carnitine has been researched along with Lipidoses in 18 studies
Lipidoses: Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Since it is a treatable disorder, this diagnosis must be considered by performing an acylcarnitine profile in all patients presenting with an unexplained muscular weakness." | 3.76 | [Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis]. ( Acquaviva-Bourdain, C; Brivet, M; Eymard, B; Jardel, C; Laforêt, P; Lombès, A; Maillart, E; Rigal, O; Vianey-Saban, C, 2010) |
| "The acute lipidosis most probably is explained by a slow oxidation of 22:1 acyl-CoA by the mitochondrial acyl-CoA dehydrogenase combined with an inhibitory effect of this CoA ester on the oxidation of acyl-CoA esters of a more "normal" chain length." | 2.36 | Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet. ( Bremer, J; Norum, KR, 1982) |
| "Idiopathic hepatic lipidosis was diagnosed in 11 cats." | 1.28 | Treatment of idiopathic hepatic lipidosis in cats: 11 cases (1986-1987). ( Allen, S; Cornelius, L; Greene, C; Jacobs, G, 1989) |
| "Carnitine was decreased in the skeletal muscles and the serum." | 1.27 | Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathy. ( Hirata, K; Hirose, F; Kato, H; Matsuishi, T; Nonaka, I; Ohta, K; Ohtaki, E; Sugiyama, N; Terasawa, K; Yoshino, M, 1985) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (72.22) | 18.7374 |
| 1990's | 3 (16.67) | 18.2507 |
| 2000's | 1 (5.56) | 29.6817 |
| 2010's | 1 (5.56) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Maillart, E | 1 |
| Acquaviva-Bourdain, C | 1 |
| Rigal, O | 1 |
| Brivet, M | 1 |
| Jardel, C | 1 |
| Lombès, A | 1 |
| Eymard, B | 1 |
| Vianey-Saban, C | 1 |
| Laforêt, P | 1 |
| BALL, CR | 1 |
| Gilly, R | 1 |
| Carrier, H | 1 |
| Lamit, J | 1 |
| Armbrustmacher, VW | 1 |
| Griffin, JL | 1 |
| Bremer, J | 2 |
| Norum, KR | 1 |
| Nikaido, H | 1 |
| Horiuchi, M | 1 |
| Hashimoto, N | 1 |
| Saheki, T | 1 |
| Hayakawa, J | 1 |
| Cui, L | 1 |
| Tang, X | 1 |
| Zhang, Q | 1 |
| Li, B | 1 |
| Du, H | 1 |
| Guo, Y | 1 |
| Blanchard, G | 1 |
| Paragon, BM | 1 |
| Milliat, F | 1 |
| Lutton, C | 1 |
| Angelini, C | 1 |
| Morand, P | 1 |
| Despert, F | 1 |
| Carrier, HN | 1 |
| Saudubray, BM | 1 |
| Fardeau, M | 1 |
| Romieux, B | 1 |
| Fauchier, C | 1 |
| Combe, P | 1 |
| Jerusalem, F | 1 |
| Spiess, H | 1 |
| Baumgartner, G | 1 |
| Bradley, WG | 1 |
| Tomlinson, BE | 1 |
| Hardy, M | 1 |
| Branca, D | 1 |
| Scutari, G | 1 |
| Siliprandi, N | 1 |
| Jacobs, G | 2 |
| Cornelius, L | 2 |
| Keene, B | 1 |
| Rakich, P | 1 |
| Shug, A | 1 |
| Allen, S | 1 |
| Greene, C | 1 |
| Hokland, B | 1 |
| Arredondo, M | 1 |
| Ramos, R | 1 |
| Hernández, M | 1 |
| López, S | 1 |
| Trujillo, R | 1 |
| Matsuishi, T | 1 |
| Hirata, K | 1 |
| Terasawa, K | 1 |
| Kato, H | 1 |
| Yoshino, M | 1 |
| Ohtaki, E | 1 |
| Hirose, F | 1 |
| Nonaka, I | 1 |
| Sugiyama, N | 1 |
| Ohta, K | 1 |
3 reviews available for carnitine and Lipidoses
| Article | Year |
|---|---|
Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet.
