carnitine has been researched along with Embryopathies in 9 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "No further seizures were noted by day 5." | 5.51 | A newborn with seizures born to a mother diagnosed with primary carnitine deficiency. ( Chen, S; Hu, Y; Huang, Y; Lin, J; Lin, Z; Nan, Y; Zhou, X, 2019) |
| "No further seizures were noted by day 5." | 1.51 | A newborn with seizures born to a mother diagnosed with primary carnitine deficiency. ( Chen, S; Hu, Y; Huang, Y; Lin, J; Lin, Z; Nan, Y; Zhou, X, 2019) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (33.33) | 18.2507 |
| 2000's | 5 (55.56) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, S | 2 |
| Hu, Y | 1 |
| Huang, Y | 1 |
| Nan, Y | 1 |
| Zhou, X | 1 |
| Lin, J | 1 |
| Lin, Z | 1 |
| Walter, JH | 1 |
| Patterson, A | 1 |
| Till, J | 1 |
| Besley, GT | 1 |
| Fleming, G | 1 |
| Henderson, MJ | 1 |
| Hasegawa, Y | 1 |
| Iga, M | 1 |
| Kimura, M | 1 |
| Shigematsu, Y | 2 |
| Yamaguchi, S | 1 |
| Christodoulou, J | 1 |
| Teo, SH | 1 |
| Hammond, J | 1 |
| Sim, KG | 1 |
| Hsu, BY | 1 |
| Stanley, CA | 2 |
| Watson, B | 1 |
| Lau, KC | 1 |
| Wilcken, B | 1 |
| Chalmers, RA | 1 |
| English, N | 1 |
| Wigglesworth, JS | 1 |
| Treem, WR | 1 |
| Braida, L | 1 |
| Crovella, S | 1 |
| Boniotto, M | 1 |
| Luchesi, A | 1 |
| de Vonderweid, U | 1 |
| Casetta, B | 1 |
| Amoroso, A | 1 |
| Chisholm, CA | 1 |
| Vavelidis, F | 1 |
| Lovell, MA | 1 |
| Sweetman, L | 1 |
| Roe, CR | 1 |
| Roe, DS | 1 |
| Frerman, FE | 1 |
| Wilson, WG | 1 |
| Kikawa, Y | 1 |
| Sudo, M | 1 |
| Kanaoka, H | 1 |
| Fujioka, M | 1 |
| Dan, M | 1 |
1 review available for carnitine and Embryopathies
| Article | Year |
|---|---|
New developments in the pathophysiology, clinical spectrum, and diagnosis of disorders of fatty acid oxidation.
Topics: Acetyl Coenzyme A; Carnitine; Fatty Acids; Female; Fetal Diseases; Humans; Infant; Lipid Metabolism, | 2000 |
8 other studies available for carnitine and Embryopathies
| Article | Year |
|---|---|
A newborn with seizures born to a mother diagnosed with primary carnitine deficiency.
Topics: Brain; Cardiomyopathies; Carnitine; Electroencephalography; Female; Fetal Diseases; Humans; Hyperamm | 2019 |
Bloodspot acylcarnitine and amino acid analysis in cord blood samples: efficacy and reference data from a large cohort study.
Topics: Amino Acids; Blood Chemical Analysis; Blood Specimen Collection; Carnitine; Cohort Studies; Efficien | 2009 |
Prenatal diagnosis for organic acid disorders using two mass spectrometric methods, gas chromatography mass spectrometry and tandem mass spectrometry.
Topics: Amniotic Fluid; Carboxylic Acids; Carnitine; Female; Fetal Diseases; Gas Chromatography-Mass Spectro | 2005 |
First prenatal diagnosis of the carnitine transporter defect.
Topics: Carnitine; Carnitine Acyltransferases; Chorionic Villi Sampling; Female; Fetal Diseases; Humans; Mal | 1996 |
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.
Topics: Adult; Amnion; Breast Feeding; Carnitine; Carnitine Acyltransferases; Carnitine O-Palmitoyltransfera | 1997 |
A rapid and quantitative mass spectrometry method for determining the concentration of acylcarnitines and aminoacids in amniotic fluid.
Topics: Amino Acids; Amniotic Fluid; Carnitine; Female; Fetal Diseases; Humans; Mass Spectrometry; Metabolic | 2001 |
Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated alpha-fetoprotein and cystic renal changes.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; alpha-Fetoproteins; Amniocentesis; Amniotic Fluid; | 2001 |
Prenatal diagnosis of isovaleric acidemia by fast atom bombardment and tandem mass spectrometry.
Topics: Amniotic Fluid; Carnitine; Female; Fetal Diseases; Glycine; Hemiterpenes; Humans; Isovaleryl-CoA Deh | 1991 |