proline has been researched along with Spastic Paraplegia, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 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 |
| Chitayat, D; Fransen, E; Holden, JJ; Van Camp, G; Vits, L; Willems, PJ | 1 |
3 other study(ies) available for proline and Spastic Paraplegia, Hereditary
| 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 |
Evidence for somatic and germline mosaicism in CRASH syndrome.
Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Amino Acid Substitution; Arginine; DNA; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; Germ-Line Mutation; Humans; Hydrocephalus; Intellectual Disability; Leukocyte L1 Antigen Complex; Male; Membrane Glycoproteins; Mosaicism; Mutation; Neural Cell Adhesion Molecules; Pedigree; Polymorphism, Single-Stranded Conformational; Proline; Spastic Paraplegia, Hereditary; Thumb; X Chromosome | 1998 |