eosine yellowish-(ys) has been researched along with Anemia, Hemolytic, Congenital in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Agarwal, AM; Christensen, RD; Nussenzveig, RH; Prchal, JT; Yaish, HM | 1 |
Darbyshire, P; Dhermy, D; King, MJ; Langabeer, L; MacKinnon, H; McMahon, C; Telfer, P | 1 |
Behrens, J; Chambers, K; Flynn, C; Greenwood, D; King, MJ; Rogers, C | 1 |
3 other study(ies) available for eosine yellowish-(ys) and Anemia, Hemolytic, Congenital
Article | Year |
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Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis.
Topics: Anemia, Hemolytic, Congenital; Ankyrins; DNA Mutational Analysis; Eosine Yellowish-(YS); Flow Cytometry; Genetic Predisposition to Disease; Heredity; Heterozygote; Humans; Infant; Infant, Newborn; Jaundice, Neonatal; Jaundice, Obstructive; Male; Mutation; Osmotic Fragility; Pedigree; Phenotype; Predictive Value of Tests; Severity of Illness Index; Spectrin; Spherocytosis, Hereditary | 2014 |
Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Anemia, Hemolytic, Congenital; Child; Child, Preschool; Diagnosis, Differential; Eosine Yellowish-(YS); Erythrocyte Membrane; Erythrocytes, Abnormal; Female; Flow Cytometry; Humans; Infant; Male; Middle Aged; Spectrin; Spherocytosis, Hereditary | 2008 |
Rapid flow cytometric test for the diagnosis of membrane cytoskeleton-associated haemolytic anaemia.
Topics: Adult; Anemia, Hemolytic, Congenital; Anion Exchange Protein 1, Erythrocyte; Chymotrypsin; Cytoskeleton; Electrophoresis, Polyacrylamide Gel; Eosine Yellowish-(YS); Erythrocyte Membrane; Fetal Blood; Flow Cytometry; Fluorescent Dyes; Humans; Infant, Newborn; Predictive Value of Tests; ROC Curve; Spherocytosis, Hereditary | 2000 |