transferrin has been researched along with Edema, Fetal in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lingappa, L; Panigrahy, N; Ramadevi, AR; Venkatlakshmi, A | 1 |
| Edwards, M; Fietz, M; Fletcher, J; McKenzie, F; O'callaghan, S; Somerset, D; Spilsbury, J; Woodford, P | 1 |
| den Hollander, NS; Lefeber, DJ; Matthijs, G; Poorthuis, BJ; Ruijter, GJ; Steggerda, SJ; van de Kamp, JM; Wevers, RA; Willems, SM | 1 |
3 other study(ies) available for transferrin and Edema, Fetal
| Article | Year |
|---|---|
Congenital Disorder of Glycosylation (CDG) Presenting as Non-immune Hydrops Fetalis.
Topics: Congenital Disorders of Glycosylation; Fatal Outcome; Female; Glycosylation; Humans; Hydrops Fetalis; Infant, Newborn; Isoelectric Focusing; Phosphotransferases (Phosphomutases); Transferrin | 2016 |
Prenatal diagnosis of congenital disorder of glycosylation type Ia (CDG-Ia) by cordocentesis and transferrin isoelectric focussing of serum of a 27-week fetus with non-immune hydrops.
Topics: Abnormalities, Multiple; Adult; Carbohydrate Metabolism, Inborn Errors; Cordocentesis; Female; Fetal Death; Glycosylation; Humans; Hydrops Fetalis; Isoelectric Focusing; Phosphotransferases (Phosphomutases); Prenatal Diagnosis; Transferrin | 2006 |
Congenital disorder of glycosylation type Ia presenting with hydrops fetalis.
Topics: Abnormalities, Multiple; Codon, Nonsense; Fatal Outcome; Female; Ferritins; Frameshift Mutation; Glycoproteins; Glycosylation; Heart Defects, Congenital; Humans; Hydrops Fetalis; Hypoalbuminemia; Infant, Newborn; Isoelectric Focusing; Male; Mutagenesis, Insertional; Mutation, Missense; Pericardial Effusion; Phosphotransferases (Phosphomutases); Protein Processing, Post-Translational; Thrombocytopenia; Transferrin; Ultrasonography, Prenatal | 2007 |