Topics: Acyl Coenzyme A; Adaptation, Physiological; Animals; Cardiomyopathies; Carnitine; Carnitine Acyltran | 1982 |
Lipid storage myopathies. A review of metabolic defect and of treatment.
Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Female; Humans; Infant; | 1976 |
Role of carnitine-dependent metabolic pathways in heart disease without primary ischemia.
Topics: Amino Acids, Branched-Chain; Animals; Cardiomyopathies; Carnitine; Fatty Acids; Kidney; Lipidoses; L | 1987 |
15 other studies available for carnitine and Lipidoses
| Article | Year |
|---|---|
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis].
Topics: Acyl-CoA Dehydrogenases; Adult; Biopsy; Brain Diseases, Metabolic; Carnitine; Coloring Agents; DNA M | 2010 |
ACTIONS OF BETAINE, CARNITINE AND CHOLINE ON THE PATTERN OF HEPATIC LIPOSIS IN MICE FED A HIGH-FAT, LOW-PROTEIN DIET.
Topics: Animals; Betaine; Carnitine; Choline; Diet, High-Fat; Diet, Protein-Restricted; Dietary Fats; Dietar | 1964 |
[Congenital myopathy with lipid and glycogen overload of muscle fiber and partial deficit of carnitine].
Topics: Carnitine; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Lipidoses; Mal | 1980 |
Pathology of inflammatory and metabolic myopathies.
Topics: AMP Deaminase; Carnitine; Carnitine O-Palmitoyltransferase; Glycogen Storage Disease; Humans; Lipido | 1981 |
Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on chromosome 11.
Topics: Animals; Carnitine; Chromosome Mapping; Chromosomes; Crosses, Genetic; DNA; Genes, Recessive; Lipido | 1995 |
EMG study in the diagnosis and differential diagnosis of lipid storage myopathy.
Topics: Adolescent; Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child; Child, Preschool; Dermatomyos | 1998 |
Dietary L-carnitine supplementation in obese cats alters carnitine metabolism and decreases ketosis during fasting and induced hepatic lipidosis.
Topics: 3-Hydroxybutyric Acid; Animals; Carnitine; Cat Diseases; Cats; Dietary Supplements; Fasting; Fatty A | 2002 |
[Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment].
Topics: Biopsy; Cardiomyopathies; Carnitine; Child; Female; Follow-Up Studies; Humans; Lipid Metabolism; Lip | 1979 |
Lipid storage myopathy with normal carnitine levels.
Topics: Acetyltransferases; Acid Phosphatase; Adenosine Triphosphatases; Adult; Carnitine; Electromyography; | 1975 |
Further studies of mitochondrial and lipid storage myopathies.
Topics: Adolescent; Adult; Brain; Carnitine; Female; Humans; Lipidoses; Male; Middle Aged; Mitochondria, Mus | 1978 |
Carnitine effect on heart steatosis induced in rats by rapeseed oil.
Topics: Animals; Cardiomyopathies; Carnitine; Cholesterol; Dietary Fats; Erucic Acids; Fatty Acids; Lipidose | 1977 |
Comparison of plasma, liver, and skeletal muscle carnitine concentrations in cats with idiopathic hepatic lipidosis and in healthy cats.
Topics: Animals; Carnitine; Cat Diseases; Cats; Female; Lipidoses; Liver; Liver Diseases; Male; Muscles; Mus | 1990 |
Treatment of idiopathic hepatic lipidosis in cats: 11 cases (1986-1987).
Topics: Animals; Carnitine; Cat Diseases; Cats; Enteral Nutrition; Female; Gastrostomy; Lipidoses; Liver Dis | 1989 |
[Systemic deficiency of carnitine].
Topics: Biopsy; Carnitine; Female; Humans; Infant; Lipidoses; Liver | 1987 |
Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathy.
Topics: Cardiomyopathies; Carnitine; Child; Child, Preschool; Humans; Lipidoses; Male; Muscles; Muscular Dis | 1985 |