Page last updated: 2024-08-17

methionine and Demyelinating Diseases

methionine has been researched along with Demyelinating Diseases in 17 studies

Research

Studies (17)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (23.53)	18.7374
1990's	3 (17.65)	18.2507
2000's	6 (35.29)	29.6817
2010's	4 (23.53)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kido, J; Kitajima, M; Matsumoto, S; Mitsubuchi, H; Momosaki, K; Nakamura, K; Sawada, T; Suzuki, Y; Uetani, H	1
Hara, M; Kamei, S; Momose, M; Morita, A; Ninomiya, S; Takahashi, T; Teramoto, H	1
Aubourg, P; Bao, X; Cao, G; Köhler, W; Linnebank, M; Semmler, A; Weller, M	1
Aki, T; Asano, Y; Ito, T; Iwama, T; Miwa, K; Shinoda, J; Takenaka, S; Yokoyama, K	1
Furujo, M; Kinoshita, M; Kubo, T; Nagao, M	1
Adachi, A; Adachi, Y; Kurihara, S; Nakashima, K; Ohama, E; Wada, K	1
Csornai, M; Esik, O; Lengyel, Z; Lesznyák, J; Majtényi, K; Pisch, J; Rékó, G; Trón, L	1
Adineh, M; Bidwell, K; Dunigan, K; Ezzeddine, B; Mantil, J; Mukherjee, J; Padma, MV; Pugar, K; Satter, M; Shi, B	1
Farmand, S; Fliessbach, K; Kleczar, N; Klockgether, T; Linnebank, M; Orlopp, K; Pels, H; Schlegel, U; Schmidt-Wolf, IG; Urbach, H	1
Dinn, JJ; Scott, JM; Weir, DG; Wilson, P	1
Chamberlin, ME; Chou, JY; Leonard, JV; Mudd, SH; Ubagai, T; Wilson, WG	1
Clelland, J; Hann, I; Surtees, R	1
Allen, RH; Lindenbaum, J; Stabler, SP	1
Baethmann, M; Blom, H; Göhlich-Ratmann, G; Hoffmann, GF; Kleinlein, B; Seiffert, P; Voit, T; Wendel, U	1
Arieff, AI; Fraser, CL	1
Baldwin, GS; Carnegie, PR	1
Koenig, H	1

Reviews

3 review(s) available for methionine and Demyelinating Diseases

Article	Year
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
Relevance of vitamins, homocysteine and other metabolites in neuropsychiatric disorders. European journal of pediatrics, 1998, Volume: 157 Suppl 2 Topics: Central Nervous System Diseases; Citrates; Demyelinating Diseases; Folic Acid; Homocysteine; Humans; Mental Disorders; Methionine; Methylmalonic Acid; Vitamin B 12	1998
Hepatic encephalopathy. The New England journal of medicine, 1985, Oct-03, Volume: 313, Issue:14 Topics: Ammonia; Animals; Blood-Brain Barrier; Brain; Demyelinating Diseases; Fatty Acids; Glutamine; Hepatic Encephalopathy; Humans; Hypernatremia; Hyponatremia; Ketoglutaric Acids; Lactulose; Methionine; Neomycin; Pons; Synaptic Transmission; Tryptophan	1985

