carnitine has been researched along with Deficiency Disease, Ornithine Carbamoyltransferase in 5 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "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) |
| "Assay ornithine transcarbamylase deficiency had normal results." | 1.28 | An unusual presentation of medium-chain acyl coenzyme A dehydrogenase deficiency. ( Marsden, D; Nyhan, WL; Roschinger, W; Sege-Petersen, K; Sweetman, L, 1992) |
| "Carnitine status was evaluated in 12 patients with hyperammonemic attacks caused by a deficiency in ornithine transcarbamylase." | 1.27 | Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency. ( Matsuda, I; Ohtani, Y; Ohyanagi, K; Yamamoto, S, 1988) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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 |
| Romshe, CA | 1 |
| Hilty, MD | 1 |
| McClung, HJ | 1 |
| Kerzner, B | 1 |
| Reiner, CB | 1 |
| Marsden, D | 1 |
| Sege-Petersen, K | 1 |
| Nyhan, WL | 1 |
| Roschinger, W | 1 |
| Sweetman, L | 1 |
| Nagao, M | 1 |
| Tsuchiyama, A | 1 |
| Aoyama, T | 1 |
| Mori, T | 1 |
| Oyanagi, K | 1 |
| Ohtani, Y | 1 |
| Ohyanagi, K | 1 |
| Yamamoto, S | 1 |
| Matsuda, I | 1 |
5 other studies available for carnitine and Deficiency Disease, Ornithine Carbamoyltransferase
| Article | Year |
|---|---|
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 |
Amino acid pattern in Reye syndrome: comparison with clinically similar entities.
Topics: Amino Acids; Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing); Carnitine; Diagnosis, Differentia | 1981 |
An unusual presentation of medium-chain acyl coenzyme A dehydrogenase deficiency.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Carnitine; Fatty Acid Desaturases; Female | 1992 |
Secondary carnitine deficiency in the newborn period in twins of a mother with partial ornithine transcarbamylase deficiency.
Topics: Carnitine; Diseases in Twins; Female; Humans; Infant, Newborn; Ornithine Carbamoyltransferase Defici | 1989 |
Secondary carnitine deficiency in hyperammonemic attacks of ornithine transcarbamylase deficiency.
Topics: Ammonia; Carnitine; Child; Child, Preschool; Female; Humans; Infant, Newborn; Liver; Male; Ornithine | 1988 |