tyrosine has been researched along with Anemia, Hemolytic in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (71.43) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Defesche, JC; Hollak, CE; Holleboom, AG; Hovingh, GK; Kastelein, JJ; Kuivenhoven, JA; Levels, JH; Peter, J; Schimmel, AW; Stroes, ES; Valentijn, RM; van Olden, CC; Vos, P | 1 |
| Bedford, SJ; Bronson, RT; Dobarro, M; Ferris, S; Halperin, JA; Miranda, PV; Qin, X; Song, W; Visconti, PE | 1 |
| Goldberg, A; McColl, KE | 1 |
| Finegold, MJ | 1 |
| Bruckheimer, S; Burkert, LB; Pisciotta, AV; Ranney, HM; Sharma, VS | 1 |
| Sassa, S | 1 |
| Bradley, TB; Jacobs, A; Nagel, RL; Ranney, HM; Udem, L | 1 |
1 review(s) available for tyrosine and Anemia, Hemolytic
| Article | Year |
|---|---|
Cholestatic syndromes in infancy.
Topics: Anemia, Hemolytic; Bile; Bile Ducts; Cholestasis; Chromosome Aberrations; Chromosome Disorders; Fasting; Fructose Intolerance; Galactosemias; Histiocytosis, Langerhans-Cell; Humans; Infant; Infant, Newborn; Infections; Jaundice, Neonatal; Liver; Liver Cirrhosis; Niemann-Pick Diseases; Nutritional Physiological Phenomena; Syndrome; Tyrosine | 1976 |
6 other study(ies) available for tyrosine and Anemia, Hemolytic
| Article | Year |
|---|---|
Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
Topics: Adolescent; Anemia, Hemolytic; Angiotensin-Converting Enzyme Inhibitors; Animals; Child; Child, Preschool; Chlorocebus aethiops; Cholesterol, HDL; Corneal Opacity; COS Cells; Cysteine; Disulfides; Diuretics; Female; Genetic Predisposition to Disease; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Male; Mutation; Phosphatidylcholine-Sterol O-Acyltransferase; Proteinuria; Transfection; Treatment Outcome; Tyrosine | 2011 |
Further characterization of reproductive abnormalities in mCd59b knockout mice: a potential new function of mCd59 in male reproduction.
Topics: Anemia, Hemolytic; Animals; Apoptosis; CD59 Antigens; Complement C3; Complement C9; Complement Membrane Attack Complex; Female; In Vitro Techniques; Infertility, Male; Male; Mice; Mice, Knockout; Phosphorylation; Reproduction; Sperm Capacitation; Spermatozoa; Testis; Tyrosine | 2005 |
Abnormal porphyrin metabolism in diseases other than prophyria.
Topics: Alcohol Drinking; Amino Acid Metabolism, Inborn Errors; Anemia, Hemolytic; Anemia, Hypochromic; Anemia, Megaloblastic; Anemia, Sickle Cell; Anemia, Sideroblastic; Humans; Lead Poisoning; Leukemia; Liver Diseases; Malabsorption Syndromes; Mental Disorders; Polycythemia; Porphyrins; Time Factors; Tyrosine | 1980 |
Hemoglobin M equon beta 41 (C7) phenylalanine leads to tyrosine.
Topics: Adult; Amino Acids; Anemia, Hemolytic; Electrophoresis, Cellulose Acetate; Female; Hemoglobins, Abnormal; Humans; Methemoglobin; Oxygen Consumption; Peptides; Phenylalanine; Tyrosine; Wisconsin | 1976 |
[Significance of delta-aminolevulinic acid dehydratase analysis in clinical tests].
Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Hemolytic; Animals; Colorimetry; Erythrocytes; Fluorometry; Humans; Lead Poisoning; Porphobilinogen Synthase; Reference Values; Tyrosine | 1989 |
Hemoglobin L Ferrara in a Jewish family associated with a hemolytic state in the propositus.
Topics: Adult; Anemia, Hemolytic; Enzymes; Female; Genetics, Medical; Heinz Bodies; Hemoglobins, Abnormal; Heterozygote; Humans; Jews; Male; Pedigree; Tyrosine | 1969 |