Page last updated: 2024-08-17

methionine and Syndrome

methionine has been researched along with Syndrome in 28 studies

Research

Studies (28)

TimeframeStudies, this research(%)All Research%
pre-199014 (50.00)18.7374
1990's3 (10.71)18.2507
2000's7 (25.00)29.6817
2010's4 (14.29)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akamine, S; Fukai, R; Hara, T; Ishizaki, Y; Kimura, M; Koga, H; Matsumoto, N; Miyake, N; Ohga, S; Ohkubo, K; Saitsu, H; Sakai, Y; Sakamoto, O; Sakata, A; Sanefuji, M; Torisu, H; Yamaguchi, S1
Damgaard, RB; Elliott, PR; Komander, D; Maher, ER; Marco-Casanova, P; McHale, D; McKenzie, ANJ; Morgan, NV; Titheradge, HL; Walker, JA1
Cloutier, S; Duan, Z; Jackson, SC; Poon, MC; Rand, ML; Sinclair, GD1
Hattersley, AT; Jones, AG1
Deguchi, A; Mineo, I; Okauchi, Y; Suehara, S1
KELLAWAY, P; PROLER, M1
Barshop, BA; Haas, RH; McGowan, KA; Naviaux, RK; Nyhan, WL; Townsend, JJ; Yu, A1
ELVEHJEM, CA; HANKES, LV1
Demaerel, P; Flamen, P; Legius, E; Mortelmans, L; Plets, C; Sciot, R; Van Calenbergh, F; Vantomme, N1
Abdulsabur, N; Antshel, KM; Colgan, D; Fremont, W; Funke, B; Higgins, AM; Kates, WR; Kucherlapati, R; Shprintzen, RJ1
Bassett, AS; Caluseriu, O; Chow, EW; Weksberg, R; Young, DA1
Osborne, CA; Polzin, DJ1
Bender, AN; Gaull, GE; Schaffner, F; Tallan, HH; Vulovic, D1
Dea, S; Mardassi, H; Mounir, S1
Deprez, M; Fridman, V; Gosseye, S; Hubert, AF; Lambert, Y; Lombet, J; Rigo, J; Sokal, E; Verloes, A1
Arveiler, D; Aumont, MC; de Prost, D; Desprez, S; Dhermy, D; Evans, A; Fumeron, F; Galand, C; Garbarz, M; Hakim, J; Luc, G; Moatti, D; Ollivier, V; Poirier, O; Ruidavets, JB; Seknadji, P1
Beavis, RC; Bugiani, O; Frangione, B; Ghetti, B; Giaccone, G; Lievens, PM; Mohr, M; Perini, F; Piccardo, P; Prelli, F; Rossi, G; Salmona, M; Tagliavini, F; Tranchant, C; Warter, JM1
Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S1
Awasthi, YC; Morris, HH; Powell, GF; Schmalstieg, FC; Schochet, SS; Srivastava, SK1
Roberson, RH; Trujillo, T1
Chalmers, RA; Lawson, AM; Liberman, MM; Watts, RW1
Hashimoto, T; Schram, AW; Schutgens, RB; Strijland, A; Tager, JM; van den Bosch, H; Wanders, RJ1
Hedo, JA; Moncada, VY; Serrano-Rios, M; Taylor, SI1
Bartsocas, CS; Crawford, JD1
Gilchrist, P; Hemsley, LA; Payne, CG; Pearson, JA1
Buxton, BH; Curzon, G; Fenton, G; Kantamaneni, BD; Parkes, JD; Record, C; Struthers, G1
Murphy, D; Wolford, JH1
Bannister, DW; Blair, R; Evans, AJ; Whitehead, CC1

Reviews

1 review(s) available for methionine and Syndrome

ArticleYear
Medical prophylaxis of feline lower urinary tract disorders.
    The Veterinary clinics of North America. Small animal practice, 1984, Volume: 14, Issue:3

    Topics: Ammonium Chloride; Animal Feed; Animals; Anti-Infective Agents; Cat Diseases; Cats; Ethylenediamines; Magnesium; Methionine; Polyphosphates; Sodium Chloride; Syndrome; Urinary Calculi; Urinary Tract Infections; Urologic Diseases

