Compounds > arginine

arginine and Abnormal Deep Tendon Reflex

arginine has been researched along with Abnormal Deep Tendon Reflex in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antal, M; Contreras, GA; Dormann, D; Fekecs, Z; Guo, X; Hickman, J; Hortobagyi, T; Horvath, A; Jiang, LL; Karolyi, K; Keresztessy, Z; Kiss, G; Kolostyak, Z; Nagy, L; Nógrádi, A; Pajer, K; Pap, A; Papp, Z; Patsalos, A; Reho, B; Sari, Z; Sieler, T; Simandi, Z; Vámosi, G; Xu, H1
Clarkson, KB; Edgar, TS; Gregory, ML; Guzauskas, GF; Holden, KR; Srivastava, AK1
Alvarez, V; Argente, J; Armenta, D; Castro, MG; Coto, E; Espinosa, R1
Rice, AS1

Other Studies

4 other study(ies) available for arginine and Abnormal Deep Tendon Reflex

ArticleYear
Arginine Methyltransferase PRMT8 Provides Cellular Stress Tolerance in Aging Motoneurons.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018, 08-29, Volume: 38, Issue:35

    Topics: Aging; Amino Acid Sequence; Animals; Arginine; Cell Line; Cyclic AMP Response Element-Binding Protein; DNA Breaks, Double-Stranded; DNA Damage; DNA Repair; Isometric Contraction; Male; Mice; Mice, Knockout; Mice, Transgenic; Motor Neurons; Muscle Cells; Neuromuscular Junction; Protein-Arginine N-Methyltransferases; Recombinant Fusion Proteins; Reflex, Abnormal; RNA Interference; RNA, Small Interfering; Rotarod Performance Test; Spinal Cord

2018
A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
    Journal of child neurology, 2008, Volume: 23, Issue:12

    Topics: Adult; Arginine; Black or African American; Child; Child, Preschool; Chromosomes, Human, Pair 5; DNA Mutational Analysis; Family Health; Female; Humans; Male; Middle Aged; Muscle Hypertonia; Mutation; Phenotype; Proline; Receptors, Glycine; Reflex, Abnormal

2008
Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene.
    Movement disorders : official journal of the Movement Disorder Society, 2005, Volume: 20, Issue:12

    Topics: Adolescent; Arginine; DNA Mutational Analysis; Family Health; Female; Histidine; Humans; Male; Mutation; Receptors, Glycine; Reflex, Abnormal

2005
Topical spinal administration of a nitric oxide synthase inhibitor prevents the hyper-reflexia associated with a rat model of persistent visceral pain.
    Neuroscience letters, 1995, Mar-03, Volume: 187, Issue:2

    Topics: Amino Acid Oxidoreductases; Analgesics; Anilides; Animals; Arginine; Cystitis; Female; Injections, Spinal; Nitric Oxide Synthase; Pain; Rats; Rats, Wistar; Reflex; Reflex, Abnormal; Turpentine; Urinary Bladder; Viscera

1995