carnitine has been researched along with Diseases in Twins in 10 studies
Diseases in Twins: Disorders affecting TWINS, one or both, at any age.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Infants with inborn errors of fatty acid metabolism may present with apnea, periodic breathing, and sudden infant death syndrome (SIDS)." | 7.69 | Familial infantile apnea and immature beta oxidation. ( Browning, IB; Iafolla, AK; Roe, CR, 1995) |
| "Fraternal twins who had fasting hypoglycemia, hypoketonemia, muscle weakness, and hepatic dysfunction are reported." | 5.27 | Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet. ( Bier, DM; Brown, BI; Dickie, M; Engel, AG; Glasgow, AM; Perry, LW; Todaro, J; Utter, MF, 1983) |
| "Infants with inborn errors of fatty acid metabolism may present with apnea, periodic breathing, and sudden infant death syndrome (SIDS)." | 3.69 | Familial infantile apnea and immature beta oxidation. ( Browning, IB; Iafolla, AK; Roe, CR, 1995) |
| "Barth syndrome is an X-linked recessive condition characterized by skeletal myopathy, cardiomyopathy, proportionate short stature, and recurrent neutropenia, but with normal cognitive function." | 1.29 | Barth syndrome: clinical observations and genetic linkage studies. ( Becker, LE; Bridge, PJ; Christodoulou, J; Clarke, JT; Jay, V; Lehotay, DC; McInnes, RR; Platt, BA; Robinson, BH; Wilson, G, 1994) |
| "Fraternal twins who had fasting hypoglycemia, hypoketonemia, muscle weakness, and hepatic dysfunction are reported." | 1.27 | Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet. ( Bier, DM; Brown, BI; Dickie, M; Engel, AG; Glasgow, AM; Perry, LW; Todaro, J; Utter, MF, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (40.00) | 18.7374 |
| 1990's | 4 (40.00) | 18.2507 |
| 2000's | 2 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dobrowolski, SF | 1 |
| McKinney, JT | 1 |
| Amat di San Filippo, C | 1 |
| Giak Sim, K | 1 |
| Wilcken, B | 1 |
| Longo, N | 1 |
| Halldin, MU | 1 |
| Forslund, A | 1 |
| von Döbeln, U | 1 |
| Eklund, C | 1 |
| Gustafsson, J | 1 |
| Glasgow, AM | 1 |
| Engel, AG | 1 |
| Bier, DM | 1 |
| Perry, LW | 1 |
| Dickie, M | 1 |
| Todaro, J | 1 |
| Brown, BI | 1 |
| Utter, MF | 1 |
| Salzer, H | 1 |
| Christodoulou, J | 1 |
| McInnes, RR | 1 |
| Jay, V | 1 |
| Wilson, G | 1 |
| Becker, LE | 1 |
| Lehotay, DC | 1 |
| Platt, BA | 1 |
| Bridge, PJ | 1 |
| Robinson, BH | 1 |
| Clarke, JT | 1 |
| Iafolla, AK | 1 |
| Browning, IB | 1 |
| Roe, CR | 1 |
| Fontaine, M | 1 |
| Briand, G | 1 |
| Ser, N | 1 |
| Armelin, I | 1 |
| Rolland, MO | 1 |
| Degand, P | 1 |
| Vamecq, J | 1 |
| Gibson, KM | 1 |
| Lee, CF | 1 |
| Wappner, RS | 1 |
| Nagao, M | 1 |
| Tsuchiyama, A | 1 |
| Aoyama, T | 1 |
| Mori, T | 1 |
| Oyanagi, K | 1 |
| Bressler, R | 1 |
1 review available for carnitine and Diseases in Twins
| Article | Year |
|---|---|
[New aspects in the diagnosis and therapy of fetal lung immaturity. Determination of the infant respiratory system compliance. Analysis of dipalmitoylphosphatidylcholine in amniotic fluid. Use of carnitine for the enhancement of lung maturation. (Clinical
Topics: Amniotic Fluid; Animals; Carnitine; Diseases in Twins; Fatty Acids; Female; Fetal Organ Maturity; Ge | 1982 |
9 other studies available for carnitine and Diseases in Twins
| Article | Year |
|---|---|
Validation of dye-binding/high-resolution thermal denaturation for the identification of mutations in the SLC22A5 gene.
Topics: Animals; Carnitine; Child; CHO Cells; Codon, Nonsense; Cricetinae; Cricetulus; Diseases in Twins; DN | 2005 |
Increased lipolysis in LCHAD deficiency.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Carnitine; Dicarboxylic Acids; Diseases in Twins; Energy Metabol | 2007 |
Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet.
Topics: Cardiomyopathies; Carnitine; Dietary Fats; Diseases in Twins; Female; Humans; Hypoglycemia; Infant; | 1983 |
Barth syndrome: clinical observations and genetic linkage studies.
Topics: Abnormalities, Multiple; Acids; Cardiomyopathy, Dilated; Carnitine; Diseases in Twins; Dwarfism; Ele | 1994 |
Familial infantile apnea and immature beta oxidation.
Topics: Apnea; Carnitine; Diseases in Twins; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, | 1995 |
Metabolic studies in twin brothers with 2-methylacetoacetyl-CoA thiolase deficiency.
Topics: Acetyl-CoA C-Acyltransferase; Acidosis; Biomarkers; Carnitine; Cells, Cultured; Child, Preschool; Di | 1996 |
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new case.
Topics: Carnitine; Diseases in Twins; Fibroblasts; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Lympho | 1992 |
Secondary carnitine deficiency in the newborn period in twins of a mother with partial ornithine transcarbamylase deficiency.
Topics: Carnitine; Diseases in Twins; Female; Humans; Infant, Newborn; Ornithine Carbamoyltransferase Defici | 1989 |
Carnitine and the twins.
Topics: Adolescent; Carnitine; Diseases in Twins; Fatty Acids; Female; Humans; Ligases; Lipid Metabolism, In | 1970 |