carnitine has been researched along with Neuromuscular Diseases in 28 studies
Neuromuscular Diseases: A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Free and total carnitine serum concentrations and urinary excretion were examined in patients with various neuromuscular diseases." | 7.66 | Carnitine intake and excretion in neuromuscular diseases. ( Brooke, MH; Carroll, JE; Janes, NJ; Shumate, JB, 1981) |
| " Four dynamic syndromes are currently recognized: 1) defective carbohydrate utilization, due to block of glycogenolysis or glycolysis; 2) defective lipid utilization, due to deficiency of the mitochondrial translocation of long-chain fatty acids (carnitine palmityltransferase deficiency); 3) lactic acidosis, due to defects of mitochondrial electron transport enzymes and possibly other unidentified defects; and 4) abnormal adenine nucleotide metabolism, exemplified by adenylate deaminase deficiency." | 3.67 | Clinical disorders of muscle energy metabolism. ( Layzer, RB; Lewis, SF, 1984) |
| "Free and total carnitine serum concentrations and urinary excretion were examined in patients with various neuromuscular diseases." | 3.66 | Carnitine intake and excretion in neuromuscular diseases. ( Brooke, MH; Carroll, JE; Janes, NJ; Shumate, JB, 1981) |
| "Barth syndrome is an X-linked recessive condition characterized by skeletal myopathy, cardiomyopathy, proportionate short stature, and recurrent neutropenia, but with normal cognitive function." | 1.29 | Barth syndrome: clinical observations and genetic linkage studies. ( Becker, LE; Bridge, PJ; Christodoulou, J; Clarke, JT; Jay, V; Lehotay, DC; McInnes, RR; Platt, BA; Robinson, BH; Wilson, G, 1994) |
| "So, in four patients with congestive cardiomyopathy, biopsy of the endocardium has enabled to demonstrate a chronic inflammation of the myocardium in one patient." | 1.27 | [Congestive cardiomyopathies in children. Natural history and studies]. ( Boutet, M; Cloutier, A; Delisle, G; Guay, JM, 1986) |
| "Free carnitine was extremely reduced in muscle and liver and just below normal level in plasma while there was a tenfold elevation of long-chain carnitine esters in plasma too." | 1.26 | Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical study. ( Cornelio, F; DiDonato, S; Mora, M; Negri, S; Peluchetti, D; Rimoldi, M; Testa, D, 1981) |
| "Carnitine was never detected in growth medium." | 1.26 | Muscular carnitine synthesis and palmitate metabolism in vitro. ( Cerri, C; Meola, G; Scarlato, G; Scarpini, E, 1978) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 24 (85.71) | 18.7374 |
| 1990's | 2 (7.14) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cassol, G | 1 |
| Godinho, DB | 1 |
| de Zorzi, VN | 1 |
| Farinha, JB | 1 |
| Della-Pace, ID | 1 |
| de Carvalho Gonçalves, M | 1 |
| Oliveira, MS | 1 |
| Furian, AF | 1 |
| Fighera, MR | 1 |
| Royes, LFF | 1 |
| Béhin, A | 1 |
| Acquaviva-Bourdain, C | 1 |
| Souvannanorath, S | 1 |
| Streichenberger, N | 1 |
| Attarian, S | 1 |
| Bassez, G | 1 |
| Brivet, M | 1 |
| Fouilhoux, A | 1 |
| Labarre-Villa, A | 1 |
| Laquerrière, A | 1 |
| Pérard, L | 1 |
| Kaminsky, P | 1 |
| Pouget, J | 1 |
| Rigal, O | 1 |
| Vanhulle, C | 1 |
| Eymard, B | 1 |
| Vianey-Saban, C | 1 |
| Laforêt, P | 1 |
| Cornelio, F | 1 |
| Peluchetti, D | 1 |
