phenylalanine and Nervous System Diseases

phenylalanine has been researched along with Nervous System Diseases in 30 studies

Research

Studies (30)

TimeframeStudies, this research(%)All Research%
pre-199017 (56.67)18.7374
1990's4 (13.33)18.2507
2000's2 (6.67)29.6817
2010's6 (20.00)24.3611
2020's1 (3.33)2.80

Authors

AuthorsStudies
Charriere, S; Douillard, C; Feillet, F; Fouilhoux, A; Jaulent, P; Thobois, S1
Huijbregts, SCJ; Jahja, R; van Ginkel, WG; van Spronsen, FJ1
Dayanath, BKTP; Dayasiri, KC; Jasinge, E; Nawarathne, D; Senanayake, UE; Suraweera, N; Weerasekara, K1
Anwar, MS; O'Riordan, J; Waddell, B1
Corbo, C; Daniele, A; Imperlini, E; Orrù, S; Salvatore, F1
Choudhary, AK; Lee, YY1
Beblo, S; Demmelmair, H; Hanebutt, FL; Koletzko, B1
Bik-Multanowski, M; Mozrzymas, R; Pietrzyk, JJ1
Chang, M; He, C; Hsiao, KJ; Liu, TT; Shen, M; Shen, S; Wang, L; Yu, WM; Zhang, Z; Zhou, Z1
Leeming, RJ1
Beck, B; Brandt, NJ; Christensen, E; Niederwieser, A; Pedersen, PS1
Baba, M; Ishimaru, K; Matsunaga, M; Takebe, K; Tamasawa, N1
Azen, C; de la Cruz, F; Friedman, E; Hanley, W; Koch, R; Matalon, R; Rouse, B; Shifrin, H; Trefz, F1
Fünders, B; Güttler, F; Harms, E; Pietsch, M; Ullrich, K; Weglage, J1
Abroms, IF; Breslow, JL; Brewster, TG; Kaufman, S; Milstien, S; Moskowitz, MA1
Friedman, EG; Johnson, CF; Koch, R; Peterson, RM1
Brady, RO1
al Aqeel, A; al Nasser, M; Blau, N; Brismar, J; Gascon, G; Hughes, H; Nester, M; Ozand, PT; Reynolds, CT; Subramanyan, SB1
Elghozi, JL; Laude, D1
Duch, DS; Nichol, CA; Smith, GK1
Blonder, J; Cohen, BE; Normand, M; Peled, I; Quint, J; Szeinberg, A1
Cavanagh, NP; Hyland, K; Leeming, RJ; Smith, I1
Koprowski, H1
Rauch, H; Siegel, SJ1
Dinsmore, SR; Mrochek, JE; Ohrt, DW1
Andrews, TM; McKeran, RO; McPherson, K; Watts, RW1
Lloyd, J; Smith, I1
Kozik, M1
Bory, P; Jakubovic, A; Woolf, F; Woolf, LI1
Knapp, A; Machill, G; Zehmisch, E1

Reviews

6 review(s) available for phenylalanine and Nervous System Diseases

ArticleYear
Neurological manifestations in adults with phenylketonuria: new cases and review of the literature.
    Journal of neurology, 2020, Volume: 267, Issue:2

    Topics: Adult; Humans; Nervous System Diseases; Phenylalanine; Phenylketonurias; White Matter

2020
Neurological and Neuropsychological Problems in Tyrosinemia Type I Patients.
    Advances in experimental medicine and biology, 2017, Volume: 959

    Topics: Cyclohexanones; Humans; Nervous System Diseases; Nitrobenzoates; Phenylalanine; Tyrosine; Tyrosinemias

2017
Neurophysiological symptoms and aspartame: What is the connection?
    Nutritional neuroscience, 2018, Volume: 21, Issue:5

    Topics: Affect; Animals; Aspartame; Aspartic Acid; Brain; Cognitive Dysfunction; Disease Models, Animal; Dopamine; Free Radicals; Humans; Hydrocortisone; Migraine Disorders; Nervous System Diseases; Neurotransmitter Agents; Non-Nutritive Sweeteners; Norepinephrine; Oxidative Stress; Phenylalanine; Seizures; Serotonin; Sleep Initiation and Maintenance Disorders

