transferrin has been researched along with BH4 Deficiency in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (40.00) | 18.7374 |
1990's | 2 (40.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Margeli, A; Papassotiriou, I; Papastamataki, M; Schulpis, KH; Stamou, H | 1 |
Datta, S; Gajra, B; Giri, AK; Roychaudhury, A; Sharma, A; Talukder, G | 1 |
Diels, M; Dotremont, H; François, B; Gillis, P | 1 |
Miranda da Cruz, BD; Seidler, H; Widhalm, K | 1 |
Easterberg, S; Farquhar, J; Hsia, DY; Kim, CB; Shih, LY; Yeh, S; Young, A | 1 |
5 other study(ies) available for transferrin and BH4 Deficiency
Article | Year |
---|---|
The effect of diet on total antioxidant status, ceruloplasmin, transferrin and ferritin serum levels in phenylketonuric children.
Topics: Antioxidants; Blood Cell Count; Ceruloplasmin; Copper; Diet; Erythrocyte Indices; Ferritins; Humans; Lipids; Lipoproteins; Oxidative Stress; Phenylalanine; Phenylketonurias; Transferrin | 2010 |
Some genetic markers in tribals of Eastern India.
Topics: Adult; Blood Group Antigens; Blood Proteins; Ethnicity; Female; Genetic Markers; Haptoglobins; Hemoglobins; Humans; India; L-Lactate Dehydrogenase; Lipoproteins; Male; Middle Aged; Phenylketonurias; Polymorphism, Genetic; Transferrin | 1982 |
Nutritional value of essential amino acids in the treatment of adults with phenylketonuria.
Topics: Adolescent; Adult; Amino Acids, Essential; Blood Proteins; Blood Urea Nitrogen; Creatinine; Feces; Humans; Nitrogen; Phenylketonurias; Serum Albumin; Transaminases; Transferrin | 1995 |
Iron status and iron supplementation in children with classical phenylketonuria.
Topics: Child; Child, Preschool; Diet; Erythrocyte Indices; Female; Ferritins; Hematocrit; Hemoglobins; Humans; Infant; Iron; Male; Phenylketonurias; Transferrin | 1993 |
The distribution of genetic polymorphisms among patients with Down's syndrome, phenylketonuria, and cystic fibrosis of the pancreas.
Topics: Acid Phosphatase; Adenine Nucleotides; Child; Cystic Fibrosis; Down Syndrome; Erythrocytes; Genes; Haptoglobins; Humans; Phenotype; Phenylketonurias; Phosphoglucomutase; Phosphogluconate Dehydrogenase; Phosphotransferases; Polymorphism, Genetic; Transferrin | 1969 |