methionine has been researched along with Syndrome in 28 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 14 (50.00) | 18.7374 |
| 1990's | 3 (10.71) | 18.2507 |
| 2000's | 7 (25.00) | 29.6817 |
| 2010's | 4 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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, S | 1 |
| Damgaard, RB; Elliott, PR; Komander, D; Maher, ER; Marco-Casanova, P; McHale, D; McKenzie, ANJ; Morgan, NV; Titheradge, HL; Walker, JA | 1 |
| Cloutier, S; Duan, Z; Jackson, SC; Poon, MC; Rand, ML; Sinclair, GD | 1 |
| Hattersley, AT; Jones, AG | 1 |
| Deguchi, A; Mineo, I; Okauchi, Y; Suehara, S | 1 |
| KELLAWAY, P; PROLER, M | 1 |
| Barshop, BA; Haas, RH; McGowan, KA; Naviaux, RK; Nyhan, WL; Townsend, JJ; Yu, A | 1 |
| ELVEHJEM, CA; HANKES, LV | 1 |
| Demaerel, P; Flamen, P; Legius, E; Mortelmans, L; Plets, C; Sciot, R; Van Calenbergh, F; Vantomme, N | 1 |
| Abdulsabur, N; Antshel, KM; Colgan, D; Fremont, W; Funke, B; Higgins, AM; Kates, WR; Kucherlapati, R; Shprintzen, RJ | 1 |
| Bassett, AS; Caluseriu, O; Chow, EW; Weksberg, R; Young, DA | 1 |
| Osborne, CA; Polzin, DJ | 1 |
| Bender, AN; Gaull, GE; Schaffner, F; Tallan, HH; Vulovic, D | 1 |
| Dea, S; Mardassi, H; Mounir, S | 1 |
| Deprez, M; Fridman, V; Gosseye, S; Hubert, AF; Lambert, Y; Lombet, J; Rigo, J; Sokal, E; Verloes, A | 1 |
| 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, P | 1 |
| 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, JM | 1 |
| Hayakawa, C; Kanazawa, N; Miyamoto, T; Tsujino, S | 1 |
| Awasthi, YC; Morris, HH; Powell, GF; Schmalstieg, FC; Schochet, SS; Srivastava, SK | 1 |
| Roberson, RH; Trujillo, T | 1 |
| Chalmers, RA; Lawson, AM; Liberman, MM; Watts, RW | 1 |
| Hashimoto, T; Schram, AW; Schutgens, RB; Strijland, A; Tager, JM; van den Bosch, H; Wanders, RJ | 1 |
| Hedo, JA; Moncada, VY; Serrano-Rios, M; Taylor, SI | 1 |
| Bartsocas, CS; Crawford, JD | 1 |
| Gilchrist, P; Hemsley, LA; Payne, CG; Pearson, JA | 1 |
| Buxton, BH; Curzon, G; Fenton, G; Kantamaneni, BD; Parkes, JD; Record, C; Struthers, G | 1 |
| Murphy, D; Wolford, JH | 1 |
| Bannister, DW; Blair, R; Evans, AJ; Whitehead, CC | 1 |
1 review(s) available for methionine and Syndrome
| Article | Year |
|---|---|
Medical prophylaxis of feline lower urinary tract disorders.
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 |
27 other study(ies) available for methionine and Syndrome
| Article | Year |
|---|---|
A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia.
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.
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.
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.
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.
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.
Topics: Animals; Behavior; Cats; Epilepsy; Methionine; Methionine Sulfoximine; Syndrome | 1962 |
The role of methionine in ethylmalonic encephalopathy with petechiae.
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.
Topics: Humans; Methionine; Nervous System; Phenylalanine; Syndrome | 1949 |
Lhermitte-Duclos disease: 11C-methionine positron emission tomography data in 4 patients.
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).
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.
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.
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).
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.
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.
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.
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.
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).
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 |