; Fibrinogen; Humans; Kidney; Male; Middle Aged; Mutation | 2006 |
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
Topics: Adult; Aged; Amyloidosis; Amyloidosis, Familial; Apolipoprotein A-I; Diagnostic Errors; DNA Mutational Analysis; Female; Fibrinogen; Genotype; Heterozygote; Humans; Kidney; Middle Aged; Muramidase; Paraproteinemias; Point Mutation; Prealbumin; Radionuclide Imaging | 2002 |