galactose has been researched along with Thrombopenia in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (42.86) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (28.57) | 24.3611 |
2020's | 2 (28.57) | 2.80 |
Authors | Studies |
---|---|
Abbonante, V; Balduini, A; Bastida, JM; Benito, R; Di Buduo, CA; Díaz-Ajenjo, L; García-Tuñón, I; González-Porras, JR; Hernández-Rivas, JM; Marín-Quílez, A; Miguel-García, C; Pardal, E; Peñarrubia, MJ; Rivera, J; Ruiz-Sala, P; Santos-Mínguez, S; Serramito-Gómez, I; Soprano, PM; Vuelta, E | 1 |
Balduini, A; Bastida, JM; Benito, R; Di Buduo, CA; Marín-Quílez, A; Rivera, J | 1 |
Ben-Harosh, M; Dgany, O; Doulatov, S; Gulsuner, S; King, MC; Krasnov, T; Pierce, S; Seo, A; Shalev, H; Shimamura, A; Tamary, H; Walsh, T | 1 |
Candotti, F; Kanegane, H; Morio, T; Motoyoshi, Y; Shimizu, M; Wada, T; Yachie, A | 1 |
Grainick, HR; Jenneau, C; Maisonneuve, P; McKeown, LP; Rick, ME; Sultan, Y; Williams, SB | 1 |
Dahr, W; Gunson, HH; Uhlenbruck, G; Van Der Hart, M | 1 |
Bisson, PG; Caldwell, RA; Hall, GH; Shaldon, C | 1 |
7 other study(ies) available for galactose and Thrombopenia
Article | Year |
---|---|
Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis.
Topics: Blood Platelets; Galactose; Glycosylation; Humans; Integrin beta1; Megakaryocytes; Thrombocytopenia; Thrombopoiesis; UDPglucose 4-Epimerase; Uridine Diphosphate | 2023 |
Topics: Galactose; Galactosemias; Hemorrhage; Humans; Thrombocytopenia; UDPglucose 4-Epimerase | 2023 |
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE).
Topics: Adult; Alleles; Exome Sequencing; Female; Galactose; Galactosemias; Gene Frequency; Humans; Male; Middle Aged; Pedigree; Thrombocytopenia; UDPglucose 4-Epimerase | 2019 |
Aberrant glycosylation of IgA in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Topics: Adolescent; Adult; Case-Control Studies; Child; Child, Preschool; Cohort Studies; Female; Galactose; Genetic Diseases, X-Linked; Glomerulonephritis; Glycosylation; Humans; Immunoglobulin A; Infant; Male; Retrospective Studies; Thrombocytopenia; Wiskott-Aldrich Syndrome; Young Adult | 2013 |
Von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor.
Topics: Antigens; Factor VIII; Fibrinogen; Galactose; Glycoproteins; Humans; Membrane Proteins; Platelet Aggregation; Platelet Membrane Glycoproteins; Ristocetin; Sialic Acids; Thrombocytopenia; von Willebrand Diseases; von Willebrand Factor | 1985 |
Molecular basis of Tn-polyagglutinability.
Topics: Anemia, Hemolytic; Antibodies, Heterophile; Blood Glucose; Blood Protein Electrophoresis; Cell Membrane; Chromatography, Gas; Electrophoresis, Polyacrylamide Gel; Erythrocytes; Glycopeptides; Hemagglutination; Hemagglutination Tests; Hexoses; Humans; Leukopenia; Molecular Weight; Sialic Acids; Sodium Dodecyl Sulfate; Syndrome; Thrombocytopenia; Trypsin | 1975 |
Heparin-treated haemolytic-uraemic syndrome simulating Fabry's disease.
Topics: Acute Kidney Injury; Anemia, Hemolytic; Child; Cholesterol; Chromatography, Thin Layer; Diagnosis, Differential; Glycolipids; Heparin; Hexoses; Humans; Kidney; Kidney Transplantation; Lipid Metabolism, Inborn Errors; Lipids; Male; Prednisone; Thrombocytopenia; Transplantation, Homologous | 1971 |