Compounds > phenylalanine

phenylalanine and Amyloid Neuropathy Type 1

phenylalanine has been researched along with Amyloid Neuropathy Type 1 in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	1 (25.00)	24.3611
2020's	1 (25.00)	2.80

Authors

Authors	Studies
Björkenheim, A; Szabó, B; Sztaniszláv, ÁJ	1
Meredith, SC; Orgel, JP; Sciarretta, KL; Tycko, R	1
Abe, K; Ando, Y; Fujii, D; Kono, S; Manabe, Y; Narai, H; Omori, N; Sakai, Y; Tanaka, T; Ueda, M	1
Hellman, U; Holmgren, G; Jonasson, J; Lundgren, HE; Suhr, OB; Westermark, P	1

Reviews

1 review(s) available for phenylalanine and Amyloid Neuropathy Type 1

Article	Year
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 Neuropathy Type 1

Article	Year
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