leucine has been researched along with Peripheral Nervous System Diseases in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (37.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bönnemann, C; Brockmann, K; Gärtner, J; Huebner, A; Kind, B; Koehler, K; Krumbholz, M | 1 |
| Chun, J; Nagai, J; Uchida, H; Ueda, H; Ueda, M; Xie, W | 1 |
| Rajabally, YA; Simpson, BS | 1 |
| Baracca, A; Carelli, V; Casalena, G; Lenaz, G; Mattiazzi, M; Moggio, M; Pagnotta, E; Sgarbi, G; Solaini, G; Valentino, ML | 1 |
| Ghandour, K; Krajewski, KM; Li, J; Nicholson, GA; Radovanovic, D; Shy, ME; Shy, RR | 1 |
| Baughman, S; Colip, MP; Peterson, RG | 1 |
| Baker, TS; Bus, JS; Gillies, PJ; Norton, RM | 1 |
| Donoso, JA; Green, LS; Heller-Bettinger, IE; Samson, FE | 1 |
8 other study(ies) available for leucine and Peripheral Nervous System Diseases
| Article | Year |
|---|---|
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.
Topics: Amino Acid Substitution; DNA Mutational Analysis; Female; HeLa Cells; Humans; Lacrimal Apparatus Diseases; Leucine; Muscular Atrophy; Musculoskeletal Abnormalities; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Peripheral Nervous System Diseases; Phenylalanine; Point Mutation; Syndrome; Transfection | 2008 |
Calpain-mediated down-regulation of myelin-associated glycoprotein in lysophosphatidic acid-induced neuropathic pain.
Topics: Animals; Calpain; Cysteine Proteinase Inhibitors; Demyelinating Diseases; Disease Models, Animal; Enzyme Activation; Leucine; Lysophospholipids; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Myelin-Associated Glycoprotein; Neurotoxins; Peripheral Nervous System Diseases; Receptors, Lysophosphatidic Acid; Sciatic Neuropathy; Sensory Receptor Cells; Spinal Nerve Roots | 2010 |
Charcot-Marie-Tooth disease due to novel myelin protein zero mutation presenting as late-onset remitting sensory neuropathy.
Topics: Adult; Charcot-Marie-Tooth Disease; Genetic Testing; Humans; Leucine; Male; Mutation; Myelin P0 Protein; Neurologic Examination; Peripheral Nervous System Diseases | 2010 |
Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993.
Topics: Adenosine Triphosphate; Adult; Ataxia; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genes, Mitochondrial; Humans; Leigh Disease; Leucine; Lymphocytes; Membrane Potentials; Middle Aged; Mitochondrial Proton-Translocating ATPases; Mutation; Peripheral Nervous System Diseases; Phenotype; Reactive Oxygen Species; Retinitis Pigmentosa | 2007 |
Stoichiometric alteration of PMP22 protein determines the phenotype of hereditary neuropathy with liability to pressure palsies.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; DNA Mutational Analysis; Down-Regulation; Electrodiagnosis; Female; Frameshift Mutation; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Heredodegenerative Disorders, Nervous System; Humans; Leucine; Male; Middle Aged; Myelin Proteins; Neural Conduction; Peripheral Nerves; Peripheral Nervous System Diseases; Phenotype | 2007 |
Alteration of fucose/leucine incorporation into PNS myelin by isoniazid neuropathy.
Topics: Animals; Fucose; Isoniazid; Leucine; Male; Myelin Proteins; Peripheral Nervous System Diseases; Rats; Sciatic Nerve; Tibial Nerve; Wallerian Degeneration | 1981 |
Altered lipid metabolism in 2,5-hexanedione-induced testicular atrophy and peripheral neuropathy in the rat.
Topics: Acetates; Animals; Atrophy; Hexanones; Ketones; Leucine; Lipid Metabolism; Liver; Male; Peripheral Nervous System Diseases; Rats; Sciatic Nerve; Testicular Diseases | 1981 |
Axonal transport disturbances in the vincristine-induced peripheral neuropathy.
Topics: Animals; Axonal Transport; Cats; Leucine; Peripheral Nervous System Diseases; Vincristine | 1975 |