Compounds > valine

valine and Lymphohistiocytosis, Hemophagocytic

valine has been researched along with Lymphohistiocytosis, Hemophagocytic in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Barilaro, A; Brugnolo, F; Palterer, B; Parronchi, P; Sieni, E1
Aricò, M; Busiello, R; Fimiani, G; Miano, MG; Pignata, C; Santoro, A; Ursini, MV1
Biroschak, J; Bleesing, JJ; Filipovich, AH; Johnson, JA; Lee, SM; Risma, KA; Villanueva, J; Wenstrup, RJ; Zhang, K1

Other Studies

3 other study(ies) available for valine and Lymphohistiocytosis, Hemophagocytic

ArticleYear
Neuromyelitis optica, atypical hemophagocytic lymphohistiocytosis and heterozygous perforin A91V mutation.
    Journal of neuroimmunology, 2017, 10-15, Volume: 311

    Topics: Adrenal Cortex Hormones; Alanine; Antigens, CD; Humans; Lymphocytes; Lymphohistiocytosis, Hemophagocytic; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neuromyelitis Optica; Perforin; Spinal Cord; Valine

2017
A91V perforin variation in healthy subjects and FHLH patients.
    International journal of immunogenetics, 2006, Volume: 33, Issue:2

    Topics: Alanine; Amino Acid Substitution; Gene Frequency; Genetic Carrier Screening; Genetic Predisposition to Disease; Humans; Lymphohistiocytosis, Hemophagocytic; Membrane Glycoproteins; Perforin; Pore Forming Cytotoxic Proteins; Valine

2006
Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
    International journal of immunogenetics, 2007, Volume: 34, Issue:4

    Topics: Alanine; Amino Acid Substitution; Family Health; Genetic Carrier Screening; Genotype; Humans; Lymphohistiocytosis, Hemophagocytic; Membrane Glycoproteins; Mutation, Missense; Perforin; Pore Forming Cytotoxic Proteins; Valine

2007