carnitine has been researched along with Muscular Dystrophy in 32 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "We determined levels of purines, purine metabolites, related enzymes and carnitine in muscle of 8 untreated Duchenne muscular dystrophy (DMD) patients, 12 allopurinol-treated DMD patients and 12 age-matched controls." | 7.69 | Purine and carnitine metabolism in muscle of patients with Duchenne muscular dystrophy. ( Camiña, F; Castro-Gago, M; Novo-Rodriguez, MI; Rodriguez-Segade, S, 1995) |
| "The effects of a single oral dose of carnitine on fasting-induced ketosis was investigated in four normal individuals, five patients with muscular dystrophy, and one patient with a generalized cytochrome c oxidase deficiency." | 7.67 | Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency. ( Hoganson, GE; Paulson, DJ; Peters, H; Shug, AL; Sufit, R; Traxler, J, 1988) |
| "Muscle carnitine deficiency was found in 12 children affected with Duchenne muscular dystrophy (DMD), the diagnosis being made at a preclinical stage or at the beginning of the clinical symptoms." | 7.66 | Carnitine metabolism in early stages of Duchenne muscular dystrophy. ( Berthillier, G; Carrier, HN; Eichenberger, D; Got, R; Guibaud, P, 1982) |
| "Neuromuscular diseases accompanied by muscle atrophy are likely to lead to secondary carnitine deficiency, owing to the reduced amount of total carnitine stored in the body." | 5.91 | A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleeding. ( Goto, K; Hiramatsu, M; Imai, K; Korematsu, S; Uchiyama, SI; Uemura, A; Wasada, R, 2023) |
| "We determined levels of purines, purine metabolites, related enzymes and carnitine in muscle of 8 untreated Duchenne muscular dystrophy (DMD) patients, 12 allopurinol-treated DMD patients and 12 age-matched controls." | 3.69 | Purine and carnitine metabolism in muscle of patients with Duchenne muscular dystrophy. ( Camiña, F; Castro-Gago, M; Novo-Rodriguez, MI; Rodriguez-Segade, S, 1995) |
| "The effects of a single oral dose of carnitine on fasting-induced ketosis was investigated in four normal individuals, five patients with muscular dystrophy, and one patient with a generalized cytochrome c oxidase deficiency." | 3.67 | Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency. ( Hoganson, GE; Paulson, DJ; Peters, H; Shug, AL; Sufit, R; Traxler, J, 1988) |
| "Muscle carnitine deficiency was found in 12 children affected with Duchenne muscular dystrophy (DMD), the diagnosis being made at a preclinical stage or at the beginning of the clinical symptoms." | 3.66 | Carnitine metabolism in early stages of Duchenne muscular dystrophy. ( Berthillier, G; Carrier, HN; Eichenberger, D; Got, R; Guibaud, P, 1982) |
| "Neuromuscular diseases accompanied by muscle atrophy are likely to lead to secondary carnitine deficiency, owing to the reduced amount of total carnitine stored in the body." | 1.91 | A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleeding. ( Goto, K; Hiramatsu, M; Imai, K; Korematsu, S; Uchiyama, SI; Uemura, A; Wasada, R, 2023) |
| "Muscle weakness is a nonspecific finding of myopathy of any etiology that include iatrogenic, toxic, endocrinological, infectious, immunologic, and metabolic disorders." | 1.51 | Two cases of glutaric aciduria type II: how to differentiate from inflammatory myopathies? ( Armagan, B; Erden, A; Kalyoncu, U; Karadag, O; Koca, M; Ozdamar, S; Sari, A; Yildiz, F, 2019) |
