methionine has been researched along with Peripheral Nervous System Diseases in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 6 (40.00) | 18.7374 |
1990's | 4 (26.67) | 18.2507 |
2000's | 2 (13.33) | 29.6817 |
2010's | 2 (13.33) | 24.3611 |
2020's | 1 (6.67) | 2.80 |
Authors | Studies |
---|---|
Abed, S; Azoulay, D; Bashkin, A; Kaykov, E; Nodelman, M; Sfadi, A; Shaoul, E; Shehadeh, M; Sheleg, O | 1 |
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC | 1 |
Carter, GT; Cullen, CE; Grant, PA; Saperstein, DS; Weiss, MD | 1 |
Conceição, I; De Carvalho, M | 1 |
Ning, G; Zhang, YF | 1 |
Láhoda, F | 1 |
Golding, JP; Tonge, DA | 1 |
Alves, IL; Blake, CC; Costa, PP; Damas, AM; Matias, PM; Oliveira, P; Sakaki, Y; Saraiva, MJ; Terry, CJ | 1 |
Di Rocco, A; Werner, P | 1 |
Cohen, A; Dede, H; Erken, E; Milunsky, A; Skare, J; Skinner, M; Yazici, H | 1 |
Brimijoin, S; Nagata, H | 1 |
Alves, IL; Costa, PP; Saraiva, MJ | 1 |
Benson, MD; Dwulet, FE | 1 |
Goodman, DS; Saraiva, MJ; Sherman, W | 1 |
Krishnaswamy, K | 1 |
2 review(s) available for methionine and Peripheral Nervous System Diseases
Article | Year |
---|---|
Hypohomocysteinemia: a potentially treatable cause of peripheral neuropathology?
Topics: Aged; Female; Homocysteine; Humans; Metabolic Networks and Pathways; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Peripheral Nervous System Diseases | 2012 |
Mecobalamin.
Topics: Aged; Alprostadil; Animals; Cobamides; Coenzymes; Diabetic Neuropathies; Drug Administration Routes; Drug Therapy, Combination; Female; Folic Acid; Humans; Hyperhomocysteinemia; Hypoglycemic Agents; Kidney Failure, Chronic; Male; Metformin; Methionine; Methyltransferases; Peripheral Nervous System Diseases; Randomized Controlled Trials as Topic; Renal Dialysis; Vitamin B 12; Vitamin B 12 Deficiency; Vitamin B 6 | 2008 |
13 other study(ies) available for methionine and Peripheral Nervous System Diseases
Article | Year |
---|---|
Low brain-derived neurotrophic factor protein levels and single-nucleotide polymorphism Val66Met are associated with peripheral neuropathy in type II diabetic patients.
Topics: Adult; Aged; Amino Acid Substitution; Biomarkers; Brain-Derived Neurotrophic Factor; Case-Control Studies; Diabetes Mellitus, Type 2; Diabetic Neuropathies; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Peripheral Nervous System Diseases; Polymorphism, Single Nucleotide; Valine | 2020 |
Precancerous and non-cancer disease endpoints of chronic arsenic exposure: the level of chromosomal damage and XRCC3 T241M polymorphism.
Topics: Adult; Alleles; Amino Acid Substitution; Arsenic; Carcinogens; Case-Control Studies; Chromosome Aberrations; Conjunctivitis; DNA-Binding Proteins; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; India; Male; Methionine; Mutagens; Odds Ratio; Peripheral Nervous System Diseases; Polymorphism, Genetic; Precancerous Conditions; Skin Diseases; Threonine; Water Pollutants, Chemical | 2011 |
Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.
Topics: Adult; Age of Onset; Amino Acid Sequence; Amino Acid Substitution; Amyloid Neuropathies, Familial; Autonomic Nervous System Diseases; Female; Genetic Predisposition to Disease; Geography; Humans; Inheritance Patterns; Longitudinal Studies; Male; Methionine; Middle Aged; Mutation; Neuralgia; Peripheral Nervous System Diseases; Portugal; Prospective Studies; Sex Distribution; Valine | 2007 |
[Therapeutic possibilities in polyneuropathies].
Topics: Adult; Aged; Diabetic Neuropathies; Humans; Methionine; Middle Aged; Nervous System Diseases; Neuritis; Peripheral Nervous System Diseases; Physical Therapy Modalities; Polyneuropathies; Thioctic Acid; Transketolase; Vitamin B 12 | 1982 |
Protein synthesis and release by normal and lesioned axolotl peripheral nerves.
Topics: Ambystoma mexicanum; Animals; Autoradiography; Culture Techniques; Electrophoresis, Gel, Two-Dimensional; Heparin; Immunologic Techniques; Methionine; Nerve Tissue Proteins; Peripheral Nervous System Diseases; Reference Values; Sciatic Nerve | 1995 |
Structure of Met30 variant of transthyretin and its amyloidogenic implications.
Topics: Amino Acids; Amyloidosis; Computer Simulation; Disulfides; Methionine; Models, Molecular; Peripheral Nervous System Diseases; Prealbumin; Protein Conformation; X-Ray Diffraction | 1993 |
Hypothesis on the pathogenesis of vacuolar myelopathy, dementia, and peripheral neuropathy in AIDS.
Topics: Acquired Immunodeficiency Syndrome; AIDS Dementia Complex; Dietary Supplements; Humans; Methionine; Methylation; Peripheral Nervous System Diseases | 1999 |
Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy.
Topics: Amyloidosis; Base Sequence; DNA; Exons; Female; Homozygote; Humans; Male; Methionine; Molecular Sequence Data; Mutation; Pedigree; Peripheral Nervous System Diseases; Polymerase Chain Reaction; Prealbumin; Turkey | 1990 |
Neurotoxicity of halogenated phenylacetylureas is linked to abnormal onset of rapid axonal transport.
Topics: Animals; Axonal Transport; Gait; Male; Methionine; Motor Activity; Peripheral Nervous System Diseases; Rats; Sciatic Nerve; Sulfur Radioisotopes; Urea | 1986 |
Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
Topics: Amyloidosis; Electrophoresis, Polyacrylamide Gel; Humans; Hydrolysis; Methionine; Mutation; Peripheral Nervous System Diseases; Prealbumin; Risk Factors | 1989 |
Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I.
Topics: Adult; Amyloidosis; Cyanogen Bromide; Genetic Carrier Screening; Genetic Variation; Humans; Male; Methionine; Pedigree; Peptides; Peripheral Nervous System Diseases; Prealbumin; Sweden | 1985 |
Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin.
Topics: Amino Acid Sequence; Amyloidosis; Genetic Variation; Greece; Humans; Methionine; Pedigree; Peripheral Nervous System Diseases; Prealbumin; Valine | 1986 |
Methionine metabolism in pyridoxine deficiency.
Topics: Adult; Aspartate Aminotransferases; Cystathionine; Cysteine; Erythrocytes; Humans; Lyases; Male; Methionine; Middle Aged; Nutritional Physiological Phenomena; Peripheral Nervous System Diseases; Pyridoxine; Reflex; Sulfinic Acids; Vitamin B 6 Deficiency | 1974 |