phenylalanine has been researched along with Benign Frontal Childhood Epilepsy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benjamin, C; Berkovic, SF; Fedi, M; Reutens, DC; Saling, MM; Scheffer, IE; Wood, AG | 1 |
| Caloustian, C; Cobo, AM; Galán, J; Grid, D; Jiménez, MD; López de Munain, A; Lorenzo, F; Márquez, C; Poza, JJ; Prud'homme, JF; Rodríguez, N; Sáenz, A | 1 |
2 other study(ies) available for phenylalanine and Benign Frontal Childhood Epilepsy
| Article | Year |
|---|---|
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy.
Topics: Adult; Association Learning; Circadian Rhythm; Cognition Disorders; Epilepsy, Frontal Lobe; Female; Frontal Lobe; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Middle Aged; Mutation; Neuropsychological Tests; Pedigree; Phenylalanine; Polysomnography; Receptors, Nicotinic; Serine; Young Adult | 2010 |
Autosomal dominant nocturnal frontal lobe epilepsy in a Spanish family with a Ser252Phe mutation in the CHRNA4 gene.
Topics: Adult; Alleles; Child; Child, Preschool; DNA Mutational Analysis; Electroencephalography; Epilepsy, Frontal Lobe; Female; Humans; Male; Middle Aged; Pedigree; Phenylalanine; Point Mutation; Receptors, Nicotinic; Serine; Spain | 1999 |