phenylalanine and Metabolic Diseases

phenylalanine has been researched along with Metabolic Diseases in 34 studies

Research

Studies (34)

Timeframe	Studies, this research(%)	All Research%
pre-1990	25 (73.53)	18.7374
1990's	2 (5.88)	18.2507
2000's	1 (2.94)	29.6817
2010's	3 (8.82)	24.3611
2020's	3 (8.82)	2.80

Authors

Authors	Studies
An, J; Jia, X; Li, X; Liu, R; Liu, S; Mo, Y; Wei, X; Zhang, S; Zhang, Y; Zhou, L	1
Dai, L; Dong, P; Li, Y; Wang, S	1
Candeias, NR; Gois, PMP; Gonçalves, LMD; Guedes, RC; Leandro, J; Leandro, P; Lopes, RR; Paterna, R; Russo, R; Sousa, PMF; Teixeira, M; Tomé, CS; Vicente, JB	1
Gazit, E	1
Chace, DH; De Jesús, VR; Hannon, WH; Lim, TH; Mei, JV	1
Kitahara, Y; Miura, K; Yamagishi, S	1
Schreier, K	1
EHMKE, DA; KARLE, IP; O'DONNELL, MM	1
TASHIAN, RE	1
GONCERZEWICZ, M	1
CLAYTON, BE	1
ZETTERSTROEM, R	1
AVERY, ME; MENKES, JH	1
VANDERHOEVEN, T; WOOLLEY, DW	1
BERMAN, JL; BRENCHLEY, Y; HSIA, DY; JUSTICE, P	1
CERVIO, MD; DOBON, JF; PLATER, ED	1
Kajioka, T; Kitahara, Y; Miura, K; Yamagishi, S	1
Delvalle, JA; Dienel, G; Greengard, O	1
Dhondt, JL	1
Bueno Sánchez, A; Martínez Valverde, A	1
Lutz, P	1
Kolpakov, VG	1
Haufe, F; Haufe, U; Lubs, H; Machill, G	1
Bremer, HJ; Przyrembel, H	1
Shoma, N	1
Campbell, M; Easton, EJ; Martin, JK; Simpson, I	1
McKean, CM; Peterson, NA; Shah, SN	1
Grimm, U; Knapp, A; Schlenzka, K; Tischer, W	1
Yu, JS	1
Clayton, BE; Heeley, AF; Heeley, M	1
Bunting, R; Diamond, S; Hansen, S; Perry, TL; Tischler, B; Weppler, VC	1
Hagge, W; Irtel von Brenndorff, A	1
Gjessing, LR; Seip, M; Vellan, EJ	1
Noguchi, T; Tsukada, Y	1

Reviews

3 review(s) available for phenylalanine and Metabolic Diseases

Article	Year
[Genetics of metabolic diseases. Including cystic fibrosis]. Anales espanoles de pediatria, 1990, Volume: 33 Suppl 42 Topics: Child; Child, Preschool; Cystic Fibrosis; DNA Mutational Analysis; Female; Humans; Male; Metabolic Diseases; Metabolism, Inborn Errors; Mutation; Phenylalanine; Prenatal Diagnosis	1990
[Inadequacy of the monoamine oxidase system--the probable pathogenetic factor in schizophrenia (review)]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1974, Volume: 74, Issue:8 Topics: Adenosine Triphosphatases; Adrenochrome; Amines; Animals; Brain Chemistry; Dimethoxyphenylethylamine; Dopamine; Epinephrine; Ethanolamines; Humans; Hydroxydopamines; Metabolic Diseases; Methionine; Mice; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Norepinephrine; Oxidation-Reduction; Phenylalanine; Rats; Reserpine; Schizophrenia; Tryptamines; Tryptophan	1974
[Transitory disorders of amino acid metabolism. Practical viewpoints]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Ascorbic Acid; Cystathionine; Diagnosis, Differential; Histidine; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Infant, Premature, Diseases; Male; Metabolic Diseases; Methionine; Milk Proteins; Phenylalanine; Rats; Testicular Diseases; Time Factors; Tyrosine	1973