1984

Other Studies

27 other study(ies) available for methionine and Syndrome

ArticleYear
A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia.
    European journal of medical genetics, 2018, Volume: 61, Issue:8

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Brain Diseases; Humans; Male; Methionine; Methylmalonic Acid; Propionates; Protein Serine-Threonine Kinases; Syndrome

2018
The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity.
    Cell, 2016, Aug-25, Volume: 166, Issue:5

    Topics: Animals; Antibodies, Neutralizing; Autoimmune Diseases; Autoimmunity; B-Lymphocytes; Cytokines; Deubiquitinating Enzymes; Disease Models, Animal; Endopeptidases; Germ-Line Mutation; Humans; Inflammation; Infliximab; Methionine; Mice; Mice, Mutant Strains; Myeloid Cells; Polyubiquitin; Sequence Deletion; Syndrome; T-Lymphocytes; Tumor Necrosis Factor-alpha

2016
The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation.
    Blood, 2009, Apr-02, Volume: 113, Issue:14

    Topics: Amino Acid Substitution; Blood Coagulation Tests; Blood Platelet Disorders; Blood Platelets; DNA Mutational Analysis; Family; Female; Humans; Male; Methionine; Mutation, Missense; Pedigree; Platelet Aggregation; Syndrome; Valine; von Willebrand Diseases; von Willebrand Factor

2009
Reevaluation of a case of type 1 diabetes mellitus diagnosed before 6 months of age.
    Nature reviews. Endocrinology, 2010, Volume: 6, Issue:6

    Topics: Administration, Oral; Adolescent; Amino Acid Substitution; Developmental Disabilities; Diabetes Mellitus, Type 1; Dose-Response Relationship, Drug; Epilepsy; Female; Glyburide; Glycated Hemoglobin; Humans; Hypoglycemic Agents; Infant; Methionine; Mutation; Potassium Channels, Inwardly Rectifying; Syndrome; Valine

2010
Insulin autoimmune syndrome in a health supplement user: the effectiveness of cornstarch therapy for treating hypoglycemia.
    Internal medicine (Tokyo, Japan), 2013, Volume: 52, Issue:3

    Topics: Aged; Autoantibodies; Autoimmune Diseases; Dietary Supplements; Female; HLA-DR4 Antigen; HLA-DRB1 Chains; Humans; Hypoglycemia; Insulin; Insulin Antibodies; Methionine; Starch; Syndrome

2013
The methionine sulfoximine syndrome in the cat.
    Epilepsia, 1962, Volume: 3

    Topics: Animals; Behavior; Cats; Epilepsy; Methionine; Methionine Sulfoximine; Syndrome

1962
The role of methionine in ethylmalonic encephalopathy with petechiae.
    Archives of neurology, 2004, Volume: 61, Issue:4

    Topics: Amino Acids; Brain; Brain Diseases, Metabolic, Inborn; Caudate Nucleus; Fatal Outcome; Female; Follow-Up Studies; Humans; Infant; Isoleucine; Male; Malonates; Methionine; Pedigree; Purpura; Substantia Nigra; Syndrome

2004
A nervous syndrome produced with phenylalanine and methionine.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1949, Volume: 72, Issue:2

    Topics: Humans; Methionine; Nervous System; Phenylalanine; Syndrome

1949
Lhermitte-Duclos disease: 11C-methionine positron emission tomography data in 4 patients.
    Surgical neurology, 2006, Volume: 65, Issue:3

    Topics: Adult; Amino Acids; Carbon Radioisotopes; Cerebellar Diseases; Cerebellar Neoplasms; Cerebellum; Dominance, Cerebral; Female; Granular Cell Tumor; Hamartoma Syndrome, Multiple; Humans; Hyperplasia; Magnetic Resonance Imaging; Male; Methionine; Positron-Emission Tomography; Purkinje Cells; Syndrome

2006
A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome).
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2006, Apr-05, Volume: 141B, Issue:3

