Page last updated: 2024-08-17

methionine and BCKD Deficiency

methionine has been researched along with BCKD Deficiency in 27 studies

Research

Studies (27)

Timeframe	Studies, this research(%)	All Research%
pre-1990	25 (92.59)	18.7374
1990's	1 (3.70)	18.2507
2000's	1 (3.70)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barschak, AG; Busanello, EN; Cipriani, F; Coelho, DM; Deon, M; Dutra-Filho, CS; Giugliani, R; Sitta, A; Vargas, CR; Wajner, M	1
HOLT, LE; NORTON, PM; ROITMAN, E; SNYDERMAN, SE	2
Snyderman, SE	1
Efron, ML	1
Milner, RD; Wirdnam, PK	1
Enzenauer, J; Matz, D; Menne, F	1
Centerwall, WR; Chinnock, RF; Goodman, SI; Mace, JW	1
Guthrie, R; Jinks, DC; Vollmer, DW	1
Funayama, CA; Moura-Ribeiro, MV	1
Donnell, GN; Koch, R; Lieberman, E; Shaw, KN	1
Royer, P	1
Perrone, L	1
Levy, HL	1
Tomaszewski, L	1
Machill, G	1
Ampola, MG; Efron, ML	1
Menne, F	1
Carson, NA	1
Boisse, J	1
Rey, F; Rey, J; Sivy, M	1
Barkin, E; Levy, HL	1
van der Horst, JL; Wadman, SK	1
Fenichel, GM	1
Carpenter, DG; Carter, CH	1
Hagge, W; Irtel von Brenndorff, A	1

Reviews

4 review(s) available for methionine and BCKD Deficiency

Article	Year
Neonatal screening for inborn errors of amino acid metabolism. Clinics in endocrinology and metabolism, 1974, Volume: 3, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Biological Assay; Chromatography, Paper; Evaluation Studies as Topic; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Mass Screening; Methionine; Methods; Phenylalanine; Phenylketonurias; Pregnancy; Tyrosine	1974
The aminoacidurias. Pediatric clinics of North America, 1967, Volume: 14, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine	1967
[Feeble mindedness caused by genetic disorders of amino acid metabolism]. Hippokrates, 1968, May-31, Volume: 39, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine	1968
[New etiologic approach to periodic ketoacidosis in children]. Canadian Medical Association journal, 1971, Aug-07, Volume: 105, Issue:3 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Dehydration; Diabetic Ketoacidosis; Female; Glycogen Storage Disease; Hexoses; Humans; Hydrogen-Ion Concentration; Hypoglycemia; Infant; Infant, Newborn; Ketone Bodies; Lactation Disorders; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Methionine; Periodicity; Pregnancy; Propionates; Pyruvates; Vomiting	1971

