carnitine has been researched along with Orphan Diseases in 6 studies
Orphan Diseases: Rare diseases that have not been well studied.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 5 (83.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Vanhoorne, V | 1 |
| Peeters, E | 1 |
| Van Tongelen, I | 1 |
| Boussery, K | 1 |
| Wynendaele, E | 1 |
| De Spiegeleer, B | 1 |
| Remon, JP | 1 |
| Vervaet, C | 1 |
| Işıkay, S | 1 |
| Qian, GL | 1 |
| Hong, F | 1 |
| Tong, F | 1 |
| Fu, HD | 1 |
| Liu, AM | 1 |
| Ogundare, O | 1 |
| Jumma, O | 1 |
| Turnbull, DM | 1 |
| Woywodt, A | 1 |
| Pierron, S | 1 |
| Giudicelli, H | 1 |
| Moreigne, M | 1 |
| Khalfi, A | 1 |
| Touati, G | 1 |
| Caruba, C | 1 |
| Rolland, MO | 1 |
| Acquaviva, C | 1 |
| Prada, CE | 1 |
| Jefferies, JL | 1 |
| Grenier, MA | 1 |
| Huth, CM | 1 |
| Page, KI | 1 |
| Spicer, RL | 1 |
| Towbin, JA | 1 |
| Leslie, ND | 1 |
1 review available for carnitine and Orphan Diseases
| Article | Year |
|---|---|
Recurrent rhabdomyolysis and glutaric aciduria type I: a case report and literature review.
Topics: Amino Acid Metabolism, Inborn Errors; Biopsy, Needle; Brain Diseases, Metabolic; Carnitine; Child, P | 2016 |
5 other studies available for carnitine and Orphan Diseases
| Article | Year |
|---|---|
Pharmaceutical compounding of orphan active ingredients in Belgium: how community and hospital pharmacists can address the needs of patients with rare diseases.
Topics: Arginine; Belgium; Carnitine; Drug Compounding; Excipients; Humans; Pharmacists; Phenylbutyrates; Pr | 2019 |
Cerebral multicystic lesions in a child with L-2 hydroxyglutaric aciduria: a rare disease and a rare association.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Carnitine; Central Nervous System Cysts; Child; Diagnosis, | 2014 |
Searching for the needle in the Haystacks.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Age of Onset; Biopsy; Carnitine; Creatine Kinase; Creatinine; Hi | 2009 |
[Late onset 3-HMG-CoA lyase deficiency: a rare but treatable disorder].
Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Chromosome Aberrations; | 2010 |
Malonyl coenzyme A decarboxylase deficiency: early dietary restriction and time course of cardiomyopathy.
Topics: Alleles; Carboxy-Lyases; Cardiomyopathies; Carnitine; Chromosome Aberrations; Chromosome Deletion; C | 2012 |