Compounds > arginine

arginine and Muscle Weakness

arginine has been researched along with Muscle Weakness in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (7.69)18.2507
2000's7 (53.85)29.6817
2010's4 (30.77)24.3611
2020's1 (7.69)2.80

Authors

AuthorsStudies
Furey, A; Liu, M; Rahman, P; Randell, EW; Sun, G; Werdyani, S; Zhai, G; Zhang, H1
Arnold, P; Bautmans, I; Buyl, R; Gorus, E; Njemini, R; Pool-Goudzwaard, A; Vantieghem, S1
Bisceglie, L; Braren, R; Gehrig, P; Hopp, AK; Hottiger, MO; Koch-Nolte, F; Leutert, M; Li, H; Menzel, S; Nowak, K; Rissiek, B; Zolkiewska, A1
Hashiguchi, A; Higuchi, I; Higuchi, Y; Nozuma, S; Okamoto, Y; Sakiyama, Y; Takashima, H; Yoshimura, A; Yuan, J1
Barisic, I; Drmic, D; Katancic, J; Kolenc, D; Medvidovic-Grubisic, M; Murselovic, T; Plestina-Borjan, I; Seiwerth, S; Sikiric, P; Sindic, A; Stambolija, V; Strbe, S1
Mayles, WJ; Sandoval, PA; Weitzel, LR; Wischmeyer, PE1
Durling, HJ; Gunning, P; Laing, NG; Lochmüller, H; Mendel, B; Müller-Höcker, J; Pongratz, D; Reilich, P; Wallgren-Pettersson, C1
Benedetti, S; Bertini, E; Bonne, G; D'Amico, A; Ferreiro, A; Guicheney, P; Haliloglu, G; Maugenre, S; Menditto, I; Richard, P; Talim, B; Topaloglu, H1
Fidziańska, A; Goudeau, B; Hausmanowa-Petrusewicz, I; Kotowicz, J; Sadowska, M; Vicart, P; Walczak, E1
Holmgren, D; Kimber, E; Oldfors, A; Tajsharghi, H; Tulinius, M1
Dubowitz, V; Lehmann-Horn, F; Lerche, H; Mitrovic, N1
Corbett, MA; Dunglison, GF; Gunning, PW; Hardeman, EC; Joya, JE; North, KN; Robinson, CS; Schnell, C; Stewart, AW; Yang, N1
Adachi, Y; Kumada, H; Kusumi, M; Nakashima, K1

Reviews

1 review(s) available for arginine and Muscle Weakness

ArticleYear
Performance-enhancing sports supplements: role in critical care.
    Critical care medicine, 2009, Volume: 37, Issue:10 Suppl

    Topics: Amino Acids, Branched-Chain; Anabolic Agents; Androgens; Arginine; Creatine; Critical Care; Critical Illness; Dietary Supplements; Glutamine; Human Growth Hormone; Humans; Intensive Care Units; Muscle Weakness; Muscle, Skeletal; Testosterone

2009

Other Studies

12 other study(ies) available for arginine and Muscle Weakness

ArticleYear
Endotypes of primary osteoarthritis identified by plasma metabolomics analysis.
    Rheumatology (Oxford, England), 2021, 06-18, Volume: 60, Issue:6

    Topics: Aged; Arginine; Body Mass Index; Carnitine; Case-Control Studies; Coronary Disease; Diabetes Mellitus; Factor Analysis, Statistical; Fasting; Female; Humans; Logistic Models; Lysophosphatidylcholines; Male; Metabolomics; Muscle Weakness; Osteoarthritis, Hip; Osteoarthritis, Knee; Osteoporosis; Palmitic Acid; Prevalence; Quality Control; Wasting Syndrome

2021
Reaction time in healthy elderly is associated with chronic low-grade inflammation and advanced glycation end product.
    Experimental gerontology, 2018, 07-15, Volume: 108

    Topics: Aged; Aged, 80 and over; Aging; Arginine; Biomarkers; Electromyography; Female; Glycation End Products, Advanced; Humans; Inflammation; Isometric Contraction; Linear Models; Lysine; Male; Muscle Weakness; Muscle, Skeletal; Reaction Time; Sarcopenia; Sex Factors

2018
Proteomic Characterization of the Heart and Skeletal Muscle Reveals Widespread Arginine ADP-Ribosylation by the ARTC1 Ectoenzyme.
    Cell reports, 2018, 08-14, Volume: 24, Issue:7