2018
Omega-3 LC-PUFA supply and neurological outcomes in children with phenylketonuria (PKU).
    Journal of pediatric gastroenterology and nutrition, 2009, Volume: 48 Suppl 1

    Topics: Child; Child, Preschool; Dietary Supplements; Fatty Acids, Omega-3; Female; Fish Oils; Humans; Infant; Male; Motor Skills; Nervous System Diseases; Nutritional Requirements; Phenylalanine; Phenylketonurias

2009
The role of tetrahydrobiopterin in neurological disease: a review.
    Journal of mental deficiency research, 1981, Volume: 25 Pt 4

    Topics: Aluminum; Biopterins; Brain; Dementia; Humans; Lead Poisoning; Nervous System Diseases; Neurotransmitter Agents; Phenylalanine; Phenylketonurias; Pteridines

1981
Biosynthesis and metabolism of tetrahydrobiopterin and molybdopterin.
    Annual review of biochemistry, 1985, Volume: 54

    Topics: Alcohol Oxidoreductases; Animals; Biopterins; Body Fluids; Coenzymes; GTP Cyclohydrolase; Humans; Immune System Diseases; Mental Disorders; Metalloproteins; Molybdenum; Molybdenum Cofactors; Neoplasms; Nervous System Diseases; Phenylalanine; Phenylketonurias; Pteridines; Pterins; Tetrahydrofolate Dehydrogenase; Tissue Distribution; Tryptophan Hydroxylase; Tyrosine 3-Monooxygenase

1985

Other Studies

24 other study(ies) available for phenylalanine and Nervous System Diseases

ArticleYear
GTP-Cyclohydrolase I deficiency presenting as malignant hyperphenylalaninemia, recurrent hyperthermia and progressive neurological dysfunction in a South Asian child - a case report.
    BMC pediatrics, 2019, 06-15, Volume: 19, Issue:1

    Topics: Brain; Consanguinity; Fever; GTP Cyclohydrolase; Humans; Infant; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Recurrence; Sri Lanka; Vomiting

2019
Neurological improvement following reinstitution of a low phenylalanine diet after 20 years in established phenylketonuria.
    BMJ case reports, 2013, Jul-12, Volume: 2013

    Topics: Adult; Diet; Female; Humans; Nervous System Diseases; Phenylalanine; Phenylketonurias; Time Factors

2013
Altered brain protein expression profiles are associated with molecular neurological dysfunction in the PKU mouse model.
    Journal of neurochemistry, 2014, Volume: 129, Issue:6

    Topics: Animals; Biomarkers; Blotting, Western; Brain Chemistry; Chromatography, High Pressure Liquid; Computational Biology; Computer Simulation; Disease Models, Animal; Electrophoresis, Gel, Two-Dimensional; Gene Regulatory Networks; Mice; Nervous System Diseases; Phenylalanine; Phenylketonurias; Protein Biosynthesis; Tandem Mass Spectrometry

2014
Routine use of CANTAB system for detection of neuropsychological deficits in patients with PKU.
    Molecular genetics and metabolism, 2011, Volume: 102, Issue:2

    Topics: Adolescent; Adult; Female; Humans; Male; Nervous System Diseases; Neuropsychological Tests; Phenylalanine; Phenylketonurias; Treatment Outcome; Young Adult

2011
Long-term outcome and neuroradiological findings of 31 patients with 6-pyruvoyltetrahydropterin synthase deficiency.
    Journal of inherited metabolic disease, 2006, Volume: 29, Issue:1

    Topics: Brain; Brain Diseases, Metabolic, Inborn; Child, Preschool; Developmental Disabilities; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Nervous System Diseases; Phenylalanine; Phosphorus-Oxygen Lyases; Time Factors; Treatment Outcome

2006
Diagnostic and therapeutic aspects of dihydrobiopterin deficiency.
    Acta paediatrica Scandinavica, 1983, Volume: 72, Issue:3

