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Anemia

Free Subscription Articles published in Am J Hematol Retrieve available abstracts of 140 articles: HTML format Text format

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December 2011
1. AYGUN B , Wruck LM, Schultz WH, Mueller BU, et al
   Chronic transfusion practices for prevention of primary stroke in children with sickle cell anemia and abnormal TCD velocities.
   Am J Hematol. 2011 Dec 29. doi: 10.1002/ajh.23105.
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2. SUN CC , Vaja V, Babitt JL, Lin HY, et al
   Targeting the hepcidin-ferroportin axis to develop new treatment strategies for anemia of chronic disease and anemia of inflammation.
   Am J Hematol. 2011 Dec 29. doi: 10.1002/ajh.23110.
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3. DAMPIER CD , Smith WR, Kim HY, Wager CG, et al
   Opioid patient controlled analgesia use during the initial experience with the IMPROVE PCA trial: a phase III analgesic trial for hospitalized sickle cell patients with painful episodes.
   Am J Hematol. 2011;86:E70-3.
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4. BAO W , Zhong H, Li X, Lee MT, et al
   Immune regulation in chronically transfused allo-antibody responder and nonresponder patients with sickle cell disease and beta-thalassemia major.
   Am J Hematol. 2011;86:1001-6.
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   November 2011
5. HENRY DH , Dahl NV, Auerbach MA
   Thrombocytosis and venous thromboembolism in cancer patients with chemotherapy induced anemia may be related to ESA induced iron restricted erythropoiesis and reversed by administration of IV iron.
   Am J Hematol. 2011 Nov 23. doi: 10.1002/ajh.22262.
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6. GILMORE A , Cho G, Howard J, Layton M, et al
   Feasibility and benefit of hydroxycarbamide as a long-term treatment for sickle cell disease patients: results from the North West London Sickle Cell Disease Registry.
   Am J Hematol. 2011;86:958-61.
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   October 2011
7. SAINI N , Jacobson JO, Jha S, Saini V, et al
   The perils of not digging deep enough-uncovering a rare cause of acquired anemia.
   Am J Hematol. 2011 Oct 23. doi: 10.1002/ajh.22235.
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8. KWIATKOWSKI JL , Cohen AR, Garro J, Alvarez O, et al
   Transfusional iron overload in children with sickle cell anemia on chronic transfusion therapy for secondary stroke prevention.
   Am J Hematol. 2011 Oct 20. doi: 10.1002/ajh.22228.
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9. KAMEL S , Lu Z, Sikaris K
   Comment on: Neutropenia and anemia with reduced serum vitamin B(12).
   Am J Hematol. 2011 Oct 20. doi: 10.1002/ajh.22226.
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10. AKINSHEYE I , Solovieff N, Ngo D, Malek A, et al
    Fetal hemoglobin in sickle cell anemia: Molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.
    Am J Hematol. 2011 Oct 14. doi: 10.1002/ajh.22221.
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11. AUERBACH M , Pappadakis JA, Bahrain H, Auerbach SA, et al
    Safety and efficacy of rapidly administered (one hour) one gram of low molecular weight iron dextran (INFeD) for the treatment of iron deficient anemia.
    Am J Hematol. 2011;86:860-2.
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12. RITHO J , Liu H, Hartzema AG, Lottenberg R, et al
    Hydroxyurea use in patients with sickle cell disease in a Medicaid population.
    Am J Hematol. 2011;86:888-90.
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13. ALI SB , Moosang M, King L, Knight-Madden J, et al
    Stroke recurrence in children with sickle cell disease treated with hydroxyurea following first clinical stroke.
    Am J Hematol. 2011;86:846-50.
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14. FUNG EB , Aguilar C, Micaily I, Haines D, et al
    Treatment of vitamin D deficiency in transfusion-dependent thalassemia.
    Am J Hematol. 2011;86:871-3.
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15. RIDER NL , Strauss KA, Brown K, Finkenstedt A, et al
    Erythrocyte pyruvate kinase deficiency in an old-order Amish cohort: longitudinal risk and disease management.
    Am J Hematol. 2011;86:827-34.