| "Severe pneumonia was the initial diagnosis." | 1.42 | Refractory Hyperlactatemia with Organ Insufficiency in Lipid Storage Myopathy. ( He, W; Li, Y; Liang, W; Liang, X; Liu, X; Xu, Y; Zhong, N; Zhou, L, 2015) |
| "Epidemiology of muscular dystrophies has been important in the prevention of these diseases." | 1.26 | [Muscular diseases: epidemiology of progressive muscular dystrophies]. ( Armani, M; Schergna, E, 1981) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 22 (68.75) | 18.7374 |
| 1990's | 2 (6.25) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 7 (21.88) | 24.3611 |
| 2020's | 1 (3.13) | 2.80 |
| Authors | Studies |
|---|---|
| Uchiyama, SI | 1 |
| Korematsu, S | 1 |
| Wasada, R | 1 |
| Imai, K | 1 |
| Uemura, A | 1 |
| Hiramatsu, M | 1 |
| Goto, K | 1 |
| Han, J | 1 |
| Song, X | 1 |
| Lu, S | 1 |
| Ji, G | 1 |
| Xie, Y | 1 |
| Wu, H | 1 |
| Pinn, TL | 1 |
| Divers, TJ | 1 |
| Southard, T | 1 |
| De Bernardis, NP | 1 |
| Wakshlag, JJ | 1 |
| Valberg, S | 1 |
| Koca, M | 1 |
| Erden, A | 1 |
| Armagan, B | 1 |
| Sari, A | 1 |
| Yildiz, F | 1 |
| Ozdamar, S | 1 |
| Kalyoncu, U | 1 |
| Karadag, O | 1 |
| Xu, Y | 1 |
| Zhou, L | 1 |
| Liang, W | 1 |
| He, W | 1 |
| Liu, X | 1 |
| Liang, X | 1 |
| Zhong, N | 1 |
| Li, Y | 1 |
| Angelini, C | 1 |
| Nascimbeni, AC | 1 |
| Cenacchi, G | 1 |
| Tasca, E | 1 |
| Parsonage, WA | 1 |
| Mikli, JE | 1 |
| Nisbet, JC | 1 |
| Hamilton-Craig, C | 1 |
| Marshall, GA | 1 |
| Saini-Chohan, HK | 1 |
| Mitchell, RW | 1 |
| Vaz, FM | 1 |
| Zelinski, T | 1 |
| Hatch, GM | 1 |
| Berthillier, G | 1 |
| Eichenberger, D | 1 |
| Carrier, HN | 1 |
| Guibaud, P | 1 |
| Got, R | 1 |
| Carroll, JE | 1 |
| Villadiego, A | 1 |
| Brooke, MH | 1 |
| Cornelio, F | 1 |
| Dworzak, F | 1 |
| Morandi, L | 1 |
| Fedrizzi, E | 1 |
| Balestrini, MR | 1 |
| Gondoni, L | 1 |
| Schmidt, A | 1 |
| Hässler, A | 1 |
| Schergna, E | 1 |
| Armani, M | 1 |
| Buxton, PH | 1 |
| Smyth, DP | 1 |
| Binder, S | 1 |
| Sluga, E | 1 |
| Camiña, F | 1 |
| Novo-Rodriguez, MI | 1 |
| Rodriguez-Segade, S | 1 |
| Castro-Gago, M | 1 |
| Porschke, H | 1 |
| Kress, W | 1 |
| Reichmann, H | 1 |
| Goebel, HH | 1 |
| Grimm, T | 1 |
| Jato-Rodriguez, J | 1 |
| Liang, CR | 1 |
| Lin, CH | 1 |
| Hudson, AJ | 1 |
| Strickland, KP | 1 |
| Claireaux, AE | 1 |
| Lake, BD | 1 |
| Pande, SV | 1 |
| Mitchell, ME | 1 |
| Kobayashi, T | 1 |
| Shinnoh, N | 1 |
| Mawatari, S | 1 |
| Bradley, WG | 1 |
| Tomlinson, BE | 1 |
| Hardy, M | 1 |
| Borum, PR | 1 |
| Broquist, HP | 1 |
| Roelops, RJ | 1 |
| DiMauro, S | 2 |
| Rowland, LP | 2 |
| Paulson, DJ | 1 |
| Hoganson, GE | 1 |
| Traxler, J | 1 |
| Sufit, R | 1 |
| Peters, H | 1 |
| Shug, AL | 1 |
| Schmickel, RD | 1 |
| Rabinovitch, MA | 1 |
| Kalff, V | 1 |
| Allen, R | 1 |
| Rosenthal, A | 1 |
| Albers, J | 1 |
| Das, SK | 1 |
| Pitt, B | 1 |
| Swanson, DP | 1 |
| Mangner, T | 1 |
| Rogers, WL | 1 |
| Maebashi, M | 1 |
| Kawamura, N | 1 |
| Yoshinaga, K | 1 |
| Scott, C | 1 |
| Penn, AS | 1 |
| Wrogemann, K | 1 |
| Blanchaer, MC | 1 |
| Jacobson, BE | 1 |
4 reviews available for carnitine and Muscular Dystrophy
| Article | Year |
|---|---|
Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.
