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Results: 1-21 |
Results: 21
Universal newborn screening for Hb H disease in California
Authors: Lorey, F Cunningham, G Vichinsky, EP Lubin, BH Witkowska, HE Matsunaga, A Azimi, M Sherwin, J Eastman, J Farina, F Waye, JS Chui, DHK
Citation: F. Lorey et al., Universal newborn screening for Hb H disease in California, GENET TEST, 5(2), 2001, pp. 93-100
Transfusion therapy: A coming-of-age treatment for patients with sickle cell disease
Authors: Reed, W Vichinsky, EP
Citation: W. Reed et Ep. Vichinsky, Transfusion therapy: A coming-of-age treatment for patients with sickle cell disease, J PED H ONC, 23(4), 2001, pp. 197-202
Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial
Authors: Vichinsky, EP Luban, NLC Wright, E Olivieri, N Driscoll, C Pegelow, CH Adams, RJ
Citation: Ep. Vichinsky et al., Prospective RBC phenotype matching in a stroke-prevention trial in sickle cell anemia: a multicenter transfusion trial, TRANSFUSION, 41(9), 2001, pp. 1086-1092
Current issues with blood transfusions in sickle cell disease
Authors: Vichinsky, EP
Citation: Ep. Vichinsky, Current issues with blood transfusions in sickle cell disease, SEM HEMATOL, 38(1), 2001, pp. 14-22
Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease
Authors: Miller, ST Macklin, EA Pegelow, CH Kinney, TR Sleeper, LA Bello, JA DeWill, LD Gallagher, DM Guarini, L Moser, FG Obene-Frempong, K Sanchez, N Vichinsky, EP Wang, WC Wethers, DL Younkin, DP Zimmerman, RA DeBaun, MR
Citation: St. Miller et al., Silent infarction as a risk factor for overt stroke in children with sickle cell anemia: A report from the Cooperative Study of Sickle Cell Disease, J PEDIAT, 139(3), 2001, pp. 385-390
Correlation of abnormal intracranial vessel velocity, measured by transcranial Doppler ultrasonography, with abnormal conjunctival vessel velocity, measured by computer-assisted intravital microscopy, in sickle cell disease
Authors: Cheung, ATW Harmatz, P Wun, T Chen, PCY Larkin, EC Adams, RJ Vichinsky, EP
Citation: Atw. Cheung et al., Correlation of abnormal intracranial vessel velocity, measured by transcranial Doppler ultrasonography, with abnormal conjunctival vessel velocity, measured by computer-assisted intravital microscopy, in sickle cell disease, BLOOD, 97(11), 2001, pp. 3401-3404
Patterns of arginine and nitric oxide in patients with sickle cell diseasewith vaso-occlusive crisis and acute chest syndrome
Authors: Morris, CR Kuypers, FA Larkin, S Vichinsky, EP Styles, LA
Citation: Cr. Morris et al., Patterns of arginine and nitric oxide in patients with sickle cell diseasewith vaso-occlusive crisis and acute chest syndrome, J PED H ONC, 22(6), 2000, pp. 515-520
Changing outcome of homozygous alpha-thalassemia: Cautious optimism
Authors: Singer, ST Styles, L Bojanowski, J Quirolo, K Foote, D Vichinsky, EP
Citation: St. Singer et al., Changing outcome of homozygous alpha-thalassemia: Cautious optimism, J PED H ONC, 22(6), 2000, pp. 539-542
Report of proceedings: 1999 international conference on E-beta thalassemia
Authors: Vichinsky, EP
Citation: Ep. Vichinsky, Report of proceedings: 1999 international conference on E-beta thalassemia, J PED H ONC, 22(6), 2000, pp. 550-550
Multicenter comparison of magnetic resonance imaging and transcranial Doppler ultrasonography in the evaluation of the central nervous system in children with sickle cell disease
Authors: Wang, WC Gallagher, DM Pegelow, CH Wright, EC Vichinsky, EP Abboud, MR Moser, FG Adams, RJ
Citation: Wc. Wang et al., Multicenter comparison of magnetic resonance imaging and transcranial Doppler ultrasonography in the evaluation of the central nervous system in children with sickle cell disease, J PED H ONC, 22(4), 2000, pp. 335-339
Acute chest syndrome in sickle cell disease. Reply
Authors: Dean, D Neumayr, LD Vichinsky, EP
Citation: D. Dean et al., Acute chest syndrome in sickle cell disease. Reply, N ENG J MED, 343(18), 2000, pp. 1336-1337
Causes and outcomes of the acute chest syndrome in sickle cell disease.
