phenylalanine has been researched along with Motor Neuron Disease 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 | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benajiba, L; Brice, A; Campion, D; Camu, W; Camuzat, A; Couratier, P; Decousus, M; Dubois, B; Golfier, V; Guedj, E; Hannequin, D; Lacomblez, L; Lacoste, M; Le Ber, I; Legallic, S; Meininger, V; Salachas, F; Thomas-Anterion, C | 1 |
| Cindas, A; Ilgun, E; Koyuncuoglu, H; Soyupek, F; Tak, R | 1 |
| Barkats, M; Duque, S; Lambert, B; Maystadt, I; Munnich, A; Najimi, M; Remacle, S; Rezsöhazy, R; Sokal, E; Vannuffel, P; Verellen-Dumoulin, C; Viollet, L | 1 |
3 other study(ies) available for phenylalanine and Motor Neuron Disease
| Article | Year |
|---|---|
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration.
Topics: Adult; Aged; Dementia; DNA Mutational Analysis; DNA-Binding Proteins; Family Health; Female; Humans; Male; Middle Aged; Motor Neuron Disease; Mutation; Phenylalanine | 2009 |
The rehabilitation programme of an adult phenylketonuria with upper motor neuron involvement.
Topics: Botulinum Toxins, Type A; Combined Modality Therapy; Cryotherapy; Humans; Male; Motor Neuron Disease; Muscle Spasticity; Phenylalanine; Phenylketonurias; Vitamin B 12; Young Adult | 2009 |
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset.
Topics: Age of Onset; Amino Acid Sequence; Animals; Cells, Cultured; Child; Genes, Recessive; Guanine Nucleotide Exchange Factors; Humans; Mice; Molecular Sequence Data; Motor Neuron Disease; Mutation, Missense; NF-kappa B; Pedigree; Phenylalanine; Protein Conformation; Serine; Transfection | 2007 |