ornithine has been researched along with Spastic Paraplegia, Hereditary in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 4 (80.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bertini, E; Di Capua, M; Diodato, D; Dionisi-Vici, C; Longo, D; Martinelli, D; Olivieri, G; Pro, S | 1 |
| Alonso, I; Brice, A; Calvas, P; Charles, P; Coutelier, M; Coutinho, P; Darios, F; Depienne, C; Dionne-Laporte, A; Durand, CM; Durr, A; Gaussen, M; Goizet, C; Habarou, F; Jacoupy, M; Janin, M; Kennerson, M; Konop, J; Loureiro, JL; Mairey, M; Matusiak, R; Mochel, F; Morais, S; Morice-Picard, F; Nicholson, G; Ottolenghi, C; Rouleau, G; Saudubray, JM; Schule, R; Stevanin, G; Stoll, M; Tallaksen, C; Tao, F; Zuchner, S | 1 |
| Coutelier, M; Mochel, F; Ottolenghi, C; Saudubray, JM; Stevanin, G | 1 |
| Bordo, D; Cusano, R; Davies, S; De Michele, G; Donati, MA; Escamilla-Honrubia, JM; Gougeard, N; Hurst, JA; Liguori, R; Marco-Marín, C; Morra, VB; Németh, AH; Panza, E; Pippucci, T; Ravazzolo, R; Rubio, V; Salviati, L; Seri, M; Smithson, S | 1 |
| Dlouhy, SR; Geraghty, MT; Hodes, ME; Naidu, S | 1 |
5 other study(ies) available for ornithine and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia.
Topics: Adolescent; Adult; Brain; Child; Female; Humans; Hyperammonemia; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neural Conduction; Ornithine; Spastic Paraplegia, Hereditary; Spinal Cord; Urea Cycle Disorders, Inborn; Young Adult | 2019 |
Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia.
Topics: Adolescent; Adult; Aldehyde Dehydrogenase; Arginine; Female; Glutamic Acid; Humans; Male; Middle Aged; Mutation; Ornithine; Pedigree; Phenotype; Spastic Paraplegia, Hereditary; Young Adult | 2015 |
Reply: ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
Topics: Aldehyde Dehydrogenase; Female; Humans; Male; Mutation; Ornithine; Spastic Paraplegia, Hereditary | 2016 |
ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
Topics: Aldehyde Dehydrogenase; Female; Humans; Male; Mutation; Ornithine; Spastic Paraplegia, Hereditary | 2016 |
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.
Topics: Brain; Child, Preschool; Deoxyribonucleases, Type II Site-Specific; Diffuse Cerebral Sclerosis of Schilder; DNA; Genetic Linkage; Humans; Kidney; Lysine; Magnetic Resonance Imaging; Male; Mutation; Myelin Proteolipid Protein; Ornithine; Pedigree; Spastic Paraplegia, Hereditary; X Chromosome | 1997 |