    Topics: ADP Ribose Transferases; ADP-Ribosylation; Animals; Arginine; Carrier Proteins; Cell Line; Gene Ontology; Heme; Hemopexin; Isoenzymes; Male; Membrane Proteins; Mice; Mice, Knockout; Molecular Sequence Annotation; Muscle Fibers, Skeletal; Muscle Proteins; Muscle Weakness; Muscle, Skeletal; Myocardium; Protein Binding; Protein Processing, Post-Translational; Proteome; Proteomics; Signal Transduction

2018
Clinical and Electron Microscopic Findings in Two Patients with Mitochondrial Myopathy Associated with Episodic Hyper-creatine Kinase-emia.
    Internal medicine (Tokyo, Japan), 2015, Volume: 54, Issue:24

    Topics: Adult; Aged; Arginine; Creatine Kinase; Electrons; Female; Humans; Male; Mitochondria; Mitochondrial Myopathies; Muscle Weakness; Myalgia

2015
Hypermagnesemia disturbances in rats, NO-related: pentadecapeptide BPC 157 abrogates, L-NAME and L-arginine worsen.
    Inflammopharmacology, 2017, Volume: 25, Issue:4

    Topics: Amino Acid Sequence; Animals; Anti-Ulcer Agents; Arginine; Drug Therapy, Combination; Enzyme Inhibitors; HEK293 Cells; Humans; Magnesium Sulfate; Male; Muscle Weakness; NG-Nitroarginine Methyl Ester; Nitric Oxide; Peptide Fragments; Proteins; Rats; Rats, Wistar

2017
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy.
    Neuromuscular disorders : NMD, 2002, Volume: 12, Issue:10

    Topics: Adenosine Triphosphatases; Adolescent; Arginine; DNA Mutational Analysis; Drosophila Proteins; Exons; Female; Genetic Carrier Screening; Histidine; Humans; Muscle Fibers, Skeletal; Muscle Weakness; Mutation, Missense; Myopathies, Nemaline; Tropomyosin

2002
Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:8

    Topics: Arginine; Child; DNA Mutational Analysis; Female; Glycine; Humans; Infant; Lamin Type A; Lamins; Male; Muscle Proteins; Muscle Weakness; Muscular Dystrophies; Mutation; Neck Muscles; Selenoproteins; Syndrome

2005
A novel desmin R355P mutation causes cardiac and skeletal myopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:8

    Topics: Adult; alpha-Crystallin B Chain; Arginine; Desmin; DNA Mutational Analysis; Humans; Immunohistochemistry; Intermediate Filament Proteins; Male; Microscopy, Electron, Transmission; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Nerve Tissue Proteins; Proline; Protein Kinases; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

2005
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation.
    Neurology, 2007, Mar-06, Volume: 68, Issue:10

    Topics: Adult; Aged; Arginine; Arthrogryposis; DNA Mutational Analysis; Exons; Family Health; Female; Humans; Muscle Weakness; Mutation, Missense; Tropomyosin; Tryptophan

2007
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle.
    Annals of neurology, 1996, Volume: 39, Issue:5

    Topics: Adult; Arginine; Biopsy; Cold Temperature; Female; Hot Temperature; Humans; Ion Channel Gating; Isometric Contraction; Microelectrodes; Muscle Weakness; Muscle, Skeletal; Myotonia Congenita; Patch-Clamp Techniques; Point Mutation; Proline; Sodium Channels; Walking

1996
A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy.
    Human molecular genetics, 2001, Feb-15, Volume: 10, Issue:4

    Topics: Amino Acid Substitution; Animals; Arginine; Disease Models, Animal; Dissection; Female; Glycolysis; Humans; Hypertrophy; Inclusion Bodies; Methionine; Mice; Mice, Inbred Strains; Mice, Transgenic; Microtubules; Muscle Development; Muscle Fibers, Fast-Twitch; Muscle Fibers, Slow-Twitch; Muscle Weakness; Muscle, Skeletal; Myopathies, Nemaline; Oxidation-Reduction; Point Mutation; RNA, Messenger; Sarcoplasmic Reticulum; Strontium; Tropomyosin

2001
Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis.
    Psychiatry and clinical neurosciences, 2001, Volume: 55, Issue:5

    Topics: Adult; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Child; Codon; Female; Histidine; Humans; Hypokalemic Periodic Paralysis; Male; Muscle Weakness; Pedigree; Point Mutation

2001