Other Studies

31 other study(ies) available for phenylalanine and Metabolic Diseases

Article	Year
Metabolic pathway analysis of hyperuricaemia patients with hyperlipidaemia based on high-throughput mass spectrometry: a case‒control study. Lipids in health and disease, 2022, Dec-31, Volume: 21, Issue:1 Topics: Alanine; Aspartic Acid; Biomarkers; Case-Control Studies; Glycine; Humans; Hyperlipidemias; Hyperuricemia; Linoleic Acid; Mass Spectrometry; Metabolic Diseases; Metabolic Networks and Pathways; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine	2022
Untargeted and Targeted Metabolomics Reveal the Active Peptide of Molecules (Basel, Switzerland), 2023, Oct-12, Volume: 28, Issue:20 Topics: Animals; Arginine; Hominidae; Hyperlipidemias; Metabolic Diseases; Metabolomics; Peptides; Phenylalanine; Rats; Sterol Regulatory Element Binding Protein 1; Tryptophan	2023
Modulation of Human Phenylalanine Hydroxylase by 3-Hydroxyquinolin-2(1H)-One Derivatives. Biomolecules, 2021, 03-19, Volume: 11, Issue:3 Topics: Catalytic Domain; Electron Spin Resonance Spectroscopy; Fluorometry; HEK293 Cells; Humans; Metabolic Diseases; Models, Molecular; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Quinolones; Surface Plasmon Resonance; Trypsin	2021
Metabolite amyloids: a new paradigm for inborn error of metabolism disorders. Journal of inherited metabolic disease, 2016, Volume: 39, Issue:4 Topics: Amyloid; Amyloidosis; Humans; Metabolic Diseases; Metabolism, Inborn Errors; Peptides; Phenylalanine; Proteins	2016
Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry. Clinica chimica acta; international journal of clinical chemistry, 2010, May-02, Volume: 411, Issue:9-10 Topics: Amino Acids; Butanols; Carnitine; Humans; Infant, Newborn; Leucine; Metabolic Diseases; Methionine; Neonatal Screening; Palmitoylcarnitine; Phenylalanine; Quality Control; Tandem Mass Spectrometry	2010
Combination therapy with nateglinide and vildagliptin improves postprandial metabolic derangements in Zucker fatty rats. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 2010, Volume: 42, Issue:10 Topics: Adamantane; Animals; Blood Glucose; Cyclohexanes; Drug Therapy, Combination; Fatty Acids; Forkhead Transcription Factors; Hypoglycemic Agents; Insulin; Insulin-Secreting Cells; Liver; Male; Metabolic Diseases; Nateglinide; Nerve Tissue Proteins; Nitriles; Organ Size; Phenylalanine; Phosphorylation; Postprandial Period; Pyrrolidines; Rats; Rats, Zucker; Triglycerides; Vildagliptin	2010
[Congenital disorders in phenylalanine metabolism disorders]. Bibliotheca paediatrica, 1958, Issue:66 Topics: Metabolic Diseases; Phenylalanine	1958
Enzyme deficiency diseases. IIa. A phenylalanine-restricted diet. Journal of the American Dietetic Association, 1958, Volume: 34, Issue:10 Topics: Diet; Humans; Metabolic Diseases; Phenylalanine; Phenylketonurias	1958
Inhibition of brain glutamic acid decarboxylase by phenylalanine, valine, and leucine derivatives: a suggestion concerning the etiology of the neurological defect in phenylketonuria and branched-chain ketonuria. Metabolism: clinical and experimental, 1961, Volume: 10 Topics: Amino Acids; Brain; Glutamate Decarboxylase; Humans; Intellectual Disability; Ketosis; Leucine; Lyases; Maple Syrup Urine Disease; Metabolic Diseases; Phenylalanine; Phenylketonurias; Valine	1961
[Studies on the enzymatic and genetic system in phenylalanine metabolism disorders]. Pediatria polska, 1962, Volume: 37 Topics: Biochemical Phenomena; Enzymes; Geniculate Bodies; Humans; Intellectual Disability; Metabolic Diseases; Phenylalanine; Phenylketonurias; Tyrosine	1962