    Topics: Abnormalities, Multiple; Adolescent; Alleles; Brain; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; DNA Mutational Analysis; Face; Female; Gene Frequency; Genotype; Heart Defects, Congenital; Humans; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Sex Factors; Syndrome; Task Performance and Analysis; Valine; Velopharyngeal Insufficiency

2006
Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.
    Biological psychiatry, 2007, May-15, Volume: 61, Issue:10

    Topics: Adult; Alleles; Amino Acid Substitution; Arousal; Chromosome Deletion; Chromosomes, Human, Pair 22; Female; Frontal Lobe; Gene Expression; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia; Syndrome; Valine

2007
Methioninemia and myopathy: a new disorder.
    Annals of neurology, 1981, Volume: 9, Issue:5

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Diagnosis, Differential; Female; Humans; Intellectual Disability; Liver; Methionine; Methionine Adenosyltransferase; Microscopy, Electron; Muscles; Muscular Diseases; Syndrome

1981
Structural gene analysis of a Quebec reference strain or porcine reproductive and respiratory syndrome virus (PRRSV).
    Advances in experimental medicine and biology, 1995, Volume: 380

    Topics: Animals; Base Sequence; Caliciviridae; Caliciviridae Infections; Consensus Sequence; Electrophoresis, Polyacrylamide Gel; Europe; Genes, Viral; Methionine; Molecular Weight; Open Reading Frames; Protein Biosynthesis; Quebec; Respiratory Tract Infections; Sulfur Radioisotopes; Swine; Swine Diseases; Syndrome; Viral Proteins; Viral Structural Proteins

1995
Tricho-hepato-enteric syndrome: further delineation of a distinct syndrome with neonatal hemochromatosis phenotype, intractable diarrhea, and hair anomalies.
    American journal of medical genetics, 1997, Feb-11, Volume: 68, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Diarrhea; Face; Female; Hair; Hemochromatosis; Humans; Infant; Infant, Newborn; Liver; Lung; Male; Methionine; Pregnancy; Syndrome

1997
Polymorphisms of the tissue factor pathway inhibitor (TFPI) gene in patients with acute coronary syndromes and in healthy subjects : impact of the V264M substitution on plasma levels of TFPI.
    Arteriosclerosis, thrombosis, and vascular biology, 1999, Volume: 19, Issue:4

    Topics: Acute Disease; Adult; Aged; Amino Acid Sequence; Amino Acid Substitution; Angina, Unstable; Case-Control Studies; Coronary Disease; France; Gene Frequency; Genotype; Humans; Lipoproteins; Male; Methionine; Middle Aged; Molecular Sequence Data; Myocardial Infarction; Polymorphism, Genetic; Risk Factors; Syndrome; Valine

1999
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
    The Journal of biological chemistry, 2001, Feb-23, Volume: 276, Issue:8

    Topics: Adult; Alleles; Amyloid; Cerebral Cortex; Gerstmann-Straussler-Scheinker Disease; Heterozygote; Humans; Male; Methionine; Peptide Fragments; Prion Proteins; Prions; Protein Precursors; Sequence Analysis, Protein; Syndrome; Valine

2001
A novel mutation, P126R, in a Japanese patient with HHH syndrome.
    Pediatric neurology, 2002, Volume: 26, Issue:1

    Topics: Adolescent; Ammonia; Base Sequence; Brain Diseases; Carrier Proteins; Cysts; DNA Primers; Exons; Gene Expression; Humans; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Methionine; Mitochondrial Diseases; Molecular Sequence Data; Ornithine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Septum Pellucidum; Syndrome; Tomography, X-Ray Computed

2002
Studies in neuronal ceroid-lipofuscinosis: leukocyte peroxidase deficiency in a patient with neuronal ceroid-lipofuscinosis (Jansky-Bielschowsky type).
    The Journal of laboratory and clinical medicine, 1977, Volume: 89, Issue:4

    Topics: Ascorbic Acid; Child, Preschool; Humans; In Vitro Techniques; Leukocytes; Lipidoses; Methionine; Peroxidases; Syndrome; Vitamin B 12; Vitamin E

1977
The effect of methionine, thiouracil, dienestrol diacetate and thyroprotein on the development and prevention of fatty liver in pullets.
    Poultry science, 1975, Volume: 54, Issue:3

