Compounds > histidine
Page last updated: 2024-08-17

histidine and MS (Multiple Sclerosis)

histidine has been researched along with MS (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 MS (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