Symposium on metabolic diseases of the eye, Biochemical remarks on amino acid metabolism. Proceedings of the Royal Society of Medicine, 1963, Volume: 56 Topics: Alkaptonuria; Amino Acids; Humans; Metabolic Diseases; Phenylalanine; Proteins; Tyrosine	1963
TYROSINOSIS. Annals of the New York Academy of Sciences, 1963, Dec-30, Volume: 111 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Child; Genetics, Medical; Glycine; Metabolic Diseases; Phenols; Phenylalanine; Phenylpyruvic Acids; Tyrosine; Urine	1963
THE METABOLISM OF PHENYLALANINE AND TYROSINE IN THE PREMATURE INFANT. Bulletin of the Johns Hopkins Hospital, 1963, Volume: 113 Topics: Bilirubin; Blood Chemical Analysis; Folic Acid; Humans; Hydrocortisone; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Premature; Metabolic Diseases; Phenylalanine; Proteins; Tyrosine	1963
SEROTONIN DEFICIENCY IN INFANCY AS ONE CAUSE OF A MENTAL DEFECT IN PHENYLKETONURIA. Science (New York, N.Y.), 1964, May-15, Volume: 144, Issue:3620 Topics: Animals; Animals, Newborn; Behavior; Catecholamines; Chlorpromazine; Genetics; Learning; Metabolic Diseases; Metabolism; Mice; Phenylalanine; Phenylketonurias; Phenylpyruvic Acids; Research; Reserpine; Serotonin; Toxicology; Tyrosine	1964
BRAIN SEROTONIN IN EXPERIMENTAL TYROSINOSIS. Nature, 1964, May-02, Volume: 202 Topics: Amino Acid Metabolism, Inborn Errors; Ascorbic Acid; Blood; Brain; Carboxy-Lyases; Guinea Pigs; Metabolic Diseases; Monoamine Oxidase; Pharmacology; Phenylalanine; Phenylketonurias; Research; Serotonin; Toxicology; Tyrosine	1964
[Hereditary disorders of the metabolism of phenylalanine, tyrosine and tryptophan]. La Semana medica, 1961, Nov-13, Volume: 119 Topics: Biochemical Phenomena; Humans; Metabolic Diseases; Phenylalanine; Tryptophan; Tyrosine	1961
Potential utility of combination therapy with nateglinide and telmisartan for metabolic derangements in Zucker Fatty rats. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 2007, Volume: 39, Issue:12 Topics: Adiponectin; Angiotensin II Type 1 Receptor Blockers; Animals; Benzimidazoles; Benzoates; Blood Glucose; Blood Pressure; Body Weight; Cyclohexanes; Drug Therapy, Combination; Glycated Hemoglobin; Hypoglycemic Agents; Insulin; Lipids; Male; Metabolic Diseases; Nateglinide; Phenylalanine; Rats; Rats, Zucker; Telmisartan	2007
Comparison of alpha-methylphenylalanine and p-chlorophenylalanine as inducers of chronic hyperphenylalaninaemia in developing rats. The Biochemical journal, 1978, Mar-15, Volume: 170, Issue:3 Topics: Animals; Brain; Fenclonine; Liver; Metabolic Diseases; Methyltyrosines; Phenylalanine; Phenylalanine Hydroxylase; Rats; Tyrosine	1978
[Measurement of dihydropteridine reductase activity in dried blood eluates: physiological and pathological implications]. Annales de biologie clinique, 1992, Volume: 50, Issue:9 Topics: Adolescent; Adult; Biopterins; Child; Child, Preschool; Clinical Enzyme Tests; Dihydropteridine Reductase; Humans; Infant; Infant, Newborn; Metabolic Diseases; Phenylalanine	1992
[Diagnostic methods for the detection of amino acid metabolism disorders]. Monatsschrift fur Kinderheilkunde, 1973, Volume: 121, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Bacillus subtilis; Blood Protein Electrophoresis; Chemistry, Clinical; Chromatography; Clinical Enzyme Tests; Colorimetry; Fluorometry; Histidine; Humans; Leucine; Mass Screening; Metabolic Diseases; Methionine; Methods; Microbial Sensitivity Tests; Organization and Administration; Phenylalanine; Phenylketonurias; Tyrosine	1973
