palmitoylcarnitine has been researched along with Hypoglycemia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ajihara, S; Asada, T; Awaya, T; Bo, R; Fujiki, R; Fukao, T; Hamada, Y; Hara, K; Hasegawa, Y; Hata, I; Ishige, M; Ishige, N; Kagawa, R; Kobayashi, H; Kobayashi, M; Kono, T; Maruyama, S; Musha, I; Naito, E; Noguchi, A; Ohara, O; Ohtake, A; Okada, S; Sakura, N; Sasai, H; Shigematsu, Y; Tajima, G; Takayanagi, M; Tsumura, M; Yamada, K; Yamaguchi, S | 1 |
| Aleck, K; Ding, JH; Grebe, TA; He, G; Roe, CR; Roe, DS; Teramoto, R; Yang, BZ | 1 |
2 other study(ies) available for palmitoylcarnitine and Hypoglycemia
| Article | Year |
|---|---|
Newborn screening for carnitine palmitoyltransferase II deficiency using (C16+C18:1)/C2: Evaluation of additional indices for adequate sensitivity and lower false-positivity.
Topics: Alleles; Carnitine O-Palmitoyltransferase; Dried Blood Spot Testing; False Negative Reactions; False Positive Reactions; Female; Humans; Hypoglycemia; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Neonatal Screening; Palmitoylcarnitine; Sensitivity and Specificity; Tandem Mass Spectrometry | 2017 |
Identification of two novel mutations in the hypoglycemic phenotype of very long chain acyl-CoA dehydrogenase deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Alleles; Carnitine; Child, Preschool; DNA, Complementary; Exons; Female; Fibroblasts; Humans; Hypoglycemia; Mitochondria; Mutation; Palmitoylcarnitine; Phenotype | 1999 |