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Results: 1-11 |
Results: 11
Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in childrenwith sickle cell anemia
Authors: Passon, RG Howard, TA Zimmerman, SA Schultz, WH Ware, RE
Citation: Rg. Passon et al., Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in childrenwith sickle cell anemia, J PED H ONC, 23(7), 2001, pp. 448-451
Hydroxyurea therapy for pediatric patients with hemoglobin SC disease
Authors: Miller, MK Zimmerman, SA Schultz, WH Ware, RE
Citation: Mk. Miller et al., Hydroxyurea therapy for pediatric patients with hemoglobin SC disease, J PED H ONC, 23(5), 2001, pp. 306-308
An infant with homozygous hemoglobin D-Iran
Authors: Thornburg, CD Zimmerman, SA Schultz, WH Ware, RE
Citation: Cd. Thornburg et al., An infant with homozygous hemoglobin D-Iran, J PED H ONC, 23(1), 2001, pp. 67-68
A procedure for multiple-pulse maximum permissible exposure determination under the Z136.1-2000 American National Standard for Safe Use of Lasers
Authors: Thomas, RJ Rockwell, BA Marshall, WJ Aldrich, RC Zimmerman, SA Rockwell, RJ
Citation: Rj. Thomas et al., A procedure for multiple-pulse maximum permissible exposure determination under the Z136.1-2000 American National Standard for Safe Use of Lasers, J LASER APP, 13(4), 2001, pp. 134-140
Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus
Authors: Higginbotham, EA Zimmerman, SA Howard, TA Schanberg, L Kredich, D Ware, RE
Citation: Ea. Higginbotham et al., Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus, J RHEUMATOL, 28(2), 2001, pp. 370-372
Genitourinary complications of sickle cell disease
Authors: Bruno, D Wigfall, DR Zimmerman, SA Rosoff, PM Wiener, JS
Citation: D. Bruno et al., Genitourinary complications of sickle cell disease, J UROL, 166(3), 2001, pp. 803-811
Palpable splenomegaly in children with haemoglobin SC disease: Haematological and clinical manifestations
Authors: Zimmerman, SA Ware, RE
Citation: Sa. Zimmerman et Re. Ware, Palpable splenomegaly in children with haemoglobin SC disease: Haematological and clinical manifestations, CLIN LAB H, 22(3), 2000, pp. 145-150
Hemoglobin S/O-ARAB: Thirteen new cases and review of the literature
Authors: Zimmerman, SA O'Branski, EE Rosse, WF Ware, RE
Citation: Sa. Zimmerman et al., Hemoglobin S/O-ARAB: Thirteen new cases and review of the literature, AM J HEMAT, 60(4), 1999, pp. 279-284
Disaffection, dissimulation, and the uncertain ground of silent dismission: Juxtaposing John Milton and Elizabeth Cary
Authors: Zimmerman, SA
Citation: Sa. Zimmerman, Disaffection, dissimulation, and the uncertain ground of silent dismission: Juxtaposing John Milton and Elizabeth Cary, ELH-ENGL L, 66(3), 1999, pp. 553-589
Erythrocyte autoantibodies in paediatric patients with sickle cell diseasereceiving transfusion therapy: frequency, characteristics and significance
Authors: Castellino, SM Combs, MR Zimmerman, SA Issitt, PD Ware, RE
Citation: Sm. Castellino et al., Erythrocyte autoantibodies in paediatric patients with sickle cell diseasereceiving transfusion therapy: frequency, characteristics and significance, BR J HAEM, 104(1), 1999, pp. 189-194
Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease
Authors: Ware, RE Zimmerman, SA Schultz, WH
Citation: Re. Ware et al., Hydroxyurea as an alternative to blood transfusions for the prevention of recurrent stroke in children with sickle cell disease, BLOOD, 94(9), 1999, pp. 3022-3026
Risultati: 1-11 |