glutamine has been researched along with Benign Paroxysmal Peritonitis in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pöllmann, W; Rübsamen, H | 1 |
| Abeliovich, D; Ben-Chetrit, E; Domingo, C; Lerer, I; Malamud, E | 1 |
4 other study(ies) available for glutamine and Benign Paroxysmal Peritonitis
| Article | Year |
|---|---|
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 |
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 |
The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant?
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Child; Cytoskeletal Proteins; Familial Mediterranean Fever; Female; Genetic Variation; Glutamic Acid; Glutamine; Humans; Jews; Male; Middle Aged; Morocco; Mutation; Pedigree; Proteins; Pyrin | 2000 |