glutamine has been researched along with Atrophy, Muscular, Peroneal in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alberti, JM; Baloh, RH; Biris, N; Dorn, GW; Franco, A; Gavathiotis, E; Janetka, JW; Kitsis, RN; Knight, WC; Krezel, AM; Mochly-Rosen, D; Rocha, AG; Rumsey, JM; Townsend, RR; Zacharioudakis, E | 1 |
| Berciano, J; De Vriendt, E; Gallardo, E; García, A; Infante, J; Jordanova, A; Peeters, K; Pelayo-Negro, AL | 1 |
| Arnaud, E; Cartoni, R; Chrast, R; Courvoisier, DS; Martinou, JC; Médard, JJ; Poirot, O | 1 |
| Azzedine, H; Brice, A; Dubourg, O; Ente, D; Gilardeau, C; LeGuern, E; Périé, S; Ruberg, M; Wechsler, B | 1 |
| Inoue, H; Kanazawa, H; Matsushita, M; Nakamura, N; Tanaka, S | 1 |
| Baránková, L; Horácek, O; Hühne, K; Mazanec, R; Mikesová, E; Rautenstrauss, B; Seeman, P; Vyhnálek, M | 1 |
| Conforti, FL; Gabriele, AL; Gambardella, A; Magariello, A; Mazzei, R; Muglia, M; Patitucci, A; Quattrone, A; Rodolico, C; Toscano, A | 1 |
7 other study(ies) available for glutamine and Atrophy, Muscular, Peroneal
| Article | Year |
|---|---|
MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.
Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine | 2018 |
NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.
Topics: Action Potentials; Adult; Charcot-Marie-Tooth Disease; Creatine Kinase; DNA Mutational Analysis; Electrophysiology; Evoked Potentials; Family Health; Female; Follow-Up Studies; Glutamine; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neural Conduction; Neurofilament Proteins; Tomography, X-Ray Computed | 2015 |
Expression of mitofusin 2(R94Q) in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A.
Topics: Aging; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; DNA, Complementary; Glutamine; GTP Phosphohydrolases; Humans; Membrane Transport Proteins; Mice; Mice, Transgenic; Microscopy, Electron; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Mutation; Nerve Fibers, Myelinated; Neurons; Peripheral Nerves; Phenotype; Sciatic Nerve | 2010 |
Variability of disease progression in a family with autosomal recessive CMT associated with a S194X and new R310Q mutation in the GDAP1 gene.
Topics: Adult; Arginine; Charcot-Marie-Tooth Disease; Disease Progression; DNA Mutational Analysis; Electrophysiology; Family; Female; Genes, Recessive; Glutamine; Humans; Male; Mutation; Nerve Tissue Proteins; Pedigree; Phenotype; Serine | 2003 |
A novel kinesin-like protein, KIF1Bbeta3 is involved in the movement of lysosomes to the cell periphery in non-neuronal cells.
Topics: Animals; Antigens, CD; Base Sequence; Cell Nucleus; Charcot-Marie-Tooth Disease; Chlorocebus aethiops; Cloning, Molecular; COS Cells; Cytoplasm; Endosomes; Glutamine; Humans; Kidney; Kinesins; Lysosomal Membrane Proteins; Lysosomes; Molecular Motor Proteins; Molecular Sequence Data; Mutation; Nerve Tissue Proteins; Protein Isoforms; Protein Structure, Tertiary; Protein Transport; Rats; Sequence Alignment; Subcellular Fractions | 2004 |
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis.
Topics: Adolescent; Arginine; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; DNA-Binding Proteins; Female; Glutamine; Humans; Male; Mutation; Neural Conduction; Neurologic Examination; Peripheral Nerves; Radiography; Scoliosis; Trans-Activators; Transcriptional Regulator ERG | 2005 |
Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene.
Topics: Amino Acid Substitution; Arginine; Charcot-Marie-Tooth Disease; Glutamine; Humans; Male; Middle Aged; Molecular Sequence Data; Myelin P0 Protein; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational | 2000 |