methionine has been researched along with Amyloid Neuropathies in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 10 (66.67) | 18.2507 |
2000's | 3 (20.00) | 29.6817 |
2010's | 2 (13.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ericzon, BG; Nowak, G; Suhr, OB; Westermark, P | 1 |
Boukhris, S; Diallo, L; Magy, L; Mathis, S; Vallat, JM | 1 |
Ikeda, S; Mitsuhashi, S; Tokuda, T; Yamamoto, K; Yazaki, M | 1 |
Heldestad, V; Nordh, E | 1 |
Cambi, F; Strocchi, P; Tang, XM | 1 |
Andersson, C; Asplund, K; Beckman, L; Costa, PM; Costa, PP; Holmgren, G; Nylander, PO; Saraiva, MJ; Steen, L; Teixeira, A | 1 |
Ii, S; Sommer, SS | 1 |
Adams, D; Davis, MB; Harding, AE; Reilly, MM; Said, G | 1 |
Ando, M; Ando, Y; Ferlini, A; Gobbi, P; Nakamura, M; Patrosso, C; Salvi, F; Tanaka, Y; Uchino, M; Yamashita, T | 1 |
Bonavita, V; Di Iorio, G; Sampaolo, S; Sanges, G | 1 |
Anan, I; Ando, Y; Costa, PM; Holmgren, G; Suhr, O | 1 |
Ando, E; Ando, M; Ando, Y; Lundgren, E; Negi, A; Obayashi, K; Ohlsson, PI; Olofsson, A; Sandgren, O; Suhr, O; Terazaki, H | 1 |
Ando, Y; Holmgren, G; Obayashi, K; Suhr, OB; Tashima, K; Terazaki, H; Uchino, M; Yamashita, T | 1 |
Baba, T; Date, Y; Goto, Y; Nakamura, Y; Nakazato, M; Yutani, C | 1 |
Araki, S; Yi, S | 1 |
15 other study(ies) available for methionine and Amyloid Neuropathies
Article | Year |
---|---|
Domino liver transplantation: full-length transthyretin in donor and recipient patients with ATTR Val30Met amyloidosis.
Topics: Adult; Aged; Amyloid Neuropathies; Amyloid Neuropathies, Familial; Amyloidosis; Female; Humans; Liver Transplantation; Male; Methionine; Middle Aged; Valine | 2017 |
Amyloid neuropathy mimicking chronic inflammatory demyelinating polyneuropathy.
Topics: Aged; Aged, 80 and over; Amyloid Neuropathies; Biopsy; Electromyography; Female; Humans; Male; Methionine; Mutation; Neural Conduction; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating; Prealbumin; Sural Nerve; Valine | 2012 |
MRI analysis on a patient with the V30M mutation is characteristic of leptomeningeal amyloid.
Topics: Amino Acid Substitution; Amyloid Neuropathies; Brain; Cataract; Gadolinium; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Point Mutation; Prealbumin; Radiography; Spinal Cord; Valine | 2004 |
Quantified sensory abnormalities in early genetically verified transthyretin amyloid polyneuropathy.
Topics: Adult; Age Factors; Amyloid Neuropathies; Female; Humans; Male; Methionine; Peripheral Nerves; Prealbumin; Sensory Thresholds; Somatosensory Disorders; Temperature; Valine | 2007 |
Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy.
Topics: Amyloid Neuropathies; Base Sequence; DNA Primers; Female; Humans; Italy; Male; Methionine; Molecular Sequence Data; Mutation; Pedigree; Prealbumin | 1995 |
Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate.
Topics: Adult; Aged; Alleles; Amyloid Neuropathies; Enzyme-Linked Immunosorbent Assay; Female; Gene Frequency; Genetic Carrier Screening; Humans; Male; Methionine; Middle Aged; Molecular Epidemiology; Mutation; Prealbumin; Predictive Value of Tests; Prevalence; Sweden | 1994 |
The high frequency of TTR M30 in familial amyloidotic polyneuropathy is not due to a founder effect.
Topics: Amino Acid Sequence; Amyloid Neuropathies; DNA; Genes, Dominant; Haplotypes; Humans; Methionine; North America; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Prealbumin; Valine | 1993 |
Haplotype analysis of French, British and other European patients with familial amyloid polyneuropathy (met 30 and tyr 77).
Topics: Amyloid Neuropathies; Base Sequence; Europe; France; Genes, Dominant; Haplotypes; Humans; Methionine; Molecular Sequence Data; Mutation; Polymorphism, Genetic; Tyrosine; United Kingdom | 1995 |
Decreased affinity of apolipoprotein AII to high-density lipoprotein in patients with transthyretin-related amyloidosis (Met30, Gln89, Pro36, and Thr34).
Topics: Amino Acid Sequence; Amyloid Neuropathies; Apolipoprotein A-I; Apolipoprotein A-II; Cholesterol; Cholesterol Esters; Gene Expression; Glutamine; Humans; Lipoproteins, HDL; Liver; Methionine; Phospholipids; Point Mutation; Prealbumin; Proline; Reference Values; Threonine; Triglycerides | 1996 |
A comment on: 'Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy' by Paola Strocchi et al., FEBS Letters 359 (1995) 203-205.
Topics: Amyloid Neuropathies; Female; Humans; Italy; Male; Methionine; Mutation; Pedigree; Prealbumin | 1996 |
Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy.
Topics: Adult; Amyloid Neuropathies; Biomarkers; Female; Hair; Humans; Immunologic Tests; Male; Methionine; Middle Aged; Prealbumin | 1998 |
Analysis of transthyretin amyloid fibrils from vitreous samples in familial amyloidotic polyneuropathy (Val30Met).
Topics: Aged; Amino Acid Substitution; Amyloid Neuropathies; Female; Humans; Male; Methionine; Middle Aged; Molecular Weight; Prealbumin; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Valine; Vitreous Body | 1999 |
Gastrointestinal dysfunction in familial amyloidotic polyneuropathy (ATTR Val30Met)--comparison of Swedish and Japanese patients.
Topics: Adolescent; Adult; Age of Onset; Aged; Amino Acid Substitution; Amyloid Neuropathies; Digestive System; Female; Humans; Japan; Male; Methionine; Middle Aged; Prealbumin; Sweden; Valine | 1999 |
A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
Topics: Aged; Amyloid Neuropathies; Amyloidosis; Base Sequence; Cardiomyopathies; Female; Giant Cells; Heart Ventricles; Humans; Methionine; Point Mutation; Prealbumin; Rectum | 1999 |
Pathology of familial amyloidotic polyneuropathy with TTR met 30 in Kumamoto, Japan.
Topics: Adult; Amyloid; Amyloid Neuropathies; Animals; Disease Models, Animal; Female; Humans; Japan; Male; Methionine; Mice; Mice, Transgenic; Middle Aged; Nerve Fibers; Point Mutation; Prealbumin; Sural Nerve | 2000 |