glutamic acid has been researched along with Amyloid Neuropathy Type 1 in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (63.64) | 29.6817 |
| 2010's | 3 (27.27) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Gospodinova, M; Kirov, A; Nakov, R; Nakov, V; Sarafov, S; Todorov, T; Todorova, A; Tournev, I | 1 |
| Bollati, M; de Rosa, M; Drnovšek-Olup, B; Fakin, A; Gornik, A; Hawlina, M; Hočevar, A; Jaklič, H; Maver, A; Peterlin, B; Pfeifer, V; Pižem, J; Potrč, M; Teran, N; Vogelnik, K; Volk, M | 1 |
| Chamova, T; Gospodinova, M; Kirov, A; Mitev, V; Pavlova, Z; Sarafov, S; Todorov, T; Todorova, A; Tournev, I | 1 |
| Acker, T; Haverkamp, T; Kimmich, C; Krämer, HH; Röcken, C; Schänzer, A; Weidner, I | 1 |
| Meredith, SC; Orgel, JP; Sciarretta, KL; Tycko, R | 1 |
| Benson, MD; Bybee, A; Haagsma, EB; Hawkins, PN; Hazenberg, BP; Lachmann, HJ | 1 |
| Choi, YC; Jung, SC; Kang, SW; Kim, HS; Kim, SM; Kim, TS; Lee, KS | 1 |
| Connors, LH; Costello, C; Drachman, BM; Prokaeva, T; Rosenzweig, M; Skinner, M; Théberge, R | 1 |
| Fawzi, A; He, S; Lim, JI; O'Hearn, TM; Rao, NA | 1 |
| Baranov, V; Hörstedt, P; Ippel, HJ; Lundgren, E; Olofsson, A; Wijmenga, S | 1 |
| Castelli, G; Ciaccheri, M; Da Prato, L; Gori, F; Marconi, G; Pelo, E; Pizzi, A; Torricelli, F | 1 |
11 other study(ies) available for glutamic acid and Amyloid Neuropathy Type 1
| Article | Year |
|---|---|
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln Mutation.
Topics: Adult; Aged; Amyloid Neuropathies, Familial; Diarrhea; Female; Gastrointestinal Diseases; Glutamic Acid; Glutamine; Humans; Kaplan-Meier Estimate; Male; Middle Aged; Mutation; Nausea; Prealbumin; Prospective Studies; Weight Loss | 2019 |
Clinical and Histopathological Features of Gelsolin Amyloidosis Associated with a Novel
Topics: Adult; Aged; Amyloid Neuropathies, Familial; Amyloidosis; Amyloidosis, Familial; Corneal Diseases; Corneal Dystrophies, Hereditary; Exome; Family Health; Female; Fundus Oculi; Gelsolin; Genetic Association Studies; Glutamic Acid; Humans; Lysine; Male; Middle Aged; Mutation; Optic Nerve; Optic Nerve Diseases; Phenotype; Protein Folding; Tomography, Optical Coherence | 2021 |
Founder effect of the Glu89Gln
Topics: Adult; Aged; Amyloid Neuropathies, Familial; Bulgaria; Female; Founder Effect; Glutamic Acid; Glutamine; Haplotypes; Humans; Male; Microsatellite Repeats; Middle Aged; Mutation; Prealbumin | 2019 |
A woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report.
Topics: Adult; Amyloid Neuropathies, Familial; Benzoxazoles; Disease Progression; Fatal Outcome; Female; Genetic Linkage; Glutamic Acid; Glycine; Humans; Liver Transplantation; Mutation, Missense; Pedigree; Prealbumin | 2014 |
Evidence for novel beta-sheet structures in Iowa mutant beta-amyloid fibrils.
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 |
Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families.
Topics: Aged; Amino Acid Substitution; Amyloid Neuropathies, Familial; Family; Female; Glutamic Acid; Glycine; Humans; Liver Transplantation; Male; Middle Aged; Netherlands; Pedigree; Prealbumin; Radiography; United Kingdom; United States; White People | 2004 |
An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene.
Topics: Amyloid Neuropathies, Familial; DNA Mutational Analysis; Family Health; Female; Glutamic Acid; Glycine; Humans; Male; Mutation; Nerve Fibers, Myelinated; Prealbumin; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2005 |
A new transthyretin variant (Glu61Gly) associated with cardiomyopathy.
Topics: Amino Acid Substitution; Amyloid Neuropathies, Familial; Base Sequence; Cardiomyopathies; DNA Mutational Analysis; Glutamic Acid; Glycine; Humans; Isoelectric Focusing; Male; Mass Screening; Mass Spectrometry; Middle Aged; Molecular Sequence Data; Prealbumin | 2007 |
Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.
Topics: Adult; Age of Onset; Amyloid Neuropathies, Familial; Asian People; Eye Diseases, Hereditary; Fluorescein Angiography; Fundus Oculi; Glutamic Acid; Glycine; Humans; Male; Mutation; Prealbumin; Vascular Endothelial Growth Factor A; Vitrectomy; Vitreous Body | 2007 |
Capture of a dimeric intermediate during transthyretin amyloid formation.
Topics: Amyloid; Amyloid Neuropathies, Familial; Anilino Naphthalenesulfonates; Asparagine; Dimerization; Fluorescent Dyes; Glutamic Acid; Guanidine; Humans; Models, Molecular; Mutation; Prealbumin; Protein Binding; Protein Denaturation; Protein Folding; Protein Structure, Secondary; Recombinant Proteins; Staining and Labeling; Temperature; Thyroxine; Valine | 2001 |
Familial amyloid polyneuropathy with genetic anticipation associated to a gly47glu transthyretin variant in an Italian kindred.
Topics: Adult; Amino Acid Sequence; Amyloid Neuropathies, Familial; Base Sequence; DNA; Female; Glutamic Acid; Glycine; Humans; Italy; Male; Middle Aged; Pedigree; Point Mutation; Prealbumin | 2002 |