nad has been researched along with Muscular Diseases in 32 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 19 (59.38) | 18.7374 |
1990's | 2 (6.25) | 18.2507 |
2000's | 3 (9.38) | 29.6817 |
2010's | 5 (15.63) | 24.3611 |
2020's | 3 (9.38) | 2.80 |
Authors | Studies |
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Brotto, M; Manickam, R; Tipparaju, SM; Wagner, S | 1 |
Cao, J; Ertbjerg, P; He, J; Pan, D; Wang, H; Wang, Y; Yang, Y | 1 |
Cardoso, D; Muchir, A | 1 |
Goody, MF; Henry, CA | 1 |
Al-Ajmi, A; Alefasi, SA; Aljeryan, LA; Alrashidi, NH; Alrohaif, H; Bastaki, L; Lochmüller, H; Pogoryelova, O; Urtizberea, A | 1 |
Bello, L; Bertolin, C; Calore, C; Catapano, F; Cenacchi, G; Colombo, I; Gavassini, BF; Guidolin, F; Minervini, G; Moggio, M; Pantic, B; Papa, V; Pegoraro, E; Previtero, M; Semplicini, C; Sorarù, G; Stramare, R; Tosatto, SCE; Vianello, S | 1 |
Hanson, MG; Minic, AD; Moreno, RL; Niswander, L; Wilde, JJ | 1 |
Amacher, DE; Ballinger, WE; Boldt, SE; Francone, OL; Kerlin, RL; Pettersen, JC; Pruimboom-Brees, I | 1 |
Clemen, CS; Eggermann, T; Fischer, D; Fürst, DO; Goudeau, B; Kunz, WS; Li, Z; Reimann, J; Rudnik-Schöneborn, S; Schröder, R; Simon, MC; van der Ven, PF; Vicart, P; Xue, Z; Zerres, K | 1 |
GONATAS, NK; SHY, GM | 1 |
EVANGELISTA, I; GONATAS, NK; PEREZ, MC; SHY, GM | 1 |
Andersen, PM; Brännström, T; Eisen, A; Mackenzie, IR; Marklund, SL; Stewart, HG | 1 |
Fukunaga, H; Igata, A; Osame, M | 1 |
Clark, JB; Hayes, DJ; Landon, DN; Morgan-Hughes, JA; Rudge, P; Stark, RJ; Swash, M | 1 |
Butler-Browne, GS; Hägg, G; Håkansson, R; Holmner, S; Kadi, F; Thornell, LE | 1 |
Ahlgren, C; Butler-Browne, GS; Holmner, S; Kadi, F; Sundelin, G; Thornell, LE; Waling, K | 1 |
Modi, G | 1 |
Duncan, ID; Griffiths, IR; McQueen, A | 1 |
Morales, RC; Rezzonico, C; Sfaello, ZM; Taratuto, AL | 1 |
Argov, Z; Bank, WJ; Berkowitz, HD; Boden, B; Buist, NM; Chance, B; Donlon, E; Kelley, R; McCully, K; Younkin, DP | 1 |
Hotta, Y; Kobayashi, M; Morishita, H; Nakano, M; Nonaka, I; Sugiyama, N; Terauchi, A; Wada, Y; Yokochi, K | 1 |
Clark, JB; Cooper, JM; Hayes, DJ; Morgan-Hughes, JA; Petty, RK | 1 |
Cadman, TE; Kinoshita, M | 1 |
Copeland, W; Kelly, S; Smith, RO | 1 |
Kinoshita, M | 1 |
DeMyer, W; Goebel, HH; Muller, J | 1 |
Faris, AA; Hooshmand, H; Martinez, AJ | 1 |
Aberle, ED; Hendricks, HB; Jones, DJ; Martin, TG | 1 |
Dettbarn, WD; Fenichel, GM; Newman, TM | 1 |
Gordon, AS; Humphrey, JG; Rewcastle, NB; Stewart, BM | 1 |
Berthillier, G; Gautheron, D; Robert, JM | 1 |
Dube, V; Hunter, DT; Knight, JA | 1 |
3 review(s) available for nad and Muscular Diseases
Article | Year |
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NAD
Topics: Aging; Animals; Epigenesis, Genetic; Mice; Muscle, Skeletal; Muscular Diseases; NAD; Poly(ADP-ribose) Polymerases | 2022 |
Need for NAD
Topics: Animals; Disease Models, Animal; Humans; Lamin Type A; Laminopathies; Muscle, Skeletal; Muscle, Striated; Muscular Diseases; Muscular Dystrophy, Emery-Dreifuss; NAD; Nuclear Lamina | 2020 |
A need for NAD+ in muscle development, homeostasis, and aging.
