cysteine has been researched along with Decreased Muscle Tone in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andrade, J; Neel, BG; Ueberheide, B; Xu, Y | 1 |
Agaimy, A; Berney, DM; Bonert, M; Brimo, F; Compérat, E; Frizzell, N; Gill, AJ; Hartmann, A; Hes, O; Hills, K; Husain, A; Kristiansen, G; Lüders, C; Maclean, F; Magi-Galluzzi, C; Martinek, P; Mehra, R; Nesi, G; Sibony, M; Srinivasan, B; Trpkov, K | 1 |
Goto, M; Ito, K; Okamoto, N; Sasaki, M; Sato, N | 1 |
Crofton, PM; Dean, JC; Hobson, EE; Lloyd, D; Murray, AD; Thomas, S | 1 |
4 other study(ies) available for cysteine and Decreased Muscle Tone
Article | Year |
---|---|
Activated Thiol Sepharose-based proteomic approach to quantify reversible protein oxidation.
Topics: Animals; Carrier Proteins; Cells, Cultured; Cysteine; Dimethyl Fumarate; Fumarate Hydratase; Membrane Proteins; Metabolism, Inborn Errors; Muscle Hypotonia; Oxidation-Reduction; Proteins; Proteomics; Psychomotor Disorders; Rats; Sepharose; Thyroid Hormone-Binding Proteins; Thyroid Hormones | 2019 |
Fumarate Hydratase-deficient Renal Cell Carcinoma Is Strongly Correlated With Fumarate Hydratase Mutation and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome.
Topics: Adult; Aged; Carcinoma, Renal Cell; Cysteine; Female; Fumarate Hydratase; Germ-Line Mutation; Humans; Immunohistochemistry; Kidney Neoplasms; Leiomyomatosis; Male; Metabolism, Inborn Errors; Middle Aged; Muscle Hypotonia; Neoplastic Syndromes, Hereditary; Psychomotor Disorders; Skin Neoplasms; Tissue Array Analysis; Uterine Neoplasms; Young Adult | 2016 |
Cerebral blood flow on (99m)Tc ethyl cysteinate dimer SPECT in 2 siblings with monocarboxylate transporter 8 deficiency.
Topics: Cerebrovascular Circulation; Child, Preschool; Cysteine; Humans; Infant; Magnetic Resonance Imaging; Male; Mental Retardation, X-Linked; Muscle Hypotonia; Muscular Atrophy; Organotechnetium Compounds; Regional Blood Flow; Siblings; Tomography, Emission-Computed, Single-Photon; Tomography, X-Ray Computed | 2013 |
Isolated sulphite oxidase deficiency mimics the features of hypoxic ischaemic encephalopathy.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Cysteine; Diagnosis, Differential; Fatal Outcome; Female; Humans; Hypoxia-Ischemia, Brain; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors; Muscle Hypotonia; Seizures; Siblings; Sulfite Oxidase | 2005 |