threonine has been researched along with Migraine with Aura 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 | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Annesi, G; Cestèle, S; Franceschetti, S; Gambardella, A; Labate, A; Mantegazza, M; Mumoli, L; Rusconi, R; Tarantino, P | 1 |
| Johnson, JE; Kanavakis, E; Leppert, MF; Ptacek, LJ; Schlesinger-Massart, MB; Silver, K; Swoboda, KJ; Xaidara, A; Youroukos, S | 1 |
| Beauvais, K; Cavé-Riant, F; De Barace, C; Furby, A; Tardieu, M; Tournier-Lasserve, E | 1 |
| Gargus, JJ; Tournay, A | 1 |
1 review(s) available for threonine and Migraine with Aura
| Article | Year |
|---|---|
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
Topics: Adolescent; Adult; Cell Line, Transformed; Computer Simulation; DNA Mutational Analysis; Electric Stimulation; Female; Humans; Italy; Male; Membrane Potentials; Middle Aged; Migraine with Aura; Models, Molecular; Mutation; NAV1.1 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Phenotype; Seizures; Serine; Threonine; Young Adult | 2013 |
3 other study(ies) available for threonine and Migraine with Aura
| Article | Year |
|---|---|
Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation.
Topics: Age of Onset; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Hemiplegia; Humans; Infant; Male; Migraine with Aura; Mutation; Pedigree; Phenotype; Sequence Alignment; Sodium-Potassium-Exchanging ATPase; Threonine | 2004 |
New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.
Topics: Adolescent; Calcium Channels; DNA Mutational Analysis; Female; Humans; Isoleucine; Migraine with Aura; Mutation; Status Epilepticus; Threonine | 2004 |
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3.
Topics: Adult; Child, Preschool; DNA Mutational Analysis; Family Health; Female; Humans; Male; Migraine with Aura; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Neurologic Examination; Seizures; Serine; Sodium Channels; Threonine | 2007 |