    Topics: 5-Hydroxytryptophan; Biopterins; Carbidopa; Chromatography, High Pressure Liquid; Dihydroxyphenylalanine; Humans; Infant; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Pteridines

1983
[Phenylketonuria with adult-onset neurological manifestation].
    Rinsho shinkeigaku = Clinical neurology, 1993, Volume: 33, Issue:9

    Topics: Adult; Brain; Humans; Magnetic Resonance Imaging; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Quadriplegia; Visual Fields

1993
Maternal Phenylketonuria Collaborative Study (MPKUCS) offspring: facial anomalies, malformations, and early neurological sequelae.
    American journal of medical genetics, 1997, Mar-03, Volume: 69, Issue:1

    Topics: Cohort Studies; Cooperative Behavior; Face; Female; Humans; Nervous System; Nervous System Diseases; Nervous System Malformations; Phenylalanine; Phenylketonuria, Maternal; Pregnancy

1997
Intellectual, neurologic, and neuropsychologic outcome in untreated subjects with nonphenylketonuria hyperphenylalaninemia. German Collaborative Study on Phenylketonuria.
    Pediatric research, 1997, Volume: 42, Issue:3

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Attention; Career Choice; Data Interpretation, Statistical; Female; Genotype; Humans; Intelligence; Job Satisfaction; Learning Disabilities; Magnetic Resonance Imaging; Male; Movement Disorders; Nervous System Diseases; Neurotic Disorders; Phenotype; Phenylalanine; Phenylketonurias; Problem Solving; Psychomotor Performance; Tremor

1997
Dihydropteridine reductase deficiency associated with severe neurologic disease and mild hyperphenylalaninemia.
    Pediatrics, 1979, Volume: 63, Issue:1

    Topics: 5-Hydroxytryptophan; Ascorbic Acid; Consanguinity; Dopamine; Humans; Infant; Levodopa; Liver; Male; NADH, NADPH Oxidoreductases; Nervous System Diseases; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Serotonin

1979
Congenital and neurological abnormalities in infants with phenylketonuria.
    American journal of mental deficiency, 1978, Volume: 82, Issue:4

    Topics: Abnormalities, Multiple; Female; Humans; Infant; Infant, Newborn; Longitudinal Studies; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Pyloric Stenosis; United States

1978
Inherited metabolic diseases of the nervous system.
    Science (New York, N.Y.), 1976, Aug-27, Volume: 193, Issue:4255

    Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Gangliosidoses; Glutathione; Glycine; Glycogen Storage Disease Type II; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nerve Tissue Proteins; Nervous System Diseases; Phenylalanine; Phenylketonurias

1976
Biopterin-dependent hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase.
    Neurology, 1991, Volume: 41, Issue:5

    Topics: Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Biopterins; Female; Humans; Infant; Male; Nervous System Diseases; Phenylalanine; Phosphorus-Oxygen Lyases; Saudi Arabia

1991
[5-HIAA: perspectives in nephrology].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1989, Volume: 183, Issue:1

    Topics: Animals; Carcinoid Tumor; Humans; Hydroxyindoleacetic Acid; Intestinal Mucosa; Kidney; Metabolic Clearance Rate; Migraine Disorders; Nervous System Diseases; p-Aminohippuric Acid; Phenylalanine; Rats; Renal Circulation; Serotonin

1989
Malignant phenylketonuria due to defective synthesis of dihydrobiopterin.
    Israel journal of medical sciences, 1985, Volume: 21, Issue:6

    Topics: 5-Hydroxytryptophan; Biopterins; Carbidopa; Drug Combinations; Female; Humans; Infant, Newborn; Levodopa; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Pteridines; Tyrosine

1985
Neurological aspects of biopterin metabolism.
    Archives of disease in childhood, 1986, Volume: 61, Issue:2

    Topics: Adolescent; Biological Assay; Biopterins; Child; Child, Preschool; Dystonia Musculorum Deformans; Humans; Infant; Male; Nervous System Diseases; Phenylalanine; Phenylketonurias; Pteridines