Topics: Adult; Animals; Cardiolipins; Cardiomyopathies; Carnitine; Child, Preschool; Desmin; Dystrophin; Fab | 2012 |
Pathology of muscle.
Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Denervation; Female; Gl | 1980 |
[Carnitine: its role and its action in disease].
Topics: Animals; Carnitine; Carnitine Acyltransferases; Energy Metabolism; Fatty Acids; Humans; Mitochondria | 1977 |
Carnitine metabolism in human subjects. III. Metabolism in disease.
Topics: Adolescent; Adult; Animals; Carnitine; Carnitine Acyltransferases; Child; Diabetes Mellitus; Diabeti | 1978 |
1 trial available for carnitine and Muscular Dystrophy
| Article | Year |
|---|---|
Functional evaluation of Duchenne muscular dystrophy: proposal for a protocol.
Topics: Carnitine; Child; Child, Preschool; Clinical Trials as Topic; Double-Blind Method; Follow-Up Studies | 1982 |
27 other studies available for carnitine and Muscular Dystrophy
| Article | Year |
|---|---|
A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleeding.
Topics: Amino Acids; Carnitine; Fatty Acids; Gastrointestinal Hemorrhage; Humans; Male; Muscular Atrophy; Mu | 2023 |
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study.
Topics: Adolescent; Adult; Carnitine; Child; China; Electron-Transferring Flavoproteins; Female; Humans; Hyp | 2019 |
Persistent hypoglycemia associated with lipid storage myopathy in a paint foal.
Topics: Animals; Carnitine; Diagnosis, Differential; Fatal Outcome; Female; Horse Diseases; Horses; Hypoglyc | 2018 |
Two cases of glutaric aciduria type II: how to differentiate from inflammatory myopathies?
Topics: Acyl-CoA Dehydrogenase; Adolescent; Biopsy; Carnitine; Diagnosis, Differential; Female; Humans; Late | 2019 |
Refractory Hyperlactatemia with Organ Insufficiency in Lipid Storage Myopathy.
Topics: Adolescent; Bronchitis; Carnitine; Female; Humans; Hyperlactatemia; Lipid Metabolism, Inborn Errors; | 2015 |
Lipolysis and lipophagy in lipid storage myopathies.
Topics: Adolescent; Adult; Aged; Autophagy; Cardiomyopathies; Carnitine; Carnitine O-Palmitoyltransferase; C | 2016 |
A 61-Year-Old Woman with Muscle Fatigue and Increased Cardiac Troponin.
Topics: Carnitine; Creatine Kinase; Female; Humans; Lipid Metabolism, Inborn Errors; Middle Aged; Multiple A | 2017 |
Carnitine metabolism in early stages of Duchenne muscular dystrophy.
Topics: Carboxylic Ester Hydrolases; Carnitine; Carnitine O-Palmitoyltransferase; Cell Membrane; Child; Chil | 1982 |
Increased long chain acyl CoA in Duchenne muscular dystrophy.
Topics: Acyl Coenzyme A; Carnitine; Humans; Muscular Dystrophies | 1983 |
[Lipid storage myopathy--a contribution to the problem of the differential diagnosis of muscle dystrophy (Duchenne)].
