leucine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia 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 |
|---|---|
| Burness, CE; Chinnery, PF; Cox, LE; Dalton, A; Hadjivassiliou, M; Hewamadduma, C; Kirby, J; McDermott, CJ; Rao, DG; Sharrack, B; Shaw, PJ | 1 |
| Bertelli, M; Buda, A; Cecchin, S; Fabbri, A; Lapucci, C; Lorusso, L; Pandolfo, M; Sidoti, V | 1 |
| Cho, HJ; Ki, CS; Sung, DH | 1 |
3 other study(ies) available for leucine and Autosomal Dominant Hereditary Spastic Paraplegia
| Article | Year |
|---|---|
Clinical features of hereditary spastic paraplegia due to spastin mutation.
Topics: Adenosine Triphosphatases; Adult; Aged; Cohort Studies; DNA Mutational Analysis; Exons; Female; Genetic Testing; Glutamine; Humans; Leucine; Male; Middle Aged; Mutation; Phenotype; Proline; Retrospective Studies; Serine; Spastic Paraplegia, Hereditary; Spastin; United Kingdom | 2006 |
Identification of a novel mutation in the spastin gene (SPG4) in an Italian family with hereditary spastic paresis.
Topics: Adenosine Triphosphatases; Adult; Aged; Cytosine; Exons; Female; Genes, Dominant; Humans; Italy; Leucine; Magnetic Resonance Imaging; Male; Mutation, Missense; Proline; Spastic Paraplegia, Hereditary; Spastin; Thymine | 2006 |
Identification of de novo BSCL2 Ser90Leu mutation in a Korean family with Silver syndrome and distal hereditary motor neuropathy.
Topics: Adolescent; Adult; Amino Acid Substitution; DNA Mutational Analysis; Female; GTP-Binding Protein gamma Subunits; Humans; Korea; Leucine; Male; Mutation, Missense; Pedigree; Reflex, Babinski; Serine; Spastic Paraplegia, Hereditary; Syndrome | 2007 |