carnitine has been researched along with Carboxylase Deficiency, Combined in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Larson, AA | 1 |
| Balasubramaniam, S | 1 |
| Christodoulou, J | 1 |
| Burrage, LC | 1 |
| Marom, R | 1 |
| Graham, BH | 1 |
| Diaz, GA | 1 |
| Glamuzina, E | 1 |
| Hauser, N | 1 |
| Heese, B | 1 |
| Horvath, G | 1 |
| Mattman, A | 1 |
| van Karnebeek, C | 1 |
| Lane Rutledge, S | 1 |
| Williamson, A | 1 |
| Estrella, L | 1 |
| Van Hove, JKL | 1 |
| Weisfeld-Adams, JD | 1 |
| Yokoi, K | 2 |
| Ito, T | 2 |
| Maeda, Y | 2 |
| Nakajima, Y | 2 |
| Kurono, Y | 2 |
| Sugiyama, N | 2 |
| Togari, H | 2 |
| Ohmi, H | 1 |
| Ueta, A | 1 |
3 other studies available for carnitine and Carboxylase Deficiency, Combined
| Article | Year |
|---|---|
Biochemical signatures mimicking multiple carboxylase deficiency in children with mutations in MT-ATP6.
Topics: Adolescent; Carnitine; Child; Child, Preschool; Cohort Studies; Female; Genetic Testing; Humans; Inf | 2019 |
A case of holocarboxylase synthetase deficiency with insufficient response to prenatal biotin therapy.
Topics: Acetylcarnitine; Biotin; Carnitine; Female; Holocarboxylase Synthetase Deficiency; Humans; Infant, N | 2009 |
Determination of 3-hydroxyisovalerylcarnitine and other acylcarnitine levels using liquid chromatography-tandem mass spectrometry in serum and urine of a patient with multiple carboxylase deficiency.
Topics: Carnitine; Chromatography, Liquid; Humans; Multiple Carboxylase Deficiency; Reproducibility of Resul | 2008 |