phenylalanine has been researched along with Proteinuria in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (57.14) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hashimoto, H; Kanai, Y; Sugimoto, K; Tsuda, H; Yamaji, K; Yang, KS | 1 |
Hall, JE; Price, CC; Seed, JR | 1 |
Fällström, SP; Lindblad, B; Steen, G | 1 |
Beck, M; Bökenkamp, A; Lentze, MJ; Liappis, N | 1 |
Hjalmarson, O; Holme, E; Lindstedt, S; Lock, EA; Strandvik, B | 1 |
Matsukura, H; Naiki, S; Okada, T; Sakuragawa, N; Suzuki, Y | 1 |
Century, B; Natelson, S; Vorkink, WP | 1 |
7 other study(ies) available for phenylalanine and Proteinuria
Article | Year |
---|---|
Immunoadsorption plasmapheresis using a phenylalanine column as an effective treatment for lupus nephritis.
Topics: Adult; Analysis of Variance; Antibodies, Antinuclear; Complement System Proteins; Creatinine; Female; Heparin; Humans; Lupus Nephritis; Male; Phenylalanine; Plasmapheresis; Prednisolone; Proteinuria; Retrospective Studies; Treatment Outcome | 2006 |
A physiological mechanism to explain pathogenesis in African trypanosomiasis.
Topics: Animals; Arvicolinae; Creatinine; Humans; Ketoglutaric Acids; Phenylalanine; Phenylpyruvic Acids; Proteinuria; Pyruvates; Pyruvic Acid; Trypanosoma brucei brucei; Trypanosomiasis, African | 1983 |
On the renal tubular damage in hereditary tyrosinemia and on the formation of succinylacetoacetate and succinylacetone.
Topics: Acetoacetates; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Heptanoates; Homogentisic Acid; Humans; Infant; Keto Acids; Kidney Diseases; Kidney Tubules; Male; Phenylalanine; Proteinuria; Tyrosine | 1981 |
Effect of storage on phenylalanine and tyrosine measurements in whole-blood samples.
Topics: Adolescent; Blood Specimen Collection; Child; Child, Preschool; Humans; Infant; Phenylalanine; Proteinuria; Time Factors; Tyrosine | 2001 |
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Acetoacetates; alpha-Fetoproteins; Amino Acid Metabolism, Inborn Errors; Aminolevulinic Acid; Child; Child, Preschool; Cyclohexanones; Erythrocytes; Heptanoates; Humans; Hydroxybenzoates; Infant; Kidney Tubules; Liver; Nitrobenzoates; Phenylalanine; Phosphates; Porphobilinogen Synthase; Proteinuria; Tyrosine | 1992 |
Automated separation and measurement of urinary isoenzymes and protein by ion-exchange liquid chromatography.
Topics: Alkaline Phosphatase; Animals; Child; Chromatography, Ion Exchange; gamma-Glutamyltransferase; Homoarginine; Humans; Indicators and Reagents; Isoenzymes; Kidney; L-Lactate Dehydrogenase; Phenylalanine; Proteinuria; Rabbits; Species Specificity | 1987 |
Thin-layer chromatographic screening of amino acids in plasma and urine of newborns.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Blood Proteins; Chromatography, Thin Layer; Female; Glycine; Homocysteine; Humans; Indicators and Reagents; Infant, Newborn; Infant, Premature; Lysine; Methionine; Phenylalanine; Pregnancy; Proteinuria; Tyrosine; Ultrafiltration | 1974 |