Topics: Aging; Animals; Homeostasis; Humans; Intracellular Space; Muscle Development; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; NAD; Niacinamide; Nicotinamide Phosphoribosyltransferase; Pyridinium Compounds; Regeneration; Signal Transduction | 2018 |
1 trial(s) available for nad and Muscular Diseases
Article | Year |
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Structural changes in male trapezius muscle with work-related myalgia.
Topics: Adenosine Triphosphatases; Adult; Capillaries; Electron Transport Complex IV; Humans; Immunohistochemistry; Male; Middle Aged; Muscle Fibers, Fast-Twitch; Muscle Fibers, Skeletal; Muscle Fibers, Slow-Twitch; Muscle, Skeletal; Muscular Diseases; NAD; Occupational Diseases; Pain; Regional Blood Flow; Shoulder | 1998 |
28 other study(ies) available for nad and Muscular Diseases
Article | Year |
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Metabolite profile based on
Topics: Amino Acids; Animals; Anserine; Carbohydrates; Chickens; Creatine; Muscular Diseases; NAD; Pectoralis Muscles; Poultry Products; Proton Magnetic Resonance Spectroscopy | 2020 |
GNE myopathy in the bedouin population of Kuwait: Genetics, prevalence, and clinical description.
Topics: Adult; Creatine Kinase; Family Health; Female; Humans; Kuwait; Magnetic Resonance Imaging; Male; Multienzyme Complexes; Muscle, Skeletal; Muscular Diseases; Mutation; Myosin Heavy Chains; NAD; Nerve Fibers; Retrospective Studies; Young Adult | 2018 |
The clinical spectrum of
Topics: Adolescent; Adult; Aged; Calcium; Calcium-Binding Proteins; Calsequestrin; Family Health; Female; Genetic Testing; Humans; Lysosomal Storage Diseases; Magnetic Resonance Imaging; Male; Microscopy, Electron, Transmission; Middle Aged; Mitochondrial Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; NAD; Young Adult | 2018 |
Potassium dependent rescue of a myopathy with core-like structures in mouse.
Topics: Animals; Biological Transport; Biomarkers; Biopsy; Calcium; Diet; Ethylnitrosourea; Gene Expression Regulation; Glyburide; Heterozygote; Homeostasis; Humans; KATP Channels; Mice, Inbred C57BL; Mitochondria; Muscle, Skeletal; Muscular Diseases; Mutation; Myopathy, Central Core; NAD; Phenotype; Potassium; RNA, Messenger; Ryanodine Receptor Calcium Release Channel | 2015 |
The PPARα agonists fenofibrate and CP-778875 cause increased β-oxidation, leading to oxidative injury in skeletal and cardiac muscle in the rat.
Topics: Animals; Blood Chemical Analysis; Body Weight; Dose-Response Relationship, Drug; Female; Fenofibrate; Heart; Liver; Male; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Myocardium; NAD; Oxidative Stress; Peroxisomes; PPAR alpha; Rats; Rats, Sprague-Dawley; Toxicity Tests; Troponin I | 2012 |
On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.
Topics: Adenine; Adult; Amino Acid Sequence; Base Sequence; Blotting, Western; Cell Line; Cytoplasm; Cytoskeleton; Desmin; DNA; DNA Mutational Analysis; DNA, Complementary; Fluorescent Antibody Technique, Indirect; Frameshift Mutation; Genes, Dominant; Heterozygote; Humans; Male; Microscopy, Immunoelectron; Mitochondria; Molecular Sequence Data; Muscle, Skeletal; Muscular Diseases; Mutagenesis, Site-Directed; Mutation; NAD; Polymerase Chain Reaction; Transfection | 2003 |
HUMAN MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA.
