phenylalanine and Akinetic-Rigid Variant of Huntington Disease

phenylalanine has been researched along with Akinetic-Rigid Variant of 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 Akinetic-Rigid Variant of 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