transferrin has been researched along with Acidosis, Lactic 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 | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fellman, V; Pihko, H; Raivio, KO; Rapola, J; Varilo, T | 1 |
Artigas, J; Briones, P; Chabás, A; Colomer, J; Ferrer, I; García-Silva, MT; Jaeken, J; Pineda, M; Vilaseca, MA | 1 |
2 other study(ies) available for transferrin and Acidosis, Lactic
Article | Year |
---|---|
Iron-overload disease in infants involving fetal growth retardation, lactic acidosis, liver haemosiderosis, and aminoaciduria.
Topics: Acidosis, Lactic; Female; Ferritins; Fetal Growth Retardation; Finland; Genes, Recessive; Hemosiderosis; Humans; Infant, Newborn; Iron Overload; Kidney; Liver; Male; Pedigree; Renal Aminoacidurias; Transferrin | 1998 |
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease.
Topics: Acidosis, Lactic; Adolescent; Adult; Child, Preschool; Consanguinity; Diagnosis, Differential; DNA Mutational Analysis; Female; Genetic Carrier Screening; Glycosylation; Humans; Leigh Disease; Male; Mitochondrial Encephalomyopathies; Phosphotransferases (Phosphomutases); Retinitis Pigmentosa; Spinocerebellar Degenerations; Transferrin | 2001 |