Page last updated: 2024-08-23

s-adenosylmethionine and Demyelinating Diseases

s-adenosylmethionine has been researched along with Demyelinating Diseases in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (42.86)18.2507
2000's2 (28.57)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kido, J; Kitajima, M; Matsumoto, S; Mitsubuchi, H; Momosaki, K; Nakamura, K; Sawada, T; Suzuki, Y; Uetani, H1
Furujo, M; Kinoshita, M; Kubo, T; Nagao, M1
Farmand, S; Fliessbach, K; Kleczar, N; Klockgether, T; Linnebank, M; Orlopp, K; Pels, H; Schlegel, U; Schmidt-Wolf, IG; Urbach, H1
Clelland, J; Hann, I; Surtees, R1
Surtees, R1
Guiloff, RJ; Tan, SV1
Chazerain, P; Moulonguet, A; Olivero de Rubiana, JP; Vinciguerra, C; Ziza, JM1

Reviews

4 review(s) available for s-adenosylmethionine and Demyelinating Diseases

ArticleYear
Methionine adenosyltransferase I/III deficiency: neurological manifestations and relevance of S-adenosylmethionine.
    Molecular genetics and metabolism, 2012, Volume: 107, Issue:3

    Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Brain; Demyelinating Diseases; Diet; Genetic Testing; Glycine N-Methyltransferase; Humans; Infant, Newborn; Isoenzymes; Methionine; Methionine Adenosyltransferase; Mutation; S-Adenosylmethionine; Severity of Illness Index

2012
Demyelination and inborn errors of the single carbon transfer pathway.
    European journal of pediatrics, 1998, Volume: 157 Suppl 2

    Topics: Demyelinating Diseases; Humans; Liver; Metabolism, Inborn Errors; Methionine Adenosyltransferase; Methylation; Myelin Basic Protein; One-Carbon Group Transferases; S-Adenosylmethionine

1998
Hypothesis on the pathogenesis of vacuolar myelopathy, dementia, and peripheral neuropathy in AIDS.
    Journal of neurology, neurosurgery, and psychiatry, 1998, Volume: 65, Issue:1

    Topics: Acquired Immunodeficiency Syndrome; AIDS Dementia Complex; Cytokines; Demyelinating Diseases; Folic Acid; Glutathione; Humans; Macrophage Activation; Oligodendroglia; Peripheral Nervous System Diseases; S-Adenosylmethionine; Spinal Cord Diseases; Vacuoles; Vitamin B 12

1998
[Postoperative combined medullary sclerosis revealing Biermer's disease: toxic effect of nitrous oxide].
    Revue neurologique, 2000, Volume: 156, Issue:6-7

    Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Abscess; Aged; Anemia, Pernicious; Anesthetics, Inhalation; Arthroplasty, Replacement, Hip; Atrophy; Autoantibodies; Autoimmune Diseases; Demyelinating Diseases; Female; Gastric Mucosa; Humans; Intestinal Absorption; Intrinsic Factor; Nitrous Oxide; Oxidation-Reduction; Paresthesia; Postoperative Complications; Proprioception; S-Adenosylmethionine; Sclerosis; Spinal Cord; Spinal Cord Diseases; Surgical Wound Infection; Vitamin B 12

2000

Trials

1 trial(s) available for s-adenosylmethionine and Demyelinating Diseases

ArticleYear
Demyelination and single-carbon transfer pathway metabolites during the treatment of acute lymphoblastic leukemia: CSF studies.
    Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 1998, Volume: 16, Issue:4

    Topics: Antidotes; Antimetabolites, Antineoplastic; Central Nervous System; Child; Child, Preschool; Combined Modality Therapy; Demyelinating Diseases; Drug Interactions; Humans; Infant; Leucovorin; Methionine; Methotrexate; Myelin Basic Protein; Precursor Cell Lymphoblastic Leukemia-Lymphoma; S-Adenosylmethionine; Tetrahydrofolates

1998

Other Studies

2 other study(ies) available for s-adenosylmethionine and Demyelinating Diseases

ArticleYear
Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract.
    Brain & development, 2019, Volume: 41, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Brain; Demyelinating Diseases; Glycine N-Methyltransferase; Humans; Infant; Infant, Newborn; Male; Methionine; Methionine Adenosyltransferase; Neonatal Screening; Nervous System Diseases; Pontine Tegmentum; S-Adenosylmethionine

2019
MTX-induced white matter changes are associated with polymorphisms of methionine metabolism.
    Neurology, 2005, Mar-08, Volume: 64, Issue:5

    Topics: Aged; Brain; Central Nervous System Neoplasms; Demyelinating Diseases; DNA Mutational Analysis; Drug Resistance; Female; Folic Acid; Folic Acid Antagonists; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Haplotypes; Humans; Lymphoma; Male; Methionine; Methotrexate; Middle Aged; Myelin Sheath; Nerve Fibers, Myelinated; Neurotoxins; Polymorphism, Genetic; Risk Factors; S-Adenosylmethionine

2005