arginine has been researched along with Benign Paroxysmal Peritonitis 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 | 5 (71.43) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Annibal, A; Antebi, A; Braumann, M; Göbel, H; Kubacki, T; Laasch, V; Laboy, R; Müller, RU; Späth, MR; Steiner, JD | 1 |
| Beyazıt, Y; Cetındaglı, I; Hancerlı, Y; Hıra, S; Kara, K; Kara, M; Ozalper, V; Ozturker, C; Tanoglu, A; Yazgan, Y | 1 |
| Celik, S; Kucukardali, Y; Nalbant, S; Oktenli, C; Ozgurtas, T; Sahan, B; Sanisoglu, YS; Sayan, O; Solmazgul, E; Tapan, S; Terekeci, HM; Top, C | 1 |
| Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pellkofer, H; Pöllmann, W | 1 |
| Arici, M; Bakkaloglu, A; Berdeli, A; Besbas, N; Kutlay, S; Ozen, S; Türel, B; Yalcinkaya, F; Yilmaz, E | 1 |
| Fujikawa, S; Hara, M; Kawaguchi, Y; Otani, T; Sugiura, T; Takagi, K | 1 |
| Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pöllmann, W; Rübsamen, H | 1 |
7 other study(ies) available for arginine and Benign Paroxysmal Peritonitis
| Article | Year |
|---|---|
A novel TNFRSF1A mutation associated with TNF-receptor-associated periodic syndrome and its metabolic signature.
Topics: Amyloidosis; Arginine; Cysteine; Familial Mediterranean Fever; Humans; Methionine; Mutation; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Tryptophan | 2023 |
Evaluation of endothelial dysfunction in patients with familial Mediterranean fever: the relationship between the levels of asymmetric dimethylarginine and endocan with carotid intima-media thickness and endothelium-dependent vasodilation.
Topics: Adult; Arginine; Atherosclerosis; Biomarkers; Carotid Intima-Media Thickness; Case-Control Studies; Endothelium, Vascular; Familial Mediterranean Fever; Female; Humans; Inflammation; Male; Neoplasm Proteins; Proteoglycans; ROC Curve; Turkey; Vasodilation; Young Adult | 2017 |
Increased asymmetric dimethylarginine levels in young men with familial Mediterranean fever (FMF): is it early evidence of interaction between inflammation and endothelial dysfunction in FMF?
Topics: Adult; Arginine; C-Reactive Protein; Case-Control Studies; Colchicine; Endothelium, Vascular; Familial Mediterranean Fever; Humans; Inflammation; Lipids; Male; Young Adult | 2008 |
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases.
Topics: Adult; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Arginine; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Glatiramer Acetate; Glutamine; HLA-D Antigens; Humans; Immunosuppressive Agents; Male; Middle Aged; Mitoxantrone; Multiple Sclerosis; Mutation; Natalizumab; Penetrance; Peptides; Phenotype; Receptors, Tumor Necrosis Factor, Type I; Sequence Analysis, DNA; Young Adult | 2008 |
Arg753Gln TLR-2 polymorphism in familial mediterranean fever: linking the environment to the phenotype in a monogenic inflammatory disease.
Topics: Amyloidosis; Arginine; Environment; Familial Mediterranean Fever; Genetic Predisposition to Disease; Glutamine; Humans; Phenotype; Point Mutation; Polymorphism, Restriction Fragment Length; Toll-Like Receptor 2 | 2006 |
Tumor necrosis factor receptor-associated periodic syndrome with a C30R mutation in a Japanese family.
Topics: Adult; Arginine; Autoimmune Diseases; Child, Preschool; Cysteine; Familial Mediterranean Fever; Female; Humans; Infant; Inflammation; Japan; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymorphism, Single Nucleotide; Receptors, Tumor Necrosis Factor, Type I | 2007 |
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.
Topics: Adult; Arginine; Diagnosis, Differential; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Heterozygote; Humans; Hypergammaglobulinemia; Male; Middle Aged; Multiple Sclerosis; Mutation; Pedigree; Prospective Studies; Receptors, Tumor Necrosis Factor, Type I | 2007 |