Compounds > histidine
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histidine and Multiple Sclerosis

histidine has been researched along with Multiple Sclerosis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's0 (0.00)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Kačer, D; Štětkářová, I; Valeš, K; Židó, M; Zimová, D1
Cunningham, JM; Dyck, PJ; Kilfoyle, DH; Klein, CJ; Klein, DM; Kumar, N; Litchy, WJ; Wu, Y1
Garcia-Sanchez, MI; Izquierdo, G; Lucas, M; Marcos, A; Ortiz, L; Solano, F; Suarez, R; Venegas, A1
Battaloglu, E; Ciftci, F; Deymeer, F; Eraksoy, M; Halefoglu, AM; Oge, AE; Parman, Y; Poyraz, M; Saruhan-Direskeneli, G1
Mrksich, M; Patrie, SM1
Khokhlov, AP; Mel'nichuk, PV; Rogovina, NI1

Other Studies

6 other study(ies) available for histidine and Multiple Sclerosis

ArticleYear
Metabolomics of Cerebrospinal Fluid Amino and Fatty Acids in Early Stages of Multiple Sclerosis.
    International journal of molecular sciences, 2023, Nov-13, Volume: 24, Issue:22

    Topics: Biomarkers; Central Nervous System; Fatty Acids; Histidine; Humans; Metabolomics; Multiple Sclerosis

2023
Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis.
    Journal of neurology, neurosurgery, and psychiatry, 2006, Volume: 77, Issue:8

    Topics: Adult; Age of Onset; Child, Preschool; DNA Mutational Analysis; Female; Hearing Loss; Hereditary Sensory and Autonomic Neuropathies; Histidine; Humans; Male; Middle Aged; Multiple Sclerosis; Myelin P0 Protein; Pedigree; Phenotype; Proline; Restless Legs Syndrome

2006
Arg113His mutation of vanishing white matter is not present in multiple sclerosis.
    Multiple sclerosis (Houndmills, Basingstoke, England), 2007, Volume: 13, Issue:3

    Topics: Adolescent; Amino Acid Substitution; Arginine; Brain; Female; Functional Laterality; Histidine; Humans; Male; Multiple Sclerosis; Pedigree; Polymorphism, Restriction Fragment Length; Polymorphism, Single Nucleotide

2007
X-linked Charcot-Marie-Tooth disease and multiple sclerosis.
    Journal of neurology, 2007, Volume: 254, Issue:7

    Topics: Adult; Central Nervous System; Charcot-Marie-Tooth Disease; Chromosomes, Human, X; Connexins; Gap Junction beta-1 Protein; Histidine; Humans; Magnetic Resonance Imaging; Male; Multiple Sclerosis; Mutation; Tyrosine

2007
Self-assembled monolayers for MALDI-TOF mass spectrometry for immunoassays of human protein antigens.
    Analytical chemistry, 2007, Aug-01, Volume: 79, Issue:15

    Topics: Antigens; Chelating Agents; Chemistry, Clinical; Cystatin C; Cystatins; Enzymes, Immobilized; Histidine; Humans; Immunoassay; Immunoglobulin G; Multiple Sclerosis; Nerve Tissue Proteins; Nickel; Proteins; Sensitivity and Specificity; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Staphylococcal Protein A

2007
[Changes of clinico-biochemical indicators in multiple sclerosis treated with hormones and antioxidants].
    Sovetskaia meditsina, 1980, Issue:6

    Topics: Adult; Female; Histidine; Humans; Lipid Peroxides; Male; Malonates; Malondialdehyde; Middle Aged; Multiple Sclerosis; Prednisolone

1980