Compounds > phenylalanine

phenylalanine and Amyloid Neuropathies, Familial

phenylalanine has been researched along with Amyloid Neuropathies, Familial in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Björkenheim, A; Szabó, B; Sztaniszláv, ÁJ1
Meredith, SC; Orgel, JP; Sciarretta, KL; Tycko, R1
Abe, K; Ando, Y; Fujii, D; Kono, S; Manabe, Y; Narai, H; Omori, N; Sakai, Y; Tanaka, T; Ueda, M1
Hellman, U; Holmgren, G; Jonasson, J; Lundgren, HE; Suhr, OB; Westermark, P1

Reviews

1 review(s) available for phenylalanine and Amyloid Neuropathies, Familial

ArticleYear
A case of familial amyloid polyneuropathy due to Phe33Val TTR with vitreous involvement as the initial manifestation.
    Internal medicine (Tokyo, Japan), 2010, Volume: 49, Issue:12

    Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Diagnosis, Differential; Eye Diseases; Female; Humans; Middle Aged; Phenylalanine; Prealbumin; Valine; Vitreous Body

2010

Other Studies

3 other study(ies) available for phenylalanine and Amyloid Neuropathies, Familial

ArticleYear
Hereditary transthyretin amyloidosis caused by the rare Phe33Leu mutation.
    BMJ case reports, 2020, Jan-12, Volume: 13, Issue:1

    Topics: Amyloid Neuropathies, Familial; Benzoxazoles; Combined Modality Therapy; Diagnosis, Differential; Heart Transplantation; Humans; Leucine; Male; Middle Aged; Mutation; Phenylalanine; Prealbumin

2020
Evidence for novel beta-sheet structures in Iowa mutant beta-amyloid fibrils.
    Biochemistry, 2009, Jul-07, Volume: 48, Issue:26

    Topics: Amyloid; Amyloid beta-Peptides; Amyloid Neuropathies, Familial; Aspartic Acid; Benzothiazoles; Glutamic Acid; Humans; Kinetics; Leucine; Lysine; Microscopy, Electron, Transmission; Models, Molecular; Mutation, Missense; Nuclear Magnetic Resonance, Biomolecular; Peptide Fragments; Phenylalanine; Protein Structure, Secondary; Spectrometry, Fluorescence; Thiazoles; X-Ray Diffraction

2009
A Swedish family with the rare Phe33Leu transthyretin mutation.
    Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2005, Volume: 12, Issue:3

    Topics: Amyloid Neuropathies, Familial; Carpal Tunnel Syndrome; Female; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Phenotype; Phenylalanine; Prealbumin; Sweden

2005