[Immune reactions of rats with experimental induced hyperphenylalaninemia]. Acta biologica et medica Germanica, 1972, Volume: 28, Issue:3 Topics: Animals; Antibody Formation; Candida albicans; Chlorine; Freund's Adjuvant; Hypersensitivity, Delayed; Metabolic Diseases; Nitrobenzenes; Phenylalanine; Rats; Rats, Inbred Strains	1972
[Experimental hyperphenylalanaemic animals and cystathionine contents in brain tissues]. Nihon seirigaku zasshi. Journal of the Physiological Society of Japan, 1970, Volume: 32, Issue:4 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Brain; Brain Chemistry; Diet; Dipeptides; Disease Models, Animal; Haplorhini; Hydro-Lyases; L-Serine Dehydratase; Male; Metabolic Diseases; Mixed Function Oxygenases; Phenylacetates; Phenylalanine; Phenylpyruvic Acids; Rats; Swine; Tyrosine	1970
Tyrosinemia induced by a pyridoxine antagonist, desoxypyridoxine. Clinical chemistry, 1972, Volume: 18, Issue:2 Topics: Depression, Chemical; Female; In Vitro Techniques; Lactation; Liver; Liver Cirrhosis; Male; Metabolic Diseases; Metabolism; Methanol; Phenylalanine; Pregnancy; Pyridines; Pyridoxine; Tyrosine; Urine; Vitamin B 6 Deficiency	1972
Impaired myelin formation in experimental hyperphenylalaninaemia. Journal of neurochemistry, 1972, Volume: 19, Issue:2 Topics: Animals; Brain; Cerebral Cortex; Cholesterol; DNA; Metabolic Diseases; Myelin Sheath; Nerve Tissue Proteins; Phenylalanine; Phospholipids; Rats	1972
[Phenylalanine hydroxylase activity in hyperphenyl-alaninemia and classical phenylketonuria]. Acta biologica et medica Germanica, 1972, Volume: 28, Issue:3 Topics: Adolescent; Child; Child, Preschool; Female; Humans; Liver; Male; Metabolic Diseases; Mixed Function Oxygenases; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias	1972
Screening tests for metabolic diseases. The Medical journal of Australia, 1972, Jan-01, Volume: 1, Issue:1 Topics: Australia; Blood Chemical Analysis; Chromatography, Paper; Humans; Infant; Infant, Newborn; Mass Screening; Metabolic Diseases; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias	1972
An investigation of the hyperaminoaciduria in phenylketonuria associated with the feeding of certain commercial low-phenylalanine preparations. The British journal of nutrition, 1970, Volume: 24, Issue:2 Topics: Alanine; Amino Acids; Child; Child, Preschool; Diet Therapy; Female; Humans; Hydro-Lyases; Infant; Male; Metabolic Diseases; Phenylalanine; Phenylketonurias; Proteins; Stereoisomerism; Tryptophan	1970
Unrecognized maternal biochemical disease: an uncommon cause of mental retardation in children. Journal of mental deficiency research, 1970, Volume: 14, Issue:1 Topics: Child; Cystinuria; Female; Glycine; Humans; Infant, Newborn; Intellectual Disability; Lysine; Metabolic Diseases; Phenylalanine; Phenylketonurias; Pregnancy; Proline; Tyrosine	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
Hair amino acids in cystinosis, homocystinuria, Fölling's disease and tyrosinosis. Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:3 Topics: Amino Acids; Autoanalysis; Citrulline; Cystine; Cystinosis; Female; Hair; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Male; Metabolic Diseases; Methionine; Methods; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1969
[Metabolic disorders of phenylalanine and tyrosine]. Shinkei kenkyu no shimpo. Advances in neurological sciences, 1965, Volume: 9, Issue:2 Topics: Animals; Humans; Metabolic Diseases; Metabolism, Inborn Errors; Phenylalanine; Tyrosine	1965