leucine has been researched along with Convulsions, Febrile in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chudley, AE; Hartley, JN; Mhanni, AA; Sanger, WG; Spriggs, EL | 1 |
| Archacki, S; Cui, X; Du, R; Liu, J; Liu, M; Liu, Y; Tang, Z; Wang, QK; Zeng, F; Zhan, T; Zhang, J | 1 |
| Arinami, T; Hamano, K; Iwasaki, N; Matsui, A; Nakahara, S; Nakayama, J; Ohta, M | 1 |
3 other study(ies) available for leucine and Convulsions, Febrile
| Article | Year |
|---|---|
Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder.
Topics: Child, Preschool; Epilepsy; Gene Expression Regulation; Genes, Dominant; Genetic Variation; Humans; Leucine; Male; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Pedigree; Seizures, Febrile; Sodium Channels; Valine | 2011 |
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 |
Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients.
Topics: Alleles; Brain; Case-Control Studies; DNA Mutational Analysis; Epilepsy, Temporal Lobe; Gene Expression; Genetic Predisposition to Disease; Genetic Variation; Humans; Intracellular Signaling Peptides and Proteins; Introns; Japan; Leucine; Point Mutation; Polymorphism, Genetic; Proteins; Seizures, Febrile | 2003 |