phenylalanine has been researched along with Convulsive Generalized Seizure Disorder in 2 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 | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Archacki, S; Cui, X; Du, R; Liu, J; Liu, M; Liu, Y; Tang, Z; Wang, QK; Zeng, F; Zhan, T; Zhang, J | 1 |
| Hosoki, K; Saitoh, S; Sudo, A; Takeichi, N | 1 |
2 other study(ies) available for phenylalanine and Convulsive Generalized Seizure Disorder
| Article | Year |
|---|---|
A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
Topics: Adolescent; Adult; Aged; Asian People; Child; Child, Preschool; DNA Mutational Analysis; Epilepsy, Generalized; Family Health; Female; Genetic Linkage; Genetic Predisposition to Disease; Humans; Leucine; Male; Middle Aged; Models, Molecular; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Phenylalanine; Seizures, Febrile; Sodium Channels | 2011 |
Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition.
Topics: Audiometry, Pure-Tone; Brain; Child; Cochlear Implantation; Electron Transport Complex III; Epilepsy, Generalized; Female; Genome, Mitochondrial; Growth Disorders; Hearing Loss, Sensorineural; Humans; Hypertrichosis; Lactates; Magnetic Resonance Imaging; Mitochondria; Mitochondrial Diseases; Phenylalanine; Point Mutation; RNA, Transfer; Treatment Outcome | 2011 |