Topics: Acid Phosphatase; Adenosine Triphosphatases; Biopsy; Child; Electron Transport Complex IV; Electrons; Histocytochemistry; Humans; Lysosomes; Microscopy; Microscopy, Electron; Mitochondria; Mitochondrial Diseases; Muscles; Muscular Diseases; NAD; Oxidoreductases; Succinate Dehydrogenase | 1964 |
CENTRAL "CORE" DISEASE OF SKELETAL MUSCLE. ULTRASTRUCTURAL AND CYTOCHEMICAL OBSERVATIONS IN TWO CASES.
Topics: Adenosine Triphosphatases; Child; Electron Transport Complex IV; Genetics, Medical; Histocytochemistry; Humans; Metabolism; Muscle, Skeletal; Muscular Diseases; NAD; Pathology; Phosphotransferases; Succinate Dehydrogenase | 1965 |
Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.
Topics: Aged; Amyotrophic Lateral Sclerosis; Blotting, Western; Creatine; Cysteine; DNA Mutational Analysis; Family Health; Female; Glycine; Humans; Immunohistochemistry; Muscular Diseases; Mutation; Myosins; NAD; Phenotype; Superoxide Dismutase; Superoxide Dismutase-1; Ubiquitin | 2006 |
A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities.
Topics: Adult; Biopsy; Blepharoptosis; Cell Nucleus; Electrooculography; Humans; Inclusion Bodies; Male; Mitochondria, Muscle; Muscles; Muscular Diseases; NAD; Ophthalmoplegia | 1980 |
Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain.
Topics: Biopsy; Brain Diseases; Cytochromes; Electron Transport; Female; Humans; Male; Middle Aged; Mitochondria, Muscle; Muscular Diseases; NAD; Oxidation-Reduction; Pyruvate Dehydrogenase Complex; Respiration | 1982 |
Pathological mechanisms implicated in localized female trapezius myalgia.
Topics: Adult; Capillaries; Electron Transport Complex IV; Female; Humans; Mitochondria, Muscle; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Diseases; NAD; Shoulder; Shoulder Pain | 1998 |
Cores in hypothyroid myopathy: a clinical, histological and immunofluorescence study.
Topics: Adult; Aged; Female; Fluorescent Antibody Technique; Humans; Hypothyroidism; Male; Microscopy, Electron; Middle Aged; Muscle, Skeletal; Muscular Diseases; NAD; Neural Cell Adhesion Molecules; Tetrazolium Salts | 2000 |
A myopathy associated with myotonia in the dog.
Topics: Animals; Cell Nucleus; Connective Tissue; Dog Diseases; Dogs; Histocytochemistry; Hyalin; Muscles; Muscular Diseases; Myotonia; NAD; Necrosis; Neuromuscular Diseases; Regeneration; Succinate Dehydrogenase | 1975 |
Multicore disease. Report of a case with lack of fibre type differentiation.
Topics: Adenosine Triphosphatases; Child; Child, Preschool; Histocytochemistry; Humans; Leg; Male; Muscles; Muscular Diseases; NAD | 1978 |
Magnetic resonance spectroscopy of normal and diseased muscles.
Topics: Acidosis; Adenine Nucleotides; Age Factors; Animals; Cattle; Cytochrome b Group; Energy Metabolism; Humans; Immobilization; Kinetics; Magnetic Resonance Spectroscopy; Mitochondria, Muscle; Muscles; Muscular Diseases; Muscular Dystrophies; NAD; Phosphates; Phosphocreatine; Phosphofructokinase-1; Physical Exertion | 1986 |
Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome.
Topics: Acidosis, Lactic; Adolescent; Brain Diseases; Cerebrovascular Disorders; Humans; Male; Mitochondria, Muscle; Muscular Diseases; NAD; NAD(P)H Dehydrogenase (Quinone); Quinone Reductases; Syndrome | 1987 |
Chronic administration of the oral hypoglycaemic agent diphenyleneiodonium to rats. An animal model of impaired oxidative phosphorylation (mitochondrial myopathy).
