methionine has been researched along with Aminoaciduria, Renal in 16 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 13 (81.25) | 18.7374 |
1990's | 1 (6.25) | 18.2507 |
2000's | 1 (6.25) | 29.6817 |
2010's | 1 (6.25) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Akahoshi, N; Hishiki, T; Ishii, I; Ishizaki, Y; Kamata, S; Kasahara, T; Kubota, M; Matsuura, T; Nagahata, Y; Suematsu, M; Yamada, H; Yamazaki, C; Yoshida, Y | 1 |
CHILDS, B; NYHAN, WL | 1 |
GERRITSEN, T; WAISMAN, HA | 2 |
GROSS, JB; JONES, JD; MAHER, FT; ULRICH, JA | 1 |
FINKELSTEIN, JD; IRREVERRE, F; LASTER, L; MUDD, SH | 1 |
EFRON, ML | 1 |
Eapen, CE; Jana, AK; Karnik, D; Oommen, A; Thomas, N | 1 |
Takita, H | 1 |
Efron, ML; MacCready, RA; McPherson, TC; Shih, VE; Welsh, CF | 1 |
Bartsocas, CS; Crawford, JD | 1 |
Brown, DA; Turner, B; Wilcken, B | 1 |
Cohen, PA; Gaull, GE; Sturman, JA | 1 |
Jones, JD; Ulrich, JA; Winkelmann, RK | 1 |
Scriver, CR; Whelan, DT | 1 |
Ersser, RS; Harries, JT; Lloyd, JK; Seakins, JW | 1 |
2 review(s) available for methionine and Aminoaciduria, Renal
Article | Year |
---|---|
AMINOACIDURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Biological Transport; Cystinuria; Histidine; Homocysteine; Humans; Hydroxyproline; Kidney; Methionine; Proline; Renal Aminoacidurias | 1965 |
[Renal tubule transport defect of amino acids].
Topics: Cystinuria; Hartnup Disease; Humans; Imino Acids; Kidney Tubules; Methionine; Renal Aminoacidurias | 1997 |
14 other study(ies) available for methionine and Aminoaciduria, Renal
Article | Year |
---|---|
Neutral aminoaciduria in cystathionine β-synthase-deficient mice; an animal model of homocystinuria.
Topics: Amino Acids, Neutral; Animals; Comorbidity; Cystathionine; Cystathionine beta-Synthase; Cystathionine gamma-Lyase; Disease Models, Animal; Female; Homocystinuria; Hyperhomocysteinemia; Kidney Tubules, Proximal; Male; Methionine; Mice; Mice, Inbred C57BL; Mice, Knockout; Renal Aminoacidurias | 2014 |
FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA.
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Blood; Child; Diet; Diet Therapy; Glycine; Humans; Infections; Isoleucine; Leucine; Leukocyte Count; Methionine; Renal Aminoacidurias; Threonine; Toxicology; Valine | 1964 |
HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Biochemical Phenomena; Biochemistry; Child; Homocystinuria; Humans; Infant; Intellectual Disability; Kidney; Metabolic Diseases; Methionine; Pathology; Proteins; Renal Aminoacidurias; Urologic Diseases | 1964 |
HOMOCYSTINURIA: ABSENCE OF CYSTATHIONINE IN THE BRAIN.
Topics: Amino Acids; Brain; Child; Chromatography; Cystathionine; Cystathionine beta-Synthase; Cystine; Homocystinuria; Humans; Hydro-Lyases; Kidney; Liver; Metabolic Diseases; Methionine; Nerve Tissue Proteins; Renal Aminoacidurias; Serine; Taurine; Transferases | 1964 |
ENDOGENOUS RENAL CLEARANCES OF 12 INDIVIDUAL AMINO ACIDS IN FOUR APPARENTLY HEALTHY SUBJECTS AND IN FOUR AMINOACIDURIC PERSONS OF A KINDRED WITH HEREDITARY PANCREATITIS.
Topics: Amino Acids; Arginine; Biomedical Research; Cystine; Genetics, Medical; Glutamates; Healthy Volunteers; Histidine; Isoleucine; Kidney; Leucine; Lysine; Methionine; Pancreatitis; Pancreatitis, Chronic; Phenylalanine; Physiology; Renal Aminoacidurias; Threonine; Tryptophan; Tyrosine; Valine | 1964 |
HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE.
Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine beta-Synthase; Deficiency Diseases; Genetics, Medical; Homocystinuria; Humans; Hydro-Lyases; Kidney; Liver; Liver Diseases; Methionine; Pathology; Renal Aminoacidurias; Transferases | 1964 |
Tyrosinemia type I: a clinico-laboratory case report.
Topics: alpha-Fetoproteins; Female; Humans; Infant, Newborn; Methionine; Renal Aminoacidurias; Tyrosine; Tyrosinemias | 2004 |
D-methioninuria due to DL-methionine ingestion. An artefact detected by a mass screening program for errors of amino acid metabolism.
Topics: Chromatography, Paper; Dietary Proteins; Humans; Infant, Newborn; Male; Mass Screening; Methionine; Niacinamide; Renal Aminoacidurias | 1969 |
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 |
Detection of abnormal sulphur-containing amino acid excretion in a mass urine-screening programme.
Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine; Female; Homocystinuria; Humans; Infant; Male; Mass Screening; Methionine; Renal Aminoacidurias; Sulfur | 1972 |
Metabolism of L- 35 S-methionine in vitamin B 6 deficiency: observations on cystathioninuria.
Topics: Animals; Brain; Cystathionine; Cystine; Kidney; Kinetics; Liver; Male; Methionine; Nerve Tissue Proteins; Pancreas; Proteins; Rats; Rats, Inbred Strains; Renal Aminoacidurias; Sulfur; Sulfur Isotopes; Taurine; Vitamin B 6 Deficiency | 1970 |
Urinary amino acid excretion in patients with scleroderma.
Topics: Arginine; Aspartic Acid; Chelating Agents; Female; Glutamates; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Methionine; Phenylalanine; Renal Aminoacidurias; Scleroderma, Systemic; Threonine; Tyrosine; Valine | 1971 |
Cystathioninuria and renal iminoglycinuria in a pedigree.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Child; Chromatography, Ion Exchange; Chromatography, Paper; Counseling; Female; Glycine; Heterozygote; Humans; Hydroxyproline; Infant; Infant, Newborn; Jaundice; Jews; Male; Metabolic Clearance Rate; Methionine; Middle Aged; Pedigree; Phenotype; Proline; Pyridoxine; Renal Aminoacidurias; Tryptophan | 1968 |
Recovery after dietary treatment of an infant with features of tyrosinosis.
Topics: Amino Acid Metabolism, Inborn Errors; Cholestasis; Diet Therapy; Female; Growth Disorders; Humans; Hypophosphatemia, Familial; Infant; Methionine; Phenylalanine; Phosphates; Renal Aminoacidurias; Rickets; Tyrosine | 1969 |