1986
Chronic viral neuropathies: models for study and food for thought.
    International archives of allergy and applied immunology, 1969, Volume: 36

    Topics: Animals; Antiviral Agents; Cattle; Chick Embryo; Cricetinae; Cytarabine; Cytomegalovirus; Dactinomycin; Deoxyuridine; Disease Models, Animal; DNA, Viral; Encephalitis Viruses; Friend murine leukemia virus; Humans; Imidazoles; Interferons; Mice; Mitomycins; Nervous System Diseases; Parainfluenza Virus 1, Human; Phenylalanine; Prions; Respirovirus; RNA Viruses; RNA, Viral; Vesicular stomatitis Indiana virus; Viral Interference; Virus Diseases

1969
Aromatic amino acid metabolism in the wabbler-lethal mouse.
    Biochemical genetics, 1969, Volume: 2, Issue:4

    Topics: Aging; Animals; Liver; Mice; Mixed Function Oxygenases; Nervous System Diseases; Phenylalanine; Rodent Diseases; Transaminases; Tryptophan; Tryptophan Oxygenase; Tyrosine; Tyrosine Transaminase

1969
Monitoring phenylalanine-tyrosine metabolism by high-resolution liquid chromatography of urine.
    Clinical chemistry, 1973, Volume: 19, Issue:8

    Topics: Aromatic Amino Acid Decarboxylase Inhibitors; Autistic Disorder; Carbidopa; Catechols; Child; Chromatography, Gas; Chromatography, Ion Exchange; Dihydroxyphenylalanine; Hippurates; Homovanillic Acid; Humans; Hyperkinesis; Intellectual Disability; Lactates; Mandelic Acids; Mass Spectrometry; Methods; Nervous System Diseases; Parkinson Disease; Phenylacetates; Phenylalanine; Spectrophotometry, Ultraviolet; Tyrosine

1973
Relation between granulocyte phenylalanine content and degree of neuropsychiatric disability in phenylketonuria.
    Archives of disease in childhood, 1973, Volume: 48, Issue:8

    Topics: Humans; Leukocytes; Nervous System Diseases; Phenylalanine; Phenylketonurias

1973
Proceedings: Atypical phenylketonuria accompanied by a severe progressive neurological illness unresponsive to dietary treatment.
    Archives of disease in childhood, 1974, Volume: 49, Issue:3

    Topics: Biopsy; Diet Therapy; Humans; Liver; Movement Disorders; Nervous System Diseases; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias; Social Behavior

1974
Degenerative changes of neurocytes in the light of autoradiographic investigations.
    Pathologia Europaea, 1971, Volume: 6, Issue:2

    Topics: Adenine; Amino Acids; Animals; Autoradiography; Brain; Carbon Isotopes; Cerebral Cortex; Disease Models, Animal; Female; Glycine; Leucine; Male; Nerve Degeneration; Nerve Tissue Proteins; Nervous System Diseases; Neurons; Nucleoproteins; Phenylalanine; Radiation Injuries, Experimental; Rats; Rats, Inbred Strains; Sciatic Nerve; Thymidine; Tritium

1971
Metabolism of phenylalanine in mice homozygous for the gene 'dilute lethal'.
    The Biochemical journal, 1970, Volume: 119, Issue:5

    Topics: Animals; Disease Models, Animal; Female; Genes, Lethal; Homozygote; Humans; Liver; Male; Mice; Mixed Function Oxygenases; Nervous System Diseases; Organ Size; Phenylalanine; Phenylketonurias; Phenylpyruvic Acids

1970
[Studies on the frequency of phenylketonuria using the Guthrie microbial screening test].
    Psychiatrie, Neurologie, und medizinische Psychologie, 1969, Volume: 21, Issue:5

    Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Enuresis; Epilepsy; Female; Germany, East; Humans; Infant; Male; Mass Screening; Methods; Middle Aged; Nervous System Diseases; Neurocognitive Disorders; Phenylalanine; Phenylketonurias; Sex Factors; Syphilis

1969