carnitine has been researched along with Deficiency, Glucosephosphatase in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rossi, A | 1 |
| Ruoppolo, M | 1 |
| Formisano, P | 1 |
| Villani, G | 1 |
| Albano, L | 1 |
| Gallo, G | 1 |
| Crisci, D | 1 |
| Moccia, A | 1 |
| Parenti, G | 1 |
| Strisciuglio, P | 1 |
| Melis, D | 1 |
| Gilly, R | 1 |
| Carrier, H | 1 |
| Lamit, J | 1 |
| Holton, JB | 1 |
| Allen, JT | 1 |
| Green, CA | 1 |
| Partington, S | 1 |
| Gilbert, RE | 1 |
| Berry, PJ | 1 |
3 other studies available for carnitine and Deficiency, Glucosephosphatase
| Article | Year |
|---|---|
Insulin-resistance in glycogen storage disease type Ia: linking carbohydrates and mitochondria?
Topics: Acids; Adolescent; Adult; Antiporters; Biomarkers; Carnitine; Case-Control Studies; Child; Child, Pr | 2018 |
[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 |
Inherited metabolic diseases in the sudden infant death syndrome.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Carnitine; Child, Preschool; Female; Glycogen Stora | 1991 |