tyrosine has been researched along with Peripheral Nervous System Diseases in 13 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (7.69) | 18.7374 |
1990's | 5 (38.46) | 18.2507 |
2000's | 3 (23.08) | 29.6817 |
2010's | 4 (30.77) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Audano, M; Azcoitia, I; Carozzi, V; Caruso, D; Cavaletti, G; Cermenati, G; Crestani, M; D'Antonio, M; De Fabiani, E; Ferri, C; Garcia-Segura, LM; Giatti, S; Melcangi, RC; Mitro, N; Pettinato, E; Porretta-Serapiglia, C; Saez, E; Scurati, S | 1 |
Cabrini, DI; Herrera, RF; Lavigne Moreira, C; Lourenço, CM; Marques, VD; Marques, W; Nuñez, JC | 1 |
Blake, J; Carr, AS; Evans, MR; Gillmore, JD; Hawkins, PN; Iodice, V; Laurà, M; Pelayo-Negro, AL; Reilly, MM; Stancanelli, C; Wechalekar, AD; Whelan, CJ | 1 |
Areti, A; Gogoi, R; Komirishetty, P; Kumar, A; Ruby, PK; Sharma, SS; Sistla, R; Yerra, VG | 1 |
Benson, MD; Dupond, JL; Gil, H; Kantelip, B; Kluve-Beckerman, B; Liepnieks, JJ; Magy, N | 1 |
Abe, T; Hattori, K; Ito, S; Katano, T; Mabuchi, T; Matsumura, S; Mishina, M; Nakai, Y; Nakazawa, T; Takagi, K; Watanabe, M; Xu, L; Yagi, T; Yamamoto, A; Yamamoto, T | 1 |
Derenko, MV; Grzybowski, T; Malyarchuk, BA; Miścicka-Sliwka, D; Stopińska, K | 1 |
Hayashi, A; Higa, S; Nakajima, A; Sakoda, S; Suzuki, T; Takaba, Y; Yamamura, Y | 1 |
Bailey, S; Barnes, ND; Clayton, P; Jamieson, N; Noble-Jamieson, G; Ryalls, M | 1 |
Brett, EM; Clayton, PT; Gibbs, TC; Holme, E; Lindstedt, S; Payan, J | 1 |
Kumada, S; Okaniwa, M | 1 |
Gauthier, M; Grenier, A; Lacroix, J; Lambert, M; Larbrisseau, A; Larochelle, J; Michaud, J; Mitchell, G; Ogier, H; Vanasse, M | 1 |
Tarui, S; Uemichi, T; Ueno, S; Yorifuji, S | 1 |
1 review(s) available for tyrosine and Peripheral Nervous System Diseases
Article | Year |
---|---|
[Progressive neuronal degeneration and childhood cirrhosis].
Topics: Galactosemias; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Metabolism, Inborn Errors; Peripheral Nervous System Diseases; Tyrosine | 1995 |
12 other study(ies) available for tyrosine and Peripheral Nervous System Diseases
Article | Year |
---|---|
Lack of sterol regulatory element binding factor-1c imposes glial Fatty Acid utilization leading to peripheral neuropathy.
Topics: Analysis of Variance; Animals; Blotting, Western; Chromatography, High Pressure Liquid; Fatty Acids; Metabolomics; Mice; Mice, Knockout; Microarray Analysis; Microscopy, Electron, Transmission; Myelin Sheath; Neuroglia; Oxazoles; Peripheral Nervous System Diseases; PPAR alpha; Real-Time Polymerase Chain Reaction; Sterol Regulatory Element Binding Protein 1; Tyrosine | 2015 |
Transthyretin Asp38Tyr: a new mutation associated to a late onset neuropathy.
Topics: Aged; Aspartic Acid; Female; Humans; Mutation; Peripheral Nervous System Diseases; Prealbumin; Tyrosine | 2015 |
A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK.
Topics: Adenine; Adult; Aged; Amyloid Neuropathies, Familial; Cohort Studies; Disease Progression; DNA Mutational Analysis; Female; Genes, Dominant; Humans; Male; Middle Aged; Mutation, Missense; Neural Conduction; Neurologic Examination; Peripheral Nervous System Diseases; Phenotype; Prealbumin; Retrospective Studies; Tyrosine | 2016 |
PARP inhibition attenuates neuroinflammation and oxidative stress in chronic constriction injury induced peripheral neuropathy.
Topics: Animals; Benzamides; Constriction, Pathologic; Cyclooxygenase 2; Hyperalgesia; Inflammation; Male; NAD; Neuritis; Neuroprotective Agents; Oxidative Stress; Pain Measurement; Peripheral Nervous System Diseases; Poly(ADP-ribose) Polymerase Inhibitors; Rats; Rats, Sprague-Dawley; Sensation; Tyrosine; Walking | 2016 |
A transthyretin mutation (Tyr78Phe) associated with peripheral neuropathy, carpal tunnel syndrome and skin amyloidosis.
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 |
Fyn kinase-mediated phosphorylation of NMDA receptor NR2B subunit at Tyr1472 is essential for maintenance of neuropathic pain.
Topics: Animals; Behavior, Animal; Blotting, Western; Dinoprostone; Dose-Response Relationship, Drug; Histocytochemistry; Mice; Mice, Inbred C57BL; Mice, Inbred CBA; Mice, Knockout; Microscopy, Immunoelectron; Neoplasm Proteins; Nitric Oxide; Pain; Peripheral Nervous System Diseases; Phosphorylation; Piperidines; Protein-Tyrosine Kinases; Receptors, N-Methyl-D-Aspartate; Signal Transduction; src-Family Kinases; Tyrosine | 2005 |
Optimization of the Y831C mutation detection in human DNA polymerase gamma by allelic discrimination assay.
Topics: Cysteine; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Gene Frequency; Genetic Techniques; Humans; Mitochondrial Diseases; Parkinson Disease; Peripheral Nervous System Diseases; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Tyrosine | 2006 |
Orthostatic hypotension in familial amyloid polyneuropathy: treatment with DL-threo-3,4-dihydroxyphenylserine.
Topics: Adult; Amyloidosis; Blood Pressure; Droxidopa; Female; Humans; Hypotension, Orthostatic; Male; Middle Aged; Norepinephrine; Peripheral Nervous System Diseases; Serine; Tyrosine | 1981 |
Neurological crisis in hereditary tyrosinaemia and complete reversal after liver transplantation.
Topics: Amino Acid Metabolism, Inborn Errors; Female; Humans; Infant; Liver Transplantation; Peripheral Nervous System Diseases; Phrenic Nerve; Tyrosine | 1994 |
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenase.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Amino Acid Metabolism, Inborn Errors; Child, Preschool; Cyclohexanones; Electromyography; Female; Humans; Neural Conduction; Nitrobenzoates; Peripheral Nervous System Diseases; Tyrosine | 1993 |
Neurologic crises in hereditary tyrosinemia.
Topics: Acute Disease; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Child, Preschool; Humans; Hypesthesia; Intestinal Pseudo-Obstruction; Muscle Hypertonia; Pain; Peripheral Nerves; Peripheral Nervous System Diseases; Self Mutilation; Tyrosine; Vomiting | 1990 |
A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases.
Topics: Adult; Amyloidosis; Base Sequence; Cysteine; DNA; Exons; Humans; Male; Molecular Sequence Data; Mutation; Peripheral Nervous System Diseases; Polymerase Chain Reaction; Prealbumin; Tyrosine | 1990 |