carnitine has been researched along with Vomiting in 14 studies
Vomiting: The forcible expulsion of the contents of the STOMACH through the MOUTH.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Our data suggest that a protocol consisting of mitochondrial-targeted cofactors (co-enzyme Q10 and L-carnitine) plus amitriptyline (or possibly cyproheptadine in preschoolers) coupled with blood level monitoring is highly effective in the prevention of vomiting episodes." | 7.77 | High degree of efficacy in the treatment of cyclic vomiting syndrome with combined co-enzyme Q10, L-carnitine and amitriptyline, a case series. ( Boles, RG, 2011) |
| "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) |
| "Our data suggest that a protocol consisting of mitochondrial-targeted cofactors (co-enzyme Q10 and L-carnitine) plus amitriptyline (or possibly cyproheptadine in preschoolers) coupled with blood level monitoring is highly effective in the prevention of vomiting episodes." | 3.77 | High degree of efficacy in the treatment of cyclic vomiting syndrome with combined co-enzyme Q10, L-carnitine and amitriptyline, a case series. ( Boles, RG, 2011) |
| "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) |
| "We report the first case of acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA in China." | 1.42 | [Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA]. ( Ding, Y; Li, X; Liu, Y; Song, J; Wang, H; Wang, Q; Wu, T; Yang, Y; Zhang, Y, 2015) |
| "N-carbamylglutamate is approved for the treatment of hyperammonemia in N-acetylglutamate synthetase deficiency and may have efficacy in other urea cycle disorders." | 1.39 | Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency. ( Bellantuono, R; Bellino, V; De Palo, T; Favia, V; Morrone, A; Papadia, F; Ranieri, A; Tummolo, A, 2013) |
| "Propionic acidemia is a hereditary metabolic disease caused by a deficiency of enzyme propionyl-CoA carboxylase, which is involved in the catabolism of ramified amino acids, odd-chain fatty acids, and other metabolites; the deficiency of this enzyme leads to an accumulation of toxic substances in the body." | 1.34 | Subacute presentation of propionic acidemia. ( de la Sierra García-Valdecasas, M; del Portal, LR; Delgado, C; Jiménez, LM; Macías, C; Pérez, M, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (21.43) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (35.71) | 29.6817 |
| 2010's | 5 (35.71) | 24.3611 |
| 2020's | 1 (7.14) | 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 |
| Tummolo, A | 1 |
| Favia, V | 1 |
| Bellantuono, R | 1 |
| Bellino, V | 1 |
| Ranieri, A | 1 |
| Morrone, A | 1 |
| De Palo, T | 1 |
| Papadia, F | 1 |
| Liu, Y | 1 |
| Wu, T | 1 |
| Wang, H | 1 |
| Ding, Y | 1 |
| Song, J | 1 |
| Li, X | 1 |
| Zhang, Y | 1 |
| Wang, Q | 1 |
| Yang, Y | 1 |
| Boles, RG | 1 |
| Listernick, R | 1 |
| Kumar, N | 1 |
| Bashar, Q | 1 |
| Reddy, N | 1 |
| Sengupta, J | 1 |
| Ananthakrishnan, A | 1 |
| Schroeder, A | 1 |
| Hogan, WJ | 1 |
| Venkatesan, T | 1 |
| Auré, K | 1 |
| Benoist, JF | 1 |
| Ogier de Baulny, H | 1 |
| Romero, NB | 1 |
| Rigal, O | 1 |
| Lombès, A | 1 |
| McLoughlin, LM | 1 |
| Trimble, ER | 1 |
| Jackson, P | 1 |
| Chong, SK | 1 |
| Delgado, C | 1 |
| Macías, C | 1 |
| de la Sierra García-Valdecasas, M | 1 |
| Pérez, M | 1 |
| del Portal, LR | 1 |
| Jiménez, LM | 1 |
| Van Calcar, SC | 1 |
| Harding, CO | 1 |
| Wolff, JA | 1 |
| Taubman, B | 1 |
| Hale, DE | 1 |
| Kelley, RI | 1 |
| Bressler, R | 1 |
| Corredor, C | 1 |
| Brendel, K | 1 |
| Tanaka, K | 1 |
| Miller, EM | 1 |
| Isselbacher, KJ | 1 |
1 review available for carnitine and Vomiting
| Article | Year |
|---|---|
Hypoglycin and hypoglycin-like compounds.
Topics: Amino Acids; Animals; Blood Glucose; Carnitine; Chemical Phenomena; Chemistry; Cholesterol; Coenzyme | 1969 |
13 other studies available for carnitine and Vomiting
| 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 |
Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency.
Topics: Adolescent; Arginine; Brain; Carnitine; Case Management; Citrulline; Coma; Combined Modality Therapy | 2013 |
[Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA].
Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases; Carnitine; Diet, Protein-Restricted; Hepatitis | 2015 |
High degree of efficacy in the treatment of cyclic vomiting syndrome with combined co-enzyme Q10, L-carnitine and amitriptyline, a case series.
Topics: Adolescent; Adrenergic Uptake Inhibitors; Adult; Amitriptyline; Carnitine; Child; Child, Preschool; | 2011 |
A 14-year-old boy with vomiting.
Topics: Abdominal Pain; Adolescent; Brain Ischemia; Carnitine; Cognition Disorders; Diagnosis, Differential; | 2012 |
Cyclic Vomiting Syndrome (CVS): is there a difference based on onset of symptoms--pediatric versus adult?
Topics: Adolescent; Adult; Age of Onset; Anticonvulsants; Antidepressive Agents, Tricyclic; Carnitine; Child | 2012 |
Progression despite replacement of a myopathic form of coenzyme Q10 defect.
Topics: Benzoquinones; Carnitine; Cerebellar Ataxia; Cerebellum; Child, Preschool; Disease Progression; Drug | 2004 |
L-carnitine in cyclical vomiting syndrome.
Topics: Antiemetics; Carnitine; Child; Humans; Male; Syndrome; Vomiting | 2004 |
L-carnitine.
Topics: Carnitine; Controlled Clinical Trials as Topic; Deficiency Diseases; Dietary Supplements; Double-Bli | 2004 |
Subacute presentation of propionic acidemia.
Topics: Acidosis; Amino Acids; Biotin; Brain; Carnitine; Diagnosis, Differential; Diet, Protein-Restricted; | 2007 |
L-carnitine administration reduces number of episodes in cyclic vomiting syndrome.
Topics: Adolescent; Carnitine; Child; Child, Preschool; Female; Humans; Infant; Male; Time Factors; Vomiting | 2002 |
Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase; Carboxylic Acids; Carnitine; Diagnosis, Differential; Fatty Acid Desaturases | 1987 |
Hypoglycin A: a specific inhibitor of isovaleryl CoA dehydrogenase.
Topics: Acidosis; Alanine; Amino Acid Metabolism, Inborn Errors; Animals; Butyrates; Caproates; Carbon Dioxi | 1971 |