transferrin has been researched along with Classic Galactosemia in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 4 (44.44) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Asteggiano, CG; Azar, NB; Bistué Millón, MB; Dodelson de Kremer, R; Guelbert, N; Papazoglu, M; Peralta, MF; Pereyra, M; Spécola, NS; Suldrup, NS | 1 |
| Artuch, R; Briones, P; García-Villoria, J; Hernández-Pérez, JM; Montero, R; Navarro-Sastre, A; Quintana, E; Ribes, A | 1 |
| Barone, R; Fiumara, A; Garozzo, D; Jaeken, J; O'Brien, JF; Pavone, L; Perez, M; Sorge, G; Sturiale, L; Tortorelli, S; Zaffanello, M | 1 |
| Adamowicz, M; Kowalik, A; Pronicka, E; Płoski, R; Radomyska, B; Rogaszewska, M; Rokicki, D; Sykut-Cegielska, J | 1 |
| Berry, LR; Chindemi, PA; Hatton, MW; Regoeczi, E | 1 |
| Guthenberg, C; Kristiansson, B; Stibler, H; von Döbeln, U | 1 |
| Charlwood, J; Clayton, P; Keir, G; Mian, N; Winchester, B | 1 |
| Jaeken, J; Kint, J; Ramaekers, VT; Stibler, H | 1 |
| Gajewski, J; Laskowska-Klita, T; Szczypka, M; Zbieg-Sendecka, E | 1 |
1 trial(s) available for transferrin and Classic Galactosemia
| Article | Year |
|---|---|
Carbohydrate-deficient transferrin in galactosaemia.
Topics: Biomarkers; Child; Child, Preschool; Congenital Disorders of Glycosylation; Diagnosis, Differential; Female; Galactose; Galactosemias; Humans; Male; Reference Values; Transferrin | 1997 |
8 other study(ies) available for transferrin and Classic Galactosemia
| Article | Year |
|---|---|
Ten years of screening for congenital disorders of glycosylation in Argentina: case studies and pitfalls.
Topics: Adult; Argentina; Child; Child, Preschool; Collagen Type VI; Congenital Disorders of Glycosylation; Exome; Female; Galactosemias; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Glycolipids; Glycoproteins; Glycosylation; Homozygote; Humans; Infant; Infant, Newborn; Isoelectric Focusing; Male; Mass Screening; Neonatal Screening; Phenotype; Sequence Analysis, DNA; Transferrin | 2018 |
Screening for congenital disorders of glycosylation (CDG): transferrin HPLC versus isoelectric focusing (IEF).
Topics: Area Under Curve; Carbohydrate Metabolism, Inborn Errors; Case-Control Studies; Chromatography, High Pressure Liquid; Diet; Edetic Acid; Fructose Intolerance; Galactosemias; Glycosylation; Humans; Isoelectric Focusing; Mass Screening; Reference Values; Reproducibility of Results; Transferrin | 2009 |
Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.
Topics: Binding Sites; Chromatography, Liquid; Fucose; Galactose; Galactosemias; Glycolipids; Glycoproteins; Glycosylation; Humans; Hydrogen-Ion Concentration; Ions; Isoelectric Focusing; Male; Polysaccharides; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Temperature; Transferrin | 2005 |
Elevated carbohydrate-deficient transferrin (CDT) and its normalization on dietary treatment as a useful biochemical test for hereditary fructose intolerance and galactosemia.
Topics: Biomarkers; Child; Child, Preschool; Diet Therapy; Dietary Carbohydrates; Female; Fructose Intolerance; Galactosemias; Humans; Infant; Infant, Newborn; Male; Retrospective Studies; Transferrin | 2007 |
Galactose-specific elimination of human asialotransferrin by the bone marrow in the rabbit.
Topics: alpha-Fetoproteins; Animals; Asialoglycoproteins; Bone Marrow; Fetuins; Galactose; Galactosemias; Glycoproteins; Humans; Liver; Male; Orosomucoid; Rabbits; Transferrin | 1980 |
Defective galactosylation of serum transferrin in galactosemia.
Topics: Carbohydrate Sequence; Chromatography, High Pressure Liquid; Dietary Carbohydrates; Erythrocytes; Galactose; Galactosemias; Galactosephosphates; Glycosylation; Humans; Molecular Sequence Data; Molecular Structure; Polysaccharides; Transferrin; UDPglucose-Hexose-1-Phosphate Uridylyltransferase | 1998 |
A new variant of the carbohydrate deficient glycoproteins syndrome.
Topics: Carbohydrate Metabolism, Inborn Errors; Electromyography; Evoked Potentials; Female; Galactosemias; Glycoproteins; Hexosamines; Humans; Infant; Isoelectric Focusing; Liver; Magnetic Resonance Imaging; Mannose; Sialic Acids; Transferrin | 1991 |
Red blood cells and serum antioxidant defense systems of galactosaemic children.
Topics: Antioxidants; Cataract; Ceruloplasmin; Child; Child, Preschool; Erythrocytes; Galactosemias; Humans; Infant; Malondialdehyde; Oxidoreductases; Transferrin; Uric Acid | 1990 |