Trials

1 trial(s) available for methionine and Demyelinating Diseases

Article	Year
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

Article

Year

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

13 other study(ies) available for methionine and Demyelinating Diseases

Article	Year
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
Tumefactive Demyelinating Lesion Differentiated from a Brain Tumor Using a Combination of Magnetic Resonance Imaging and (11)C-methionine Positron Emission Tomography. Internal medicine (Tokyo, Japan), 2015, Volume: 54, Issue:11 Topics: Adrenal Cortex Hormones; Adult; Brain Neoplasms; Carbon Radioisotopes; Demyelinating Diseases; Diagnosis, Differential; Female; Humans; Magnetic Resonance Imaging; Methionine; Multiple Sclerosis; Positron-Emission Tomography; Radiography	2015
Genetic variants of methionine metabolism and X-ALD phenotype generation: results of a new study sample. Journal of neurology, 2009, Volume: 256, Issue:8 Topics: Adrenoleukodystrophy; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Cerebral Cortex; Demyelinating Diseases; DNA Mutational Analysis; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Humans; Metabolic Diseases; Methionine; Peroxisomes; Phenotype; Polymorphism, Genetic	2009
Metabolic assessment of monofocal acute inflammatory demyelination using MR spectroscopy and (11)C-methionine-, (11)C-choline-, and (18)F-fluorodeoxyglucose-PET. Brain tumor pathology, 2011, Volume: 28, Issue:3 Topics: Brain Neoplasms; Carbon Radioisotopes; Choline; Creatine; Demyelinating Diseases; Diagnosis, Differential; Female; Fluorodeoxyglucose F18; Glioma; Humans; Inflammation; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Methionine; Middle Aged; Neuroimaging; Positron-Emission Tomography	2011
Axonal and demyelinating forms of the MPZ Thr124Met mutation. Acta neurologica Scandinavica, 2003, Volume: 108, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Autopsy; Axons; Charcot-Marie-Tooth Disease; Consanguinity; Demyelinating Diseases; DNA Mutational Analysis; Female; Humans; Japan; Male; Methionine; Middle Aged; Mutation; Myelin P0 Protein; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Threonine	2003
Autopsy verifies demyelination and lack of vascular damage in partially reversible radiation myelopathy. Spinal cord, 2003, Volume: 41, Issue:10 Topics: Adult; Autopsy; Blood Vessels; Cervical Vertebrae; Demyelinating Diseases; Fatal Outcome; Female; Fluorodeoxyglucose F18; Humans; Medulla Oblongata; Meningitis; Methionine; Nerve Degeneration; Neurons; Oxygen Radioisotopes; Paraplegia; Radiation Injuries; Radiography; Radiotherapy; Spinal Cord; Spinal Cord Diseases; Thyroid Neoplasms; Tomography, Emission-Computed	2003
Functional imaging of a large demyelinating lesion. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2005, Volume: 12, Issue:2 Topics: Adult; Brain; Brain Neoplasms; Demyelinating Diseases; Diagnosis, Differential; Female; Fluorodeoxyglucose F18; Humans; Magnetic Resonance Spectroscopy; Methionine; Multiple Sclerosis; Positron-Emission Tomography; Radiography	2005
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
Pathogenesis of subacute combined degeneration: a result of methyl group deficiency. Lancet (London, England), 1981, Aug-15, Volume: 2, Issue:8242 Topics: Animals; Demyelinating Diseases; Disease Models, Animal; Humans; Macaca fascicularis; Methionine; Nitrous Oxide; Spinal Cord; Spinal Cord Diseases; Tetrahydrofolates; Vitamin B 12	1981
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency. The Journal of clinical investigation, 1996, Aug-15, Volume: 98, Issue:4 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Brain Diseases; Child; Child, Preschool; Chromosomes, Human, Pair 10; Demyelinating Diseases; Female; Genes; Humans; Infant; Male; Methionine; Methionine Adenosyltransferase; Point Mutation; Polymorphism, Single-Stranded Conformational	1996
Hydrocephalus internus in two patients with 5,10-methylenetetrahydrofolate reductase deficiency. Neuropediatrics, 2000, Volume: 31, Issue:6 Topics: 5,10-Methylenetetrahydrofolate Reductase (FADH2); Cerebral Ventricles; Demyelinating Diseases; Female; Homocysteine; Humans; Hydrocephalus; Hyperhomocysteinemia; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases	2000
Specific enzymic methylation of an arginine in the experimental allergic encephalomyelitis protein from human myelin. Science (New York, N.Y.), 1971, Feb-12, Volume: 171, Issue:3971 Topics: Amino Acid Sequence; Animals; Arginine; Autoradiography; Brain; Carbon Isotopes; Demyelinating Diseases; Encephalomyelitis, Autoimmune, Experimental; Guinea Pigs; Humans; Methionine; Methylation; Myelin Sheath; Nerve Tissue Proteins; Nucleosides; Pepsin A; Peptides; Transferases; Trypsin; Vitamin B 12 Deficiency	1971
Some observations on the experimental production of acute neuroaxonal and synaptosomal dystrophy. Acta neuropathologica, 1971, Volume: 5 Topics: Animals; Axons; Brain; Cats; Citrates; Citric Acid Cycle; Cyanides; Demyelinating Diseases; Fluorine; Fluoroacetates; Fluorouracil; Methionine; Microscopy, Electron; Mitochondrial Swelling; Oxidative Phosphorylation; Pyridines; Spinal Cord; Strychnine; Synapses	1971