Authors: Vichinsky, EP Neumayr, LD Earles, AN Williams, R Lennette, ET Dean, D Nickerson, B Orringer, E McKie, V Bellevue, R Daeschner, C Manci, EA
Citation: Ep. Vichinsky et al., Causes and outcomes of the acute chest syndrome in sickle cell disease., N ENG J MED, 342(25), 2000, pp. 1855-1865
Sickle-cell disease not identified by newborn screening because of prior transfusion
Authors: Reed, W Lane, PA Lorey, F Bojanowski, J Glass, M Louie, RR Lubin, BH Vichinsky, EP
Citation: W. Reed et al., Sickle-cell disease not identified by newborn screening because of prior transfusion, J PEDIAT, 136(2), 2000, pp. 248-250
Arginine therapy: a novel strategy to induce nitric oxide production in sickle cell disease
Authors: Morris, CR Kuypers, FA Larkin, S Sweeters, N Simon, J Vichinsky, EP Styles, LA
Citation: Cr. Morris et al., Arginine therapy: a novel strategy to induce nitric oxide production in sickle cell disease, BR J HAEM, 111(2), 2000, pp. 498-500
Secretory phospholipase A(2) predicts impending acute chest syndrome in sickle cell disease
Authors: Styles, LA Aarsman, AJ Vichinsky, EP Kuypers, FA
Citation: La. Styles et al., Secretory phospholipase A(2) predicts impending acute chest syndrome in sickle cell disease, BLOOD, 96(9), 2000, pp. 3276-3278
Alloimmunization and erythrocyte autoimmunization in transfusion-dependentthalassemia patients of predominantly Asian descent
Authors: Singer, ST Wu, V Mignacca, R Kuypers, FA Morel, P Vichinsky, EP
Citation: St. Singer et al., Alloimmunization and erythrocyte autoimmunization in transfusion-dependentthalassemia patients of predominantly Asian descent, BLOOD, 96(10), 2000, pp. 3369-3373
Erythrocytapheresis for chronically transfused children with sickle cell disease: An effective method for maintaining a low hemoglobin S level and reducing iron overload
Authors: Singer, ST Quirolo, K Nishi, K Hackney-Stephens, E Evans, C Vichinsky, EP
Citation: St. Singer et al., Erythrocytapheresis for chronically transfused children with sickle cell disease: An effective method for maintaining a low hemoglobin S level and reducing iron overload, J CLIN APH, 14(3), 1999, pp. 122-125
The perioperative complication rate of orthopedic surgery in sickle cell disease: Report of the national sickle cell surgery study group
Authors: Vichinsky, EP Neumayr, LD Haberkern, C Earles, AN Eckman, J Koshy, M Black, DM
Citation: Ep. Vichinsky et al., The perioperative complication rate of orthopedic surgery in sickle cell disease: Report of the national sickle cell surgery study group, AM J HEMAT, 62(3), 1999, pp. 129-138
Deferoxamine treatment during pregnancy: Is it harmful?
Authors: Singer, ST Vichinsky, EP
Citation: St. Singer et Ep. Vichinsky, Deferoxamine treatment during pregnancy: Is it harmful?, AM J HEMAT, 60(1), 1999, pp. 24-26
Bone disease in beta-thalassaemia
Authors: Singer, ST Vichinsky, EP
Citation: St. Singer et Ep. Vichinsky, Bone disease in beta-thalassaemia, LANCET, 354(9182), 1999, pp. 881-882
Silent cerebral infarcts in sickle cell anemia: A risk factor analysis
Authors: Kinney, TR Sleeper, LA Wang, WC Zimmerman, RA Pegelow, CH Ohene-Frempong, K Wethers, DL Bello, JA Vichinsky, EP Moser, FG Gallagher, DM DeBaun, MR Platt, OS Miller, ST
Citation: Tr. Kinney et al., Silent cerebral infarcts in sickle cell anemia: A risk factor analysis, PEDIATRICS, 103(3), 1999, pp. 640-645
Risultati: 1-21 |