Compounds > phenylalanine

phenylalanine and Parkinsonian Disorders

phenylalanine has been researched along with Parkinsonian Disorders in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Asselta, R; Blau, N; Cilia, R; Duga, S; Farrer, MJ; Follett, J; Goldwurm, S; Guella, I; Hattori, N; Nishioka, K; Parkkinen, L; Pezzoli, G; Priori, A; Rajput, A; Rajput, AH; Rimoldi, V; Soldà, G; Sossi, V; Stoessl, AJ; Straniero, L; Young, A1
Arai, K; Asahina, M; Funayama, M; Hattori, N; Hattori, T; Kanai, K; Kuwabara, S; Kuwabara, Y; Sekiguchi, Y; Tomiyama, H; Uchiyama, T1
Dawson, TM; Dawson, VL; Moore, DJ; Zhang, L1
Blau, N; Casaer, P; Goriounov, D; Hedrich, K; Klein, C; Legius, E; Matthijs, G; Møller, LB; Romstad, A; Steyaert, J; Theys, P; Van Hove, JL; Wevers, R1
Rodacker, V; Toustrup-Jensen, M; Vilsen, B1

Other Studies

5 other study(ies) available for phenylalanine and Parkinsonian Disorders

ArticleYear
DNAJC12 and dopa-responsive nonprogressive parkinsonism.
    Annals of neurology, 2017, Volume: 82, Issue:4

    Topics: Adult; alpha-Synuclein; Amyloid beta-Peptides; Antiparkinson Agents; Biogenic Amines; Brain; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Female; Humans; Levodopa; Male; Middle Aged; Mutation; Parkinsonian Disorders; Phenylalanine; Repressor Proteins; Sequestosome-1 Protein; tau Proteins; Young Adult

2017
Preserved cardiac (123)I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Jul-15, Volume: 24, Issue:9

    Topics: 3-Iodobenzylguanidine; Adult; Autonomic Nervous System Diseases; Heart; Humans; Leucine; Male; Myocardium; Parkinsonian Disorders; Phenylalanine; Proton-Translocating ATPases; Radionuclide Imaging; Young Adult

2009
A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization.
    Journal of neurochemistry, 2003, Volume: 87, Issue:6

    Topics: Autoantigens; Blotting, Northern; Blotting, Western; Cell Line, Tumor; Cycloheximide; Electrophoresis, Gel, Pulsed-Field; Humans; In Vitro Techniques; Intracellular Signaling Peptides and Proteins; Leucine; Methionine; Mutation, Missense; Oncogene Proteins; Parkinsonian Disorders; Phenylalanine; Precipitin Tests; Protein Deglycase DJ-1; Protein Synthesis Inhibitors; Proteins; Proto-Oncogene Proteins c-myc; Ribonucleoproteins; RNA, Messenger; SS-B Antigen; Sulfur Isotopes; Transfection

2003
Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.
    Journal of neurology, neurosurgery, and psychiatry, 2006, Volume: 77, Issue:1

    Topics: Adolescent; Adult; Circadian Rhythm; Dystonia; Female; Fibroblasts; Gene Expression; GTP Cyclohydrolase; Humans; Lower Extremity; Male; Middle Aged; Paraparesis, Spastic; Parkinsonian Disorders; Pedigree; Phenotype; Phenylalanine; Polymerase Chain Reaction; Reflex, Abnormal; Syndrome; Tendinopathy; Tremor

2006
Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.
    The Journal of biological chemistry, 2006, Jul-07, Volume: 281, Issue:27

    Topics: Animals; Chlorocebus aethiops; COS Cells; Dystonia; Genetic Predisposition to Disease; Humans; Models, Molecular; Mutation; Parkinsonian Disorders; Phenylalanine; Protein Conformation; Rats; Sodium; Sodium-Potassium-Exchanging ATPase; Threonine

2006