Topics: Administration, Oral; Animals; Cytochromes; Disease Models, Animal; Hypoglycemic Agents; Male; Mitochondria; Muscles; Muscular Diseases; NAD; Onium Compounds; Oxidative Phosphorylation; Pyruvate Dehydrogenase Complex; Rats; Rats, Inbred Strains | 1988 |
Myotubular myopathy.
Topics: Adenosine Triphosphatases; Aminosalicylic Acids; Child; Female; Fetus; Glucosyltransferases; Humans; Infant, Newborn; Microscopy, Electron; Muscles; Muscular Diseases; Myofibrils; NAD; Succinate Dehydrogenase | 1968 |
A fluorescent spot test for creatine kinase.
Topics: Buffers; Chemical Phenomena; Chemistry; Clinical Enzyme Tests; Clinical Laboratory Techniques; Creatine Kinase; Female; Fluorescence; Humans; Indicators and Reagents; Male; Mass Screening; Muscular Diseases; Muscular Dystrophies; NAD; Neuromuscular Diseases; Spectrophotometry; Time Factors | 1968 |
[Atlas of myohistochemistry. 12. Congenital myopathy. 2].
Topics: Adenosine Triphosphatases; Child, Preschool; Female; Histocytochemistry; Humans; Infant; Male; Muscular Diseases; Muscular Dystrophies; NAD | 1971 |
Myopathy associated with Marfan's syndrome. Fine structural and histochemical observations.
Topics: Adenosine Triphosphatases; Adolescent; Biopsy; Glycerolphosphate Dehydrogenase; Glycogen; Histocytochemistry; Humans; Male; Marfan Syndrome; Microscopy, Electron; Mitochondria, Muscle; Muscles; Muscular Diseases; Myofibrils; NAD; Sarcolemma; Sarcoplasmic Reticulum | 1973 |
Acute alcoholic myopathy. Enzyme histochemistry and electron microscopic findings.
Topics: Acute Disease; Adenosine Triphosphatases; Alcoholism; Glycerolphosphate Dehydrogenase; Histocytochemistry; Humans; Inclusion Bodies; Male; Microscopy, Electron; Mitochondria, Muscle; Muscular Diseases; Myosins; NAD | 1973 |
Muscle fiber type, rigor development and bone strength in dobule muscled cattle.
Topics: Adenosine Triphosphatases; Animals; Biomechanical Phenomena; Bone and Bones; Cattle; Cattle Diseases; Histocytochemistry; Hypertrophy; Male; Metacarpus; Muscles; Muscular Diseases; Myofibrils; NAD; Phenotype; Postmortem Changes | 1973 |
An experimental myopathy secondary to excessive acetylcholine release.
Topics: Acetylcholine; Adenosine Triphosphatases; Animals; Carbachol; Female; Guanidines; L-Lactate Dehydrogenase; Membrane Potentials; Muscles; Muscular Diseases; NAD; Necrosis; Neuromuscular Junction; Paraoxon; Rats; Sciatic Nerve | 1974 |
Chronic benign congenital myopathy: fingerprint body type.
Topics: Acid Phosphatase; Adenosine Triphosphatases; Chronic Disease; Creatine Kinase; Female; Glycogen; Histocytochemistry; Humans; Inclusion Bodies; Lipid Metabolism; Lipoproteins; Microscopy, Electron; Middle Aged; Muscles; Muscular Diseases; Myofibrils; NAD; Succinate Dehydrogenase | 1974 |
[Phosphorylated fractions and free adenine nucleotides of myopathic muscles in children].
Topics: Adenine Nucleotides; Child; Child, Preschool; Creatine Kinase; Fructose-Bisphosphate Aldolase; Humans; Muscles; Muscular Diseases; NAD; NADP; Phosphates; Phosphocreatine | 1967 |
Automated spectrophotometric assay of serum lactic dehydrogenase and hydroxybutyric dehydrogenase with clinical evaluation.
Topics: Automation; Heart Diseases; Humans; Hydroxybutyrate Dehydrogenase; Keto Acids; L-Lactate Dehydrogenase; Lung Diseases; Methods; Muscular Diseases; NAD; NADP; Pyruvates; Spectrophotometry | 1968 |