Compounds > phenylalanine

phenylalanine and Peripheral Nerve Diseases

phenylalanine has been researched along with Peripheral Nerve Diseases in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hayes, DF; Henry, NL; Hertz, DL; Kim, JH; Smith, EML; Stringer, KA; Sun, Y; Vangipuram, K; Yeomans, L1
Bönnemann, C; Brockmann, K; Gärtner, J; Huebner, A; Kind, B; Koehler, K; Krumbholz, M1
Benson, MD; Dupond, JL; Gil, H; Kantelip, B; Kluve-Beckerman, B; Liepnieks, JJ; Magy, N1
Christodoulou, K; Georgiou, DM; Kleopa, KA; Koutsou, P; Kyriakides, T; Nicolaou, P; Papathanasiou, E1
Bourre, JM; Fournier, E; Fournier, LE; Lecorsier, A1

Other Studies

5 other study(ies) available for phenylalanine and Peripheral Nerve Diseases

ArticleYear
Pharmacometabolomics reveals a role for histidine, phenylalanine, and threonine in the development of paclitaxel-induced peripheral neuropathy.
    Breast cancer research and treatment, 2018, Volume: 171, Issue:3

    Topics: Adult; Aged; Biomarkers; Breast Neoplasms; Female; Histidine; Humans; Magnetic Resonance Spectroscopy; Metabolomics; Middle Aged; Paclitaxel; Peripheral Nervous System Diseases; Phenylalanine; Threonine

2018
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.
    European journal of human genetics : EJHG, 2008, Volume: 16, Issue:12

    Topics: Amino Acid Substitution; DNA Mutational Analysis; Female; HeLa Cells; Humans; Lacrimal Apparatus Diseases; Leucine; Muscular Atrophy; Musculoskeletal Abnormalities; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Syndrome; Transfection

2008
A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:1

    Topics: Aged; Amyloidosis; Base Sequence; Carpal Tunnel Syndrome; Humans; Male; Pedigree; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Polymorphism, Single-Stranded Conformational; Prealbumin; Skin; Tyrosine

2003
A novel PMP22 mutation Ser22Phe in a family with hereditary neuropathy with liability to pressure palsies and CMT1A phenotypes.
    Neurogenetics, 2004, Volume: 5, Issue:3

    Topics: Adult; Charcot-Marie-Tooth Disease; Electrophysiology; Exons; Family Health; Female; Genetic Predisposition to Disease; Humans; Male; Mutation; Myelin Proteins; Neurons; Pedigree; Peripheral Nervous System Diseases; Phenotype; Phenylalanine; Point Mutation; Sequence Analysis, DNA; Serine

2004
[Lymphocyte phenylvaleric acid hydroxylase activity (L-PVH), a new marker of peripheral neurotoxicity].
    Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie, 1992, Volume: 315, Issue:10

    Topics: Adult; Biomarkers; Carboxylic Ester Hydrolases; Diabetic Neuropathies; Humans; Lymphocytes; Mixed Function Oxygenases; Peripheral Nervous System Diseases; Phenylalanine; Valerates

1992