Topics: Age Factors; Carnitine; Child; Diagnosis, Differential; Humans; Lipid Metabolism; Male; Muscular Atr | 1983 |
[Muscular diseases: epidemiology of progressive muscular dystrophies].
Topics: Adenosine Monophosphate; Carnitine; Carnitine O-Palmitoyltransferase; Consanguinity; Dietary Fats; G | 1981 |
Quantitative electromyography in babies and young children with primary muscle disease and neurogenic lesions.
Topics: Anterior Horn Cells; Carnitine; Child; Child Development; Child, Preschool; Dermatomyositis; Diagnos | 1982 |
[Differential diagnosis of ocular myopathies].
Topics: Adolescent; Adult; Carnitine; Diagnosis, Differential; Electromyography; Female; Humans; Muscular Di | 1980 |
Purine and carnitine metabolism in muscle of patients with Duchenne muscular dystrophy.
Topics: Adolescent; Allopurinol; Carnitine; Child; Child, Preschool; Creatine Kinase; Energy Metabolism; Enz | 1995 |
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency.
Topics: Adult; Aged; Biopsy; Carnitine; Chromosomes, Human, Pair 14; Electromyography; Family Health; Female | 1997 |
Comparison of the intermediary metabolism of fatty acids in denervated and dystrophic murine skeletal muscle.
Topics: Acyl-CoA Dehydrogenases; Animals; Carnitine; Electron Transport Complex IV; Lipase; Lipid Metabolism | 1975 |
Muscle disorders in the floppy child.
Topics: Biopsy; Carnitine; Child; Glycogen Storage Disease; Humans; Infant; Muscles; Muscular Atrophy; Muscu | 1978 |
Carnitine in Duchenne muscular dystrophy.
Topics: Adolescent; Carnitine; Child; Creatinine; Female; Humans; Male; Muscular Dystrophies; Reference Valu | 1979 |
Further studies of mitochondrial and lipid storage myopathies.
Topics: Adolescent; Adult; Brain; Carnitine; Female; Humans; Lipidoses; Male; Middle Aged; Mitochondria, Mus | 1978 |
Muscle carnitine levels in neuromuscular disease.
Topics: Carnitine; Humans; Methods; Muscles; Muscular Atrophy; Muscular Dystrophies; Neuromuscular Diseases | 1977 |
Urinary excretion of carnitine in Duchenne muscular dystrophy.
Topics: Adolescent; Adult; Carnitine; Cell Membrane; Child; Child, Preschool; Humans; Male; Muscles; Muscula | 1976 |
Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency.
Topics: Adult; Blood Glucose; Carnitine; Cytochrome-c Oxidase Deficiency; Fasting; Fatty Acids, Nonesterifie | 1988 |
Clinical genetics conference: progress in understanding muscle disease.
Topics: Carnitine; Child; Humans; Magnetic Resonance Spectroscopy; Mitochondria, Muscle; Muscles; Muscular D | 1986 |
omega-123I-hexadecanoic acid metabolic probe of cardiomyopathy.
Topics: Adolescent; Adult; Aged; Alcoholism; Atrial Fibrillation; Cardiomyopathies; Cardiomyopathy, Dilated; | 1985 |
Urinary excretion of carnitine in progressive muscular dystrophy.
Topics: Adolescent; Adrenocorticotropic Hormone; Adult; Age Factors; Carnitine; Child; Female; Humans; Male; | 1974 |
Serum carnitine. An index of muscle destruction in man.
Topics: Adolescent; Adult; Alanine Transaminase; Aspartate Aminotransferases; Carbon Isotopes; Carnitine; Ch | 1973 |
Oxidative phosphorylation in cardiomyopathic hamsters.
Topics: Adenosine Diphosphate; Animals; Cardiomyopathies; Carnitine; Cricetinae; Glutamates; Heart Failure; | 1972 |