cysteine has been researched along with Hemiplegia in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 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 | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andersen, JP; Artigas, P; Einholm, AP; Holm, R; Khandelwal, J; Vilsen, B | 1 |
Alonso, I; Barros, J; Coelho, J; Coutinho, P; Sequeiros, J; Silveira, I; Tuna, A | 1 |
Hamano, S; Hayakawa, M; Minamitani, M; Tanaka, M; Yamashita, S; Yoshinari, S | 1 |
Abroms, IF; Carney, M; Cloherty, JP; Johnson, JL; Mandell, R; Rajagopalan, KV; Robb, RM; Shih, VE | 1 |
4 other study(ies) available for cysteine and Hemiplegia
Article | Year |
---|---|
Arginine substitution of a cysteine in transmembrane helix M8 converts Na+,K+-ATPase to an electroneutral pump similar to H+,K+-ATPase.
Topics: Amino Acid Substitution; Arginine; Binding Sites; Binding, Competitive; Cations; Cell Membrane; Cysteine; H(+)-K(+)-Exchanging ATPase; Hemiplegia; Humans; Ion Channels; Ion Transport; Models, Molecular; Mutagenesis, Site-Directed; Phenylalanine; Potassium; Protein Conformation; Protein Subunits; Proton Pumps; Sequence Alignment; Sodium; Sodium-Potassium-Exchanging ATPase | 2017 |
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Topics: Adolescent; Adult; Alanine; Child; Cysteine; Female; Genetic Linkage; Glycine; Hemiplegia; Humans; Lod Score; Male; Microsatellite Repeats; Middle Aged; Migraine Disorders; Mutation, Missense; Phenotype; Polymorphism, Single-Stranded Conformational; Spinocerebellar Ataxias | 2003 |
[Single photon emission computed tomography findings in a case of alternating hemiplegia of childhood in relation to migraine].
Topics: Atrophy; Cerebellum; Child; Cysteine; Electroencephalography; Hemiplegia; Humans; Iodine Radioisotopes; Iofetamine; Magnetic Resonance Imaging; Male; Migraine Disorders; Organotechnetium Compounds; Radiopharmaceuticals; Tomography, Emission-Computed, Single-Photon | 2005 |
Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism.
Topics: Amino Acids, Sulfur; Child, Preschool; Cysteine; Hemiplegia; Humans; Lens Subluxation; Male; Metabolism, Inborn Errors; Methionine; Oxidoreductases; Sulfites; Sulfur | 1977 |