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16. HEMKER BG , Brousseau DC, Yan K, Hoffmann RG, et al
    When children with sickle-cell disease become adults: lack of outpatient care leads to increased use of the emergency department.
    Am J Hematol. 2011;86:863-5.
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    September 2011
17. BERMUDEZ A , Perez-Vazquez G, Insunza A, Baro J, et al
    FLAGIDA-lite is an effective regimen for patients between 70 and 80 years with acute myeloid leukemia or refractory anemia with excess blasts-2 and is feasible as outpatient treatment.
    Am J Hematol. 2011 Sep 21. doi: 10.1002/ajh.22192.
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18. CRARY SE , Ramaciotti C, Buchanan GR
    Prevalence of pulmonary hypertension in hereditary spherocytosis.
    Am J Hematol. 2011 Sep 7. doi: 10.1002/ajh.22182.
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19. AZZARA A , Carulli G, Galimberti S, Barate C, et al
    High-dose (40,000 IU twice/week) alpha recombinant human erythropoietin as single agent in low/intermediate risk myelodysplastic syndromes: A retrospective investigation on 133 patients treated in a single institution.
    Am J Hematol. 2011;86:762-7.
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20. PIGA A , Serra M, Longo F, Forni G, et al
    Changing patterns of splenectomy in transfusion-dependent thalassemia patients.
    Am J Hematol. 2011;86:808-10.
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21. MAHADEO KM , Oyeku S, Taragin B, Rajpathak SN, et al
    Increased prevalence of osteonecrosis of the femoral head in children and adolescents with sickle-cell disease.
    Am J Hematol. 2011;86:806-8.
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22. BOOTH KK , Terrell DR, Vesely SK, George JN, et al
    Systemic infections mimicking thrombotic thrombocytopenic purpura.
    Am J Hematol. 2011;86:743-51.
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23. RUSSO R , Gambale A, Esposito MR, Serra ML, et al
    Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.
    Am J Hematol. 2011;86:727-32.
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24. BRANDOW AM , Panepinto JA
    Monitoring toxicity, impact, and adherence of hydroxyurea in children with sickle cell disease.
    Am J Hematol. 2011;86:804-6.
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25. COHEN RT , Madadi A, Blinder MA, DeBaun MR, et al
    Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.
    Am J Hematol. 2011;86:756-61.
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26. GUINDO A , Traore K, Diakite S, Wellems TE, et al
    An evaluation of concurrent G6PD (A-) deficiency and sickle cell trait in Malian populations of children with severe or uncomplicated P. falciparum malaria.
    Am J Hematol. 2011;86:795-6.
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27. XUE F , Wentworth C, Ganesh V, Gastanaga V, et al
    Renal impairment, hemoglobinuria, and hemoglobinemia among patients with idiopathic thrombocytopenic purpura.
    Am J Hematol. 2011;86:738-42.
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    August 2011
28. LESESVE JF
    Mushroom-shaped red blood cells in protein band-3 deficiency.
    Am J Hematol. 2011;86:694.
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29. MINNITI CP , Taylor JG 6th, Hildesheim M, O'Neal P, et al
    Laboratory and echocardiography markers in sickle cell patients with leg ulcers.
    Am J Hematol. 2011;86:705-8.
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30. TSO AC , Roper DR, Wong CL, Bain B, et al
    Splenic infarction in a patient with sickle cell trait and hereditary spherocytosis.
    Am J Hematol. 2011;86:695-6.
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    July 2011
31. BHARADWAJ V , Chakravorty S, Bain BJ
    The cause of sudden anemia revealed by the blood film.
    Am J Hematol. 2011 Jul 29. doi: 10.1002/ajh.22158.
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32. WOOD SM , Meyers CA, Faderl S, Kantarjian HM, et al
    Association of anemia and cognitive dysfunction in patients with acute myelogenous leukemia and myelodysplastic syndrome.
    Am J Hematol. 2011 Jul 25. doi: 10.1002/ajh.22151.
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33. COLUCCI G , Silzle T, Solenthaler M
    Pyrazinamide-induced sideroblastic anemia.
    Am J Hematol. 2011 Jul 8. doi: 10.1002/ajh.22125.
