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Results: 1-8 |
Results: 8
DEFECTIVE BILIRUBIN CONJUGATION IN G-6-PD DEFICIENT NEONATES
Authors: KAPLAN M RUBALTELLI FF HAMMERMAN C VILEI MT LEITER C ABRAMOV A MURACA M
Citation: M. Kaplan et al., DEFECTIVE BILIRUBIN CONJUGATION IN G-6-PD DEFICIENT NEONATES, Pediatric research, 39(4), 1996, pp. 1306-1306
CONJUGATED BILIRUBIN IN NEONATES WITH GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY
Authors: KAPLAN M RUBALTELLI FF HAMMERMAN C VILEI MT LEITER C ABRAMOV A MURACA M
Citation: M. Kaplan et al., CONJUGATED BILIRUBIN IN NEONATES WITH GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY, The Journal of pediatrics, 128(5), 1996, pp. 695-697
CONTRIBUTION OF HEMOLYSIS TO JAUNDICE IN SEPHARDIC JEWISH GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENT NEONATES
Authors: KAPLAN M VREMAN HJ HAMMERMAN C LEITER C ABRAMOV A STEVENSON DK
Citation: M. Kaplan et al., CONTRIBUTION OF HEMOLYSIS TO JAUNDICE IN SEPHARDIC JEWISH GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENT NEONATES, British Journal of Haematology, 93(4), 1996, pp. 822-827
NEONATAL SCREENING FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G-6-PD) DEFICIENCY - SEX DISTRIBUTION AND ROLE OF PATERNITY
Authors: KAPLAN M HAMMERMAN C ABRAMOV A
Citation: M. Kaplan et al., NEONATAL SCREENING FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G-6-PD) DEFICIENCY - SEX DISTRIBUTION AND ROLE OF PATERNITY, Pediatric research, 36(1), 1994, pp. 10000020-10000020
NEONATAL SCREENING FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY -SEX DISTRIBUTION
Authors: KAPLAN M HAMMERMAN C KVIT R RUDENSKY B ABRAMOV A
Citation: M. Kaplan et al., NEONATAL SCREENING FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY -SEX DISTRIBUTION, Archives of Disease in Childhood, 71(1), 1994, pp. 60000059-60000060
DIVERSITY OF BETA-GLOBIN MUTATIONS IN ISRAELI ETHNIC-GROUPS REFLECTS RECENT HISTORIC EVENTS
Authors: FILON D ORON V KRICHEVSKI S SHAAG A SHAAG Y WARREN TC GOLDFARB A SHNEOR Y KOREN A AKER M ABRAMOV A RACHMILEWITZ EA RUND D KAZAZIAN HH OPPENHEIM A
Citation: D. Filon et al., DIVERSITY OF BETA-GLOBIN MUTATIONS IN ISRAELI ETHNIC-GROUPS REFLECTS RECENT HISTORIC EVENTS, American journal of human genetics, 54(5), 1994, pp. 836-843
A LIFELONG HYPERCOAGULABLE STATE IN BETA-THALASSEMIA MAJOR IS ASSOCIATED WITH IN-VIVO PLATELET ACTIVATION, PROTEIN-C AND PROTEIN-S DEFICIENCY AND ENHANCED ERYTHROCYTE PROCOAGULANT ACTIVITY AND AGGREGATION
Authors: ELDOR A MACLOUF J DURST R HYAM E GOLDFARB A RACHMILEWITZ EA ABRAMOV A BENYASHAR V BARENHOLZ Y DERAUCOURT E GUILLIN MC CHEN S GAVISH B YEDGAR S
Citation: A. Eldor et al., A LIFELONG HYPERCOAGULABLE STATE IN BETA-THALASSEMIA MAJOR IS ASSOCIATED WITH IN-VIVO PLATELET ACTIVATION, PROTEIN-C AND PROTEIN-S DEFICIENCY AND ENHANCED ERYTHROCYTE PROCOAGULANT ACTIVITY AND AGGREGATION, Thrombosis and haemostasis, 69(6), 1993, pp. 968-968
SILENT CARRIER BETA-THALASSEMIA DUE TO A SEVERE BETA-GLOBIN MUTATION INTERACTING WITH OTHER GENETIC ELEMENTS
Authors: RUND D FILON D OPPENHEIM A ABRAMOV A
Citation: D. Rund et al., SILENT CARRIER BETA-THALASSEMIA DUE TO A SEVERE BETA-GLOBIN MUTATION INTERACTING WITH OTHER GENETIC ELEMENTS, European journal of pediatrics, 152(7), 1993, pp. 574-576
Risultati: 1-8 |