arginine has been researched along with Cryptogenic Infantile Spasms 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 | 0 (0.00) | 29.6817 |
| 2010's | 4 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aoto, K; Belal, H; Kato, M; Kumada, S; Leong, HY; Lerman-Sagie, T; Lev, D; Matsumoto, N; Miyake, N; Miyatake, S; Mizuguchi, T; Mukaida, S; Nakashima, M; Ogata, K; Saitsu, H; Sato, A; Shiina, M; Tsurusaki, Y; Zerem, A | 1 |
| Ramakrishnaiah, R; Samanta, D | 1 |
| Ambrosino, P; Cooper, EC; De Maria, M; Joshi, N; Keator, C; Miceli, F; Mikati, MA; Millichap, JJ; Shashi, V; Soldovieri, MV; Taglialatela, M; Tran, B | 1 |
| Ben-Zeev, B; Carroll, JL; Cilio, MR; Cooper, EC; Grønborg, S; Jiang, YH; Joshi, N; Kelly, M; Koolen, DA; Mikati, MA; Mulkey, SB; Nicolai, J; Park, K; Pearl, PL; Scheffer, IE; Spillmann, RC; Taglialatela, M; Vieker, S; Weckhuysen, S | 1 |
4 other study(ies) available for arginine and Cryptogenic Infantile Spasms
| Article | Year |
|---|---|
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathy.
Topics: Adaptor Proteins, Signal Transducing; Animals; Arginine; Brain; Cell Line, Transformed; Child; Child, Preschool; Electroencephalography; Exome Sequencing; Female; Gene Expression Regulation, Developmental; Green Fluorescent Proteins; HEK293 Cells; Humans; Infant; Magnetic Resonance Imaging; Male; Mice; Models, Molecular; Mutation; Pedigree; Spasms, Infantile; Transfection | 2018 |
De novo R853Q mutation of SCN2A gene and West syndrome.
Topics: Arginine; Glutamine; Humans; Infant; Male; Mutation; NAV1.2 Voltage-Gated Sodium Channel; Spasms, Infantile | 2015 |
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant.
Topics: Animals; Arginine; Brain Diseases; Cells, Cultured; Child; Child, Preschool; CHO Cells; Cricetulus; Glutamine; Hippocampus; Humans; Infant; KCNQ2 Potassium Channel; Longitudinal Studies; Membrane Potentials; Models, Molecular; Mutation; Neurons; Rats; Spasms, Infantile; Transfection | 2017 |
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.
Topics: Anticonvulsants; Arginine; Child, Preschool; Cysteine; Electroencephalography; Female; Histidine; Humans; Infant; Infant, Newborn; KCNQ2 Potassium Channel; Magnetic Resonance Imaging; Male; Myoclonus; Phenotype; Polymorphism, Single Nucleotide; Registries; Respiration Disorders; Spasms, Infantile | 2017 |