glutamine has been researched along with Spasms, Infantile in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (80.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haginoya, K; Iinuma, K; Kobayashi, Y; Kure, S; Munakata, M; Onuma, A; Sakamoto, O; Togashi, N | 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 |
| Accorsi, P; Bernardina, BD; Bettella, E; Darra, F; Galli, J; Giordano, L; Marchi, M; Murgia, A; Russo, S; Sartori, S; Tiberti, A; Vignoli, A | 1 |
| FARINA, M; RENSON, L | 1 |
5 other study(ies) available for glutamine and Spasms, Infantile
| Article | Year |
|---|---|
Reduction in glutamine/glutamate levels in the cerebral cortex after adrenocorticotropic hormone therapy in patients with west syndrome.
Topics: Adrenocorticotropic Hormone; Aspartic Acid; Choline; Cosyntropin; Electroencephalography; Female; Glutamic Acid; Glutamine; Humans; Infant; Inositol; Magnetic Resonance Spectroscopy; Male; Occipital Lobe; Spasms, Infantile | 2014 |
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 |
Familial Ohtahara syndrome due to a novel ARX gene mutation.
Topics: Base Sequence; Epilepsy; Exons; Family; Female; Genes, Homeobox; Glutamine; Homeodomain Proteins; Humans; Infant, Newborn; Male; Mutation; Pedigree; Phenotype; Spasms, Infantile; Syndrome; Transcription Factors | 2010 |
[Preliminary note apropos of a new possibility of therapy of infantile myoclonic encephalopathy with hypsarrhythmia].
Topics: Child; Electroencephalography; Encephalitis; Epilepsies, Myoclonic; Glutamine; Humans; Infant; Myoclonus; Seizures; Spasms, Infantile | 1961 |