| Rimoldi, M | 1 |
| Testa, D | 1 |
| Mora, M | 1 |
| Negri, S | 1 |
| DiDonato, S | 1 |
| Czyzewski, K | 1 |
| Stern, LZ | 1 |
| Sadeh, M | 1 |
| Bahl, JJ | 1 |
| Layzer, RB | 1 |
| Lewis, SF | 1 |
| Cumming, WJ | 1 |
| Morooka, K | 1 |
| Gamstorp, I | 1 |
| Cerri, C | 2 |
| Meola, G | 2 |
| Scarlato, G | 2 |
| Angelini, C | 2 |
| Battistella, PA | 1 |
| Laverda, A | 1 |
| Pierobon-Bormioli, S | 1 |
| Salviati, G | 1 |
| Vergani, L | 1 |
| Buxton, PH | 1 |
| Kamieniecka, Z | 1 |
| Schmalbruch, H | 1 |
| Shumate, JB | 2 |
| Carroll, JE | 2 |
| Brooke, MH | 2 |
| Choksi, RM | 1 |
| McCarty, MF | 1 |
| Smyth, DP | 1 |
| Janes, NJ | 1 |
| Christodoulou, J | 1 |
| McInnes, RR | 1 |
| Jay, V | 1 |
| Wilson, G | 1 |
| Becker, LE | 1 |
| Lehotay, DC | 1 |
| Platt, BA | 1 |
| Bridge, PJ | 1 |
| Robinson, BH | 1 |
| Clarke, JT | 1 |
| Gonzalez-Crespo, MR | 1 |
| Arenas, J | 1 |
| Gomez-Reino, JJ | 1 |
| Campos, Y | 1 |
| Borstein, B | 1 |
| Martin, MA | 1 |
| Cabello, A | 1 |
| Garcia-Rayo, R | 1 |
| Ricoy, JR | 1 |
| Scarpini, E | 1 |
| Borum, PR | 1 |
| Broquist, HP | 1 |
| Roelops, RJ | 1 |
| Amit, R | 1 |
| Gutman, A | 1 |
| Shapira, Y | 1 |
| Trevisan, CP | 1 |
| Reichmann, H | 1 |
| DeVivo, DC | 1 |
| DiMauro, S | 1 |
| Shah, A | 1 |
| Sahgal, V | 1 |
| Sahgal, S | 1 |
| Subramani, V | 1 |
| Kochar, H | 1 |
| Cloutier, A | 1 |
| Boutet, M | 1 |
| Guay, JM | 1 |
| Delisle, G | 1 |
| Askanas, V | 1 |
| Engel, WK | 1 |
| Kwan, HH | 1 |
| Reddy, NB | 1 |
| Husainy, T | 1 |
| Carlo, J | 1 |
| Siddique, T | 1 |
| Schwartzman, RJ | 1 |
| Hanna, CJ | 1 |
| Martin, JJ | 1 |
| Vercruyssen, A | 1 |
| de Barsy, T | 1 |
| Ceuterick, C | 1 |
| Markesbery, WR | 1 |
| McQuillen, MP | 1 |
| Procopis, PG | 1 |
| Harrison, AR | 1 |
| Engel, AG | 2 |
5 reviews available for carnitine and Neuromuscular Diseases
| Article | Year |
|---|---|
Potential therapeutic implications of ergogenic compounds on pathophysiology induced by traumatic brain injury: A narrative review.
Topics: Animals; Arginine; Brain Injuries, Traumatic; Caffeine; Carnitine; Central Nervous System Stimulants | 2019 |
[Benign myopathy in children].
Topics: Acidosis; Adolescent; Adult; Age Factors; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, | 1982 |
Non-dystrophic, myogenic myopathies with onset in infancy or childhood. A review of some characteristic syndromes.
Topics: Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Dermatomyositis; Endocrine Sys | 1982 |
Pathology of muscle.
Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Denervation; Female; Gl | 1980 |
Neuromuscular disorders with abnormal muscle mitochondria.
Topics: Animals; Carnitine; Diagnosis, Differential; Female; Humans; Lipid Metabolism; Male; Metabolic Disea | 1980 |
23 other studies available for carnitine and Neuromuscular Diseases
| Article | Year |
|---|---|
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease.
Topics: Adult; Age of Onset; Biopsy; Carnitine; Electromyography; Electron-Transferring Flavoproteins; Exerc | 2016 |
Systemic carnitine deficiency with peripheral nerve involvement morphological and biochemical study.
Topics: Adult; Carnitine; Humans; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Liver; Male; Mitochondr | 1981 |
Changes in muscle carnitine during regeneration.
