Page last updated: 2024-08-17

methionine and Peripheral Nerve Diseases

methionine has been researched along with Peripheral Nerve Diseases in 15 studies

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19906 (40.00)18.7374
1990's4 (26.67)18.2507
2000's2 (13.33)29.6817
2010's2 (13.33)24.3611
2020's1 (6.67)2.80

Authors

AuthorsStudies
Abed, S; Azoulay, D; Bashkin, A; Kaykov, E; Nodelman, M; Sfadi, A; Shaoul, E; Shehadeh, M; Sheleg, O1
Banerjee, S; Das, JK; Ghosh, P; Giri, AK; Kundu, M; Mitra, S; Sau, TJ; States, JC1
Carter, GT; Cullen, CE; Grant, PA; Saperstein, DS; Weiss, MD1
Conceição, I; De Carvalho, M1
Ning, G; Zhang, YF1
Láhoda, F1
Golding, JP; Tonge, DA1
Alves, IL; Blake, CC; Costa, PP; Damas, AM; Matias, PM; Oliveira, P; Sakaki, Y; Saraiva, MJ; Terry, CJ1
Di Rocco, A; Werner, P1
Cohen, A; Dede, H; Erken, E; Milunsky, A; Skare, J; Skinner, M; Yazici, H1
Brimijoin, S; Nagata, H1
Alves, IL; Costa, PP; Saraiva, MJ1
Benson, MD; Dwulet, FE1
Goodman, DS; Saraiva, MJ; Sherman, W1
Krishnaswamy, K1

Reviews

2 review(s) available for methionine and Peripheral Nerve Diseases

ArticleYear
Hypohomocysteinemia: a potentially treatable cause of peripheral neuropathology?
    Physical medicine and rehabilitation clinics of North America, 2012, Volume: 23, Issue:1

    Topics: Aged; Female; Homocysteine; Humans; Metabolic Networks and Pathways; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Peripheral Nervous System Diseases

2012
Mecobalamin.
    Expert opinion on investigational drugs, 2008, Volume: 17, Issue:6

    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

Other Studies

13 other study(ies) available for methionine and Peripheral Nerve Diseases

ArticleYear
Low brain-derived neurotrophic factor protein levels and single-nucleotide polymorphism Val66Met are associated with peripheral neuropathy in type II diabetic patients.
    Acta diabetologica, 2020, Volume: 57, Issue:7

    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.
    Mutation research, 2011, Jan-10, Volume: 706, Issue:1-2

    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.
    Muscle & nerve, 2007, Volume: 35, Issue:1

    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].
    Fortschritte der Medizin, 1982, Oct-14, Volume: 100, Issue:38

    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.
    Experimental neurology, 1995, Volume: 134, Issue:1

    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.
    The EMBO journal, 1993, Volume: 12, Issue:2

    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.
    Journal of neurology, neurosurgery, and psychiatry, 1999, Volume: 66, Issue:4

    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.
    Human genetics, 1990, Volume: 86, Issue:1

    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.
    Brain research, 1986, Oct-15, Volume: 385, Issue:1

    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.
    Clinical chemistry, 1989, Volume: 35, Issue:6

    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.
    The Journal of clinical investigation, 1985, Volume: 75, Issue:1

    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.
    The Journal of laboratory and clinical medicine, 1986, Volume: 108, Issue:1

    Topics: Amino Acid Sequence; Amyloidosis; Genetic Variation; Greece; Humans; Methionine; Pedigree; Peripheral Nervous System Diseases; Prealbumin; Valine

1986
Methionine metabolism in pyridoxine deficiency.
    Nutrition and metabolism, 1974, Volume: 17, Issue:1

    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