arginine has been researched along with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kleopa, KA; Ong, J; Sutton, LN; Telfeian, AE; Tennekoon, G | 1 |
| Burns, TM; Dimberg, EL; Klein, CJ; Phillips, LH; Vaught, BK | 1 |
| Chiba, S; Hayasaka, K; Kasai, K; Naganuma, M; Tachi, N; Uyemura, K | 1 |
| Fujiki, K; Hayakawa, M; Hotta, Y; Kanai, A; Nakajima, A; Saito, K | 1 |
| Elsas, LJ; Hodge, JA; Lezza, AM; Lott, MT; Nikoskelainen, EK; Schurr, TG; Singh, G; Wallace, DC | 1 |
5 other study(ies) available for arginine and Charcot-Marie-Tooth Disease, Demyelinating, Type 4f
| Article | Year |
|---|---|
Conus medulla-cauda compression from nerve root hypertrophy in a child with Dejerine-Sottas syndrome: improvement with laminectomy and duraplasty. Case report.
Topics: Amino Acid Substitution; Arginine; Child; Codon; Decompression, Surgical; Glycine; Hereditary Sensory and Motor Neuropathy; Humans; Hypertrophy; Laminectomy; Magnetic Resonance Imaging; Male; Myelin P0 Protein; Neurologic Examination; Point Mutation; Polyradiculopathy; Postoperative Complications; Spinal Cord Compression; Spinal Nerve Roots | 2002 |
Novel myelin protein zero mutation (Arg36Trp) in a patient with acute onset painful neuropathy.
Topics: Acute Disease; Amino Acid Substitution; Arginine; Disease Progression; DNA Mutational Analysis; Genetic Predisposition to Disease; Genetic Testing; Hereditary Sensory and Motor Neuropathy; Humans; Inheritance Patterns; Male; Middle Aged; Myelin P0 Protein; Neuralgia; Peripheral Nerves; Peripheral Nervous System Diseases; Point Mutation; Polyradiculoneuropathy, Chronic Inflammatory Demyelinating; Time Factors; Tryptophan | 2006 |
Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III.
Topics: Adolescent; Arginine; Glycine; Hereditary Sensory and Motor Neuropathy; Humans; Immunoblotting; Immunohistochemistry; Male; Myelin P0 Protein; Myelin Proteins; Nerve Fibers, Myelinated; Nerve Tissue Proteins; Point Mutation; RNA, Messenger; Sural Nerve | 1994 |
Diagnosis of Leber's optic neuropathy by means of polymerase chain reaction amplification.
Topics: Adult; Arginine; DNA Mutational Analysis; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Gene Amplification; Hereditary Sensory and Motor Neuropathy; Histidine; Humans; Male; Optic Atrophies, Hereditary; Pedigree; Polymerase Chain Reaction; Visual Acuity | 1989 |
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Topics: Animals; Arginine; Black People; Cytochrome Reductases; DNA, Mitochondrial; Female; Genes; Georgia; Hereditary Sensory and Motor Neuropathy; Histidine; Humans; Macromolecular Substances; Male; Mutation; NADH Dehydrogenase; Optic Atrophies, Hereditary; Pedigree; Reference Values; White People | 1988 |