fibrinogen has been researched along with Atypical Hemolytic-Uremic Syndrome in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 5 (71.43) | 24.3611 |
| 2020's | 2 (28.57) | 2.80 |
| Authors | Studies |
|---|---|
| Bakker, B; Blom, AM; de Breuk, A; de Jong, EK; de Jong, S; den Hollander, AI; Hoyng, CB; Nilsson, SC; van den Heuvel, LP; van der Kar, NCAJ; Volokhina, EB | 1 |
| Dixon, BP; Meir, K; Nitzan-Luques, A; Slae, M; Volovelsky, O; Zugayar, D | 1 |
| Alberti, M; Bresin, E; Caprioli, J; Fremeaux-Bacchi, V; Goodship, TH; Noris, M; Pinto, S; Remuzzi, G; Ribes, D; Rodriguez de Cordoba, S; Rurali, E; Sanchez-Corral, P; Valoti, E | 1 |
| Józsi, M; López-Trascasa, M; Nozal, P; Prohászka, Z; Reuter, S; Sánchez-Corral, P; Uzonyi, B | 1 |
| Harris, CL; Heurich, M; Llorca, O; López-Perrote, A; López-Trascasa, M; Martínez-Barricarte, R; Morgan, BP; Pinto, S; Rodríguez de Córdoba, S; Sánchez-Corral, P; Tortajada, A | 1 |
| Dragon-Durey, MA; Fakhouri, F; Frémeaux-Bacchi, V; Loirat, C; Roumenina, L | 1 |
| Bridoux, F; Cassuto, E; Chatelet, V; Delahousse, M; Frémeaux-Bacchi, V; Jablonski, M; Kamar, N; Le Quintrec, M; Lionet, A; Loirat, C; Moulin, B; Mourad, G; Mousson, C; Rondeau, E; Zuber, J | 1 |
1 review(s) available for fibrinogen and Atypical Hemolytic-Uremic Syndrome
| Article | Year |
|---|---|
Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome.
Topics: Atypical Hemolytic Uremic Syndrome; Autoantibodies; Complement C3-C5 Convertases; Complement C3b; Complement Factor B; Complement Factor H; Complement System Proteins; Fibrinogen; Gene Expression; Glomerulonephritis, IGA; Humans | 2014 |
6 other study(ies) available for fibrinogen and Atypical Hemolytic-Uremic Syndrome
| Article | Year |
|---|---|
Effect of rare coding variants in the CFI gene on Factor I expression levels.
Topics: Aged; Aged, 80 and over; Alleles; Atypical Hemolytic Uremic Syndrome; Complement Factor I; Female; Fibrinogen; Gene Expression Regulation; Genetic Predisposition to Disease; Genotype; Heterozygote; Humans; Macular Degeneration; Male; Middle Aged; Polymorphism, Single Nucleotide | 2020 |
Neonatal thrombotic microangiopathy secondary to factor I variant with Hirschsprung disease.
Topics: Atypical Hemolytic Uremic Syndrome; Fibrinogen; Hirschsprung Disease; Humans; Infant; Infant, Newborn; Kidney; Thrombotic Microangiopathies | 2021 |
Combined complement gene mutations in atypical hemolytic uremic syndrome influence clinical phenotype.
Topics: Adult; Atypical Hemolytic Uremic Syndrome; Child; Child, Preschool; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Female; Fibrinogen; Genetic Association Studies; Haplotypes; Hemolytic-Uremic Syndrome; Humans; Infant; Male; Membrane Cofactor Protein; Middle Aged; Mutation; Pedigree; Penetrance; Risk Factors; Young Adult | 2013 |
The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome.
Topics: Adolescent; Adult; Atypical Hemolytic Uremic Syndrome; Base Sequence; Binding Sites; Child; Complement C3; Complement Factor H; Female; Fibrinogen; Gene Expression; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Membrane Cofactor Protein; Models, Molecular; Molecular Sequence Data; Mutation; Protein Binding; Protein Structure, Tertiary; Proteolysis; Recombinant Proteins; Severity of Illness Index | 2015 |
[Atypical hemolytic-uremic syndrome related to abnormalities within the complement system].
Topics: Atypical Hemolytic Uremic Syndrome; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Fibrinogen; Hemolytic-Uremic Syndrome; Humans; Immunologic Factors; Membrane Cofactor Protein; Mutation; Plasma Exchange; Risk Factors; Treatment Outcome | 2011 |
Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome.
Topics: Adolescent; Adult; Aged; Atypical Hemolytic Uremic Syndrome; Biomarkers; Complement C3; Complement Factor B; Complement Factor H; Complement System Proteins; Female; Fibrinogen; Genetic Testing; Graft Rejection; Graft Survival; Hemolytic-Uremic Syndrome; Humans; Kidney Transplantation; Male; Membrane Cofactor Protein; Middle Aged; Mutation; Prognosis; Recurrence; Retrospective Studies; Risk Factors; Young Adult | 2013 |