    Topics: Adipose Tissue; Animal Feed; Animals; Caseins; Chickens; Dienestrol; Eggs; Fatty Liver; Female; Hematoma; Hemorrhage; Iodoproteins; Lipid Metabolism; Liver; Liver Diseases; Methionine; Phenols; Phosphorus; Poultry Diseases; Syndrome; Thiouracil

1975
Some biochemical effects of chloral hydrate in an infant with a tyrosinemia-like syndrome.
    Pediatric research, 1975, Volume: 9, Issue:12

    Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Ascorbic Acid; Chloral Hydrate; Female; Humans; Hydrocephalus; Infant; Lactates; Methionine; Oxygenases; Phenylacetates; Phenylalanine; Phenylpyruvic Acids; Syndrome; Tyrosine

1975
Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.
    Proceedings of the National Academy of Sciences of the United States of America, 1986, Volume: 83, Issue:16

    Topics: Abnormalities, Multiple; Acetyl-CoA C-Acetyltransferase; Acetyltransferases; Acyl-CoA Oxidase; Catalase; Cell Line; Diffuse Cerebral Sclerosis of Schilder; Fibroblasts; Humans; Infant; Leucine; Methionine; Microbodies; Oxidation-Reduction; Oxidoreductases; Reference Values; Refsum Disease; Syndrome

1986
Insulin-receptor biosynthesis in cultured lymphocytes from an insulin-resistant patient (Rabson-Mendenhall syndrome). Evidence for defect before insertion of receptor into plasma membrane.
    Diabetes, 1986, Volume: 35, Issue:7

    Topics: Cell Membrane; Cells, Cultured; Humans; Insulin Resistance; Lymphocytes; Mannose; Methionine; Protein Precursors; Radioligand Assay; Receptor, Insulin; Syndrome

1986
Clinical phenotypes in kidney transport disorders.
    Birth defects original article series, 1974, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Acidosis, Renal Tubular; Cerebrospinal Fluid Proteins; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria; Diabetes Insipidus; Galactose; Glucose; Glycosuria, Renal; Growth Disorders; Hartnup Disease; Humans; Hypophosphatemia, Familial; Kidney Tubules; Malabsorption Syndromes; Methionine; Phenotype; Pseudohypoparathyroidism; Pulmonary Heart Disease; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Seizures; Syndrome

1974
Involvement of biotin in the fatty liver and kidney syndrome of broilers.
    British poultry science, 1974, Volume: 15, Issue:5

    Topics: Animal Feed; Animals; Biotin; Diet; Fatty Liver; Housing, Animal; Kidney Diseases; Lysine; Methionine; Poultry Diseases; Syndrome; Triticum; Tryptophan; Vitamins

1974
Narcolepsy and cataplexy. Clinical features, treatment and cerebrospinal fluid findings.
    The Quarterly journal of medicine, 1974, Volume: 43, Issue:172

    Topics: Adult; Amphetamine; Aspartic Acid; Body Weight; Cataplexy; Cerebrospinal Fluid Proteins; Dextroamphetamine; Electroencephalography; Feeding and Eating Disorders; Female; Homovanillic Acid; Humans; Libido; Male; Mental Disorders; Methionine; Middle Aged; Narcolepsy; Phenylalanine; Syndrome; Tyrosine

1974
Effect of diet on fatty liver-hemorrhagic syndrome incidence in laying chickens.
    Poultry science, 1972, Volume: 51, Issue:6

    Topics: Animals; Body Weight; Chickens; Choline; Cobalt; Diet; Fatty Liver; Female; Hemorrhage; Inositol; Lipids; Liver; Methionine; Poultry Diseases; Selenium; Syndrome; Vitamin B 12; Vitamin E

1972
Involvement of diet in fatty liver and kidney syndrome in broiler chickens.
    The Veterinary record, 1973, Feb-03, Volume: 92, Issue:5

    Topics: Animal Feed; Animals; Chickens; Choline; Diet; Edible Grain; Fatty Liver; Kidney; Kidney Diseases; Lipid Metabolism; Liver; Methionine; Poultry Diseases; Selenium; Syndrome; Vitamin B 12

1973