Other Studies

23 other study(ies) available for methionine and BCKD Deficiency

Article	Year
Amino acids levels and lipid peroxidation in maple syrup urine disease patients. Clinical biochemistry, 2009, Volume: 42, Issue:6 Topics: Adult; Amino Acids; Antioxidants; Humans; Hydroxy Acids; Isoleucine; Keto Acids; Leucine; Lipid Peroxidation; Maple Syrup Urine Disease; Methionine; Oxidative Stress; Thiobarbituric Acid Reactive Substances; Tryptophan; Valine	2009
MAPLE SYRUP URINE DISEASE, WITH PARTICULAR REFERENCE TO DIETOTHERAPY. Pediatrics, 1964, Volume: 34 Topics: Amino Acid Metabolism, Inborn Errors; Anthropometry; Blood Proteins; Cerebrospinal Fluid Proteins; Diet; Diet Therapy; Erythrocytes; Exchange Transfusion, Whole Blood; Growth; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Valine	1964
A new finding in maple-syrup-urine disease. Lancet (London, England), 1962, Jan-06, Volume: 1, Issue:7219 Topics: Acer; Child; Humans; Infant; Intellectual Disability; Leucine; Maple Syrup Urine Disease; Metabolic Diseases; Methionine	1962
The therapy of maple syrup urine disease. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Child; Child, Preschool; Diet Therapy; Female; Growth; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Male; Maple Syrup Urine Disease; Methionine; Neurologic Manifestations; Valine	1967
Diet therapy for inborn errors of amino acid metabolism. Journal of the American Dietetic Association, 1967, Volume: 51, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child, Preschool; Coenzymes; Cystinuria; Diet Therapy; Hartnup Disease; Humans; Infant; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Tyrosine	1967
The pancreatic beta cell fraction in children with errors of amino acid metabolism. Pediatric research, 1982, Volume: 16, Issue:3 Topics: Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Homocystinuria; Humans; Infant; Infant, Newborn; Islets of Langerhans; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Tyrosine	1982
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2]. Medizinische Klinik, 1976, Apr-30, Volume: 71, Issue:18 Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases	1976
The child with an unusual odor. A clinical resumé. Clinical pediatrics, 1976, Volume: 15, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Choline; Diabetes Mellitus, Type 1; Diabetic Ketoacidosis; Humans; Infant; Leucine; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methionine; Odorants; Phenylketonurias; Tyrosine	1976
American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism. Pediatrics, 1976, Volume: 57, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cysteine; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Nutritional Requirements; Phenylalanine; Phenylketonurias; Risk; Tyrosine; Valine	1976
Isocratic reverse-phase liquid chromatography assay for amino acid metabolic disorders using eluates of dried blood spots. Analytical biochemistry, 1990, Aug-15, Volume: 189, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Calibration; Chromatography, Liquid; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Reference Values	1990
[Leucinosis: study of a case]. Arquivos de neuro-psiquiatria, 1985, Volume: 43, Issue:4 Topics: Female; Humans; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Valine	1985
Cystathioninuria. American journal of diseases of children (1960), 1967, Volume: 113, Issue:1 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carcinoma, Hepatocellular; Child, Preschool; Cysteine; Diet Therapy; Female; Galactosemias; Glycogen; Humans; Infant; Intellectual Disability; Liver Neoplasms; Male; Maple Syrup Urine Disease; Methionine; Middle Aged; Neuroblastoma; Phenylketonurias; Portal Vein; Pyridoxine; Serine; Sulfisoxazole; Tyrosine	1967
[Dietetics in hereditary enzyme deficiencies]. La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1970, Feb-26, Volume: 46, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970
[Diet therapy of some inborn errors of metabolism]. La Pediatria, 1974, Sep-30, Volume: 82, Issue:2 Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Celiac Disease; Child; Child, Preschool; Histidine; Humans; Hypoglycemia; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Lactose Intolerance; Leucine; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Methionine; Phenylketonurias; Proteins; Tyrosine	1974
[The inborn errors of metabolism of amino acids]. Postepy biochemii, 1973, Volume: 19, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Chemical Phenomena; Chemistry; Cystinuria; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Sarcosine; Tyrosine; Valine	1973
[Results of screening studies for phenylketonuria, maple syrup disease and homocystinuria using Guthrie's test]. Kinderarztliche Praxis, 1973, Volume: 41, Issue:5 Topics: Germany, East; Homocystinuria; Humans; Infant, Newborn; Leucine; Maple Syrup Urine Disease; Mass Screening; Methionine; Methods; Phenylalanine; Phenylketonurias	1973
Chemical pathology of amino acid diseases. Acta neurologica et psychiatrica Belgica, 1968, Volume: 68, Issue:4 Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Chemical Phenomena; Chemistry; Child; Child, Preschool; Female; Homocystine; Humans; Hypoglycemia; Infant; Intellectual Disability; Leucine; Male; Maple Syrup Urine Disease; Methionine; Pyridoxine; Valine	1968
[Rapid separation of aromatic and ramified amino acids by chromatography on ion exchange columns. Application to the surveillance of leucinosis and hyperphenylalaninemia]. Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research, 1972, Volume: 17, Issue:2 Topics: Amino Acids; Chromatography, Ion Exchange; Humans; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Methods; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1972
Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders. The Journal of laboratory and clinical medicine, 1971, Volume: 78, Issue:4 Topics: Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Aspartic Acid; Biological Transport; Child; Chromatography, Ion Exchange; Cystine; Erythrocytes; Glutamates; Glutathione; Glycine; Histidine; Homocystine; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Ornithine; Phenylketonurias; Plasma; Renal Tubular Transport, Inborn Errors; Serine; Spectrophotometry; Threonine; Tyrosine	1971
A variant form of branched-chain keto aciduria. Acta paediatrica Scandinavica, 1971, Volume: 60, Issue:5 Topics: Amino Acids; Child Behavior Disorders; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Diet Therapy; Dietary Proteins; Female; Heterozygote; Humans; Infant; Intellectual Disability; Isoleucine; Keto Acids; Leucine; Male; Maple Syrup Urine Disease; Methionine; Motor Skills; Pedigree; Phenylketonurias; Tyrosine; Valine	1971
Recent clinical advances in the treatment of neurological diseases. Pediatric clinics of North America, 1970, Volume: 17, Issue:2 Topics: Brain Diseases; Child, Preschool; Chronic Disease; Cystine; Diet Therapy; Dopamine; Folic Acid; Homocystinuria; Humans; Infant; Maple Syrup Urine Disease; Methionine; Movement Disorders; Muscular Diseases; Pyridoxine; Serotonin	1970
Inborn errors of metabolism associated with unusual odors. The Journal of the Florida Medical Association, 1970, Volume: 57, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Malabsorption Syndromes; Maple Syrup Urine Disease; Methionine; Odorants; Phenylalanine; Tryptophan; Valerates	1970
[Experiences with a new amino acid analyzer for a rapid analysis]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Amino Acids; Autoanalysis; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Premature, Diseases; Isoleucine; Leucine; Maple Syrup Urine Disease; Metabolic Diseases; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970