Topics: Animals; Bupivacaine; Carnitine; Male; Muscles; Neuromuscular Diseases; Rats; Rats, Inbred Strains; | 1984 |
Clinical disorders of muscle energy metabolism.
Topics: Acidosis; Adenine Nucleotides; Carbohydrate Metabolism; Carnitine; Energy Metabolism; Humans; Lactat | 1984 |
Lipid myopathy. Case report and review.
Topics: Adult; Animals; Carnitine; Diagnosis, Differential; Humans; Lipid Metabolism; Male; Muscles; Neuromu | 1984 |
Biochemical and morphological studies on a case of systemic carnitine deficiency.
Topics: Adult; Brain Diseases, Metabolic; Carnitine; Humans; Liver; Male; Neuromuscular Diseases | 1981 |
Fatal lipid storage with abnormal mitochondria in an infant.
Topics: Brain Diseases, Metabolic; Carnitine; Glycogen; Humans; Infant; Lipid Metabolism; Lipid Metabolism, | 1981 |
Palmitate oxidation in human muscle: comparison to CPT and carnitine.
Topics: Acyltransferases; Adolescent; Adult; Aged; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child | 1982 |
A note on "orthomolecular aids for dieting"--myasthenic syndrome due to dl-carnitine.
Topics: Animals; Anuria; Carnitine; Humans; Neuromuscular Diseases; Obesity; Rats; Syndrome | 1982 |
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 |
Carnitine intake and excretion in neuromuscular diseases.
Topics: Adolescent; Adult; Carnitine; Carnitine O-Palmitoyltransferase; Creatinine; Diet; Female; Humans; Ki | 1981 |
Barth syndrome: clinical observations and genetic linkage studies.
Topics: Abnormalities, Multiple; Acids; Cardiomyopathy, Dilated; Carnitine; Diseases in Twins; Dwarfism; Ele | 1994 |
Muscle dysfunction in elderly individuals with hip fracture.
Topics: Age Factors; Aged; Aged, 80 and over; Aging; Carnitine; Electron Transport; Female; Hip Fractures; H | 1999 |
Muscular carnitine synthesis and palmitate metabolism in vitro.
Topics: Carnitine; Cells, Cultured; Humans; Muscles; Neuromuscular Diseases; Palmitates; Palmitic Acids | 1978 |
Muscle carnitine levels in neuromuscular disease.
Topics: Carnitine; Humans; Methods; Muscles; Muscular Atrophy; Muscular Dystrophies; Neuromuscular Diseases | 1977 |
Muscle carnitine deficiency in neurogenic atrophy.
Topics: Carnitine; Child; Child, Preschool; Humans; Infant; Muscles; Neuromuscular Diseases | 1989 |
Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency.
Topics: Acyltransferases; Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child, Preschool; Coenzyme A L | 1985 |
Variability of mitochondrial cytochemistry in human neuromuscular diseases.
Topics: Calcium; Carnitine; Carnitine O-Palmitoyltransferase; Histocytochemistry; Humans; Kearns-Sayre Syndr | 1988 |
[Congestive cardiomyopathies in children. Natural history and studies].
Topics: Adolescent; Biopsy; Cardiomyopathy, Dilated; Carnitine; Child; Child, Preschool; Follow-Up Studies; | 1986 |
Autosomal dominant syndrome of lipid neuromyopathy with normal carnitine: successful treatment with long-chain fatty-acid-free diet.
Topics: Adolescent; Adult; Carnitine; Child; Fatty Acids; Female; Humans; Male; Neuromuscular Diseases | 1985 |
Muscle carnitine deficiency in old age. Case report and therapeutic results.
Topics: Aged; Biopsy; Carnitine; Electromyography; Humans; Lipid Metabolism; Lipid Metabolism, Inborn Errors | 1985 |
Muscle carnitine deficiency. Association with lipid myopathy, vacuolar neuropathy, and vacuolated leukocytes.
Topics: Atrophy; Biological Transport; Carnitine; Electromyography; Female; Humans; Leukocytes; Lipid Metabo | 1974 |
Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome.
Topics: Acyltransferases; Adult; Carbon Isotopes; Carnitine; Coenzyme A Ligases; Fatty Acids; Female; Humans | 1973 |