phenylalanine and Huntington Disease

phenylalanine has been researched along with Huntington Disease in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19903 (50.00)18.7374
1990's2 (33.33)18.2507
2000's0 (0.00)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Burman, J; Emami Khoonsari, P; Herman, S; Kultima, K; Landtblom, AM; Niemelä, V; Nyholm, D; Spjuth, O; Sundblom, J1
Lange, HW; Reilmann, R; Rolf, LH1
Kuncl, RW; Martin, LJ; Rothstein, JD1
Gerstenbrand, F; Gründig, E; Schedl, R; Simanyi, M; Weiss, H1
Ottosson, JO; Rapp, W1
Brodie, KH; Chase, TN; Donnelly, EF; Watanabe, AM1

Other Studies

6 other study(ies) available for phenylalanine and Huntington Disease

ArticleYear
Alterations in the tyrosine and phenylalanine pathways revealed by biochemical profiling in cerebrospinal fluid of Huntington's disease subjects.
    Scientific reports, 2019, 03-11, Volume: 9, Issue:1

    Topics: Adult; Aged; Biomarkers; Dopamine; Female; Humans; Huntington Disease; Levodopa; Male; Middle Aged; Phenylalanine; Thyroxine; Tyrosine

2019
Huntington's disease: the neuroexcitotoxin aspartate is increased in platelets and decreased in plasma.
    Journal of the neurological sciences, 1994, Dec-01, Volume: 127, Issue:1

    Topics: Adult; Aspartic Acid; Blood Platelets; Blood Proteins; Chromatography, High Pressure Liquid; Female; Glutamic Acid; Glutamine; Humans; Huntington Disease; Male; Middle Aged; Phenylalanine; Plasma

1994
Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis.
    The New England journal of medicine, 1992, May-28, Volume: 326, Issue:22

    Topics: Aged; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Biological Transport; Brain; Female; gamma-Aminobutyric Acid; Glutamates; Glutamic Acid; Humans; Huntington Disease; In Vitro Techniques; Male; Middle Aged; Motor Cortex; Phenylalanine; Somatosensory Cortex; Spinal Cord; Synaptosomes; Visual Cortex

1992
[Effect of administration of amino acids, especially of L-DOPA and -methyldopa, on the composition of cerebrospinal fluid in extrapyramidal syndromes. 3. Alterations of cerebrospinal fluid in patients with Huntington's chorea after -methyldopa or L-DOPA
    Zeitschrift fur Neurologie, 1973, Mar-16, Volume: 204, Issue:1

    Topics: Adult; Aged; Alanine Transaminase; Asparagine; Aspartic Acid; Child; Dihydroxyphenylalanine; Female; Glutamates; Glutamine; Glycine; Humans; Huntington Disease; Male; Methyldopa; Middle Aged; Phenylalanine; Pyruvates; Threonine

1973
Serum levels of phenylalanine and tyrosine in Huntington's chorea.
    Acta psychiatrica Scandinavica. Supplementum, 1971, Volume: 221

    Topics: Adult; Aged; Analysis of Variance; Antidepressive Agents; Body Weight; Dopamine; Female; Humans; Huntington Disease; Male; Middle Aged; Norepinephrine; Parasympatholytics; Phenylalanine; Psychotic Disorders; Reserpine; Schizophrenia; Tryptophan; Tyrosine

1971
Huntington's chorea. Effect of serotonin depletion.
    Archives of neurology, 1972, Volume: 26, Issue:3

    Topics: Adult; Dopamine; Female; Humans; Huntington Disease; Hydroxyindoleacetic Acid; Intelligence; Male; Middle Aged; Motor Skills; Phenylacetates; Phenylalanine; Serotonin; Serotonin Antagonists

1972