Page last updated: 2024-08-17

methionine and Benign Paroxysmal Peritonitis

methionine has been researched along with Benign Paroxysmal Peritonitis in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Annibal, A; Antebi, A; Braumann, M; Göbel, H; Kubacki, T; Laasch, V; Laboy, R; Müller, RU; Späth, MR; Steiner, JD1
Berendes, R; Berger, T; Berrang, J; Braunewell, L; Dressler, F; Dueckers, G; Föll, D; Giese, A; Haas, JP; Holzinger, D; Horneff, G; Jeske, M; Kallinich, T; Kamlah, C; Lainka, E; Lankisch, P; Lilienthal, E; Lohse, P; Neudorf, U; Niehues, T; Rietschel, C1
Chen, X; Dagan, T; Danon, Y; Fischel-Ghodsian, N; Halpern, GJ; Kastner, D; Lotan, R; Magal, N; Mimouni, A; Ogur, G; Rotter, JI; Schlezinger, M; Schwabe, A; Shohat, M; Shohat, T; Sirin, A1

Other Studies

3 other study(ies) available for methionine and Benign Paroxysmal Peritonitis

ArticleYear
A novel TNFRSF1A mutation associated with TNF-receptor-associated periodic syndrome and its metabolic signature.
    Rheumatology (Oxford, England), 2023, 10-03, Volume: 62, Issue:10

    Topics: Amyloidosis; Arginine; Cysteine; Familial Mediterranean Fever; Humans; Methionine; Mutation; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Tryptophan

2023
Genotype-phenotype and genotype-origin correlations in children with mediterranean fever in Germany - an AID-net study.
    Klinische Padiatrie, 2013, Volume: 225, Issue:6

    Topics: Adolescent; Alleles; Amino Acid Substitution; C-Reactive Protein; Child; Child, Preschool; Cohort Studies; Cytoskeletal Proteins; DNA Mutational Analysis; Familial Mediterranean Fever; Female; Gene Frequency; Genotype; Germany; Homozygote; Humans; Infant; Lebanon; Male; Methionine; Phenotype; Pyrin; Registries; Turkey; Valine

2013
Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis.
    European journal of human genetics : EJHG, 1999, Volume: 7, Issue:3

    Topics: Adolescent; Amyloidosis; Child; Child, Preschool; Cytoskeletal Proteins; Familial Mediterranean Fever; Female; Genotype; Humans; Male; Methionine; Phenotype; Proteins; Pyrin; Valine

1999