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34. SUNDARAM N , Bennett M, Wilhelm J, Kim MO, et al
    Biomarkers for early detection of sickle nephropathy.
    Am J Hematol. 2011;86:559-66.
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35. UAPRASERT N , Rojnuckarin P, Settapiboon R, Amornsiriwat S, et al
    Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional alpha+ -thalassemia.
    Am J Hematol. 2011;86:615-7.
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    June 2011
36. SKIKNE BS , Punnonen K, Caldron PH, Bennett MT, et al
    Improved differential diagnosis of anemia of chronic disease and iron deficiency anemia: A prospective multicenter evaluation of soluble transferrin receptor and the sTfR/log ferritin index.
    Am J Hematol. 2011 Jun 14. doi: 10.1002/ajh.22108.
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37. SOBOTA A , Neufeld EJ, Sprinz P, Heeney MM, et al
    Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers.
    Am J Hematol. 2011;86:512-5.
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38. NUR E , Biemond BJ, Otten HM, Brandjes DP, et al
    Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management.
    Am J Hematol. 2011;86:484-9.
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    May 2011
39. LEE PL , Reid TJ 3rd, Bottomley SS, Barton JC, et al
    Sideroblastic anemia, iron overload, and ALAS2 R452S in African-American males: Phenotype and genotype features of five unrelated patients.
    Am J Hematol. 2011 May 31. doi: 10.1002/ajh.22088.
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40. LEBENSBURGER J , Johnson SM, Askenazi DJ, Rozario NL, et al
    Protective role of hemoglobin and fetal hemoglobin in early kidney disease for children with sickle cell anemia.
    Am J Hematol. 2011;86:430-2.
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41. KRISHNA R , O'Donovan E, Bain BJ
    Neutropenia and anemia with reduced serum vitamin B(12).
    Am J Hematol. 2011;86:417.
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42. TRACHTENBERG F , Vichinsky E, Haines D, Pakbaz Z, et al
    Iron chelation adherence to deferoxamine and deferasirox in thalassemia.
    Am J Hematol. 2011;86:433-6.
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43. SAVAGE WJ , Barron-Casella E, Fu Z, Dulloor P, et al
    Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
    Am J Hematol. 2011;86:427-9.
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44. DURAIRAJ S , Chew S, Hyslop A, Keenan N, et al
    Predicted costs of iron-chelators in myelodysplastic syndromes: a 10-year analysis based on actual prevalence and red cell transfusion rates.
    Am J Hematol. 2011;86:406-10.
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    April 2011
45. CASTILLO JJ , Sinclair N, Stachurski D, Jacobsen ED, et al
    Positive HIV ELISA test, autoimmune hemolytic anemia, and generalized lymphadenopathy: A unifying diagnosis.
    Am J Hematol. 2011 Apr 7. doi: 10.1002/ajh.22049.
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46. GREENWAY A , Ware RE, Thornburg CD
    Long-term results using hydroxyurea/phlebotomy for reducing secondary stroke risk in children with sickle cell anemia and iron overload.
    Am J Hematol. 2011;86:357-61.
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47. PARDANANI A , Begna K, Finke C, Lasho T, et al
    Circulating levels of MCP-1, sIL-2R, IL-15, and IL-8 predict anemia response to pomalidomide therapy in myelofibrosis.
    Am J Hematol. 2011;86:343-5.
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48. MCCAVIT TL , Lin H, Zhang S, Ahn C, et al
    Hospital volume, hospital teaching status, patient socioeconomic status, and outcomes in patients hospitalized with sickle cell disease.
    Am J Hematol. 2011;86:377-80.
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49. PADATE B , Bain BJ, de la Fuente J
    Ineffective hemopoietic in beta thalassemia major visualised.
    Am J Hematol. 2011;86:372.
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    March 2011
50. ALSULTAN A , Solovieff N, Aleem A, Algahtani FH, et al
    Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans.
    Am J Hematol. 2011 Mar 21. doi: 10.1002/ajh.22032.
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51. MALCOVATI L , Cazzola M
    The relevance of transfusion-dependency in the prognostic assessment of patients with myeloid neoplasms.
    Am J Hematol. 2011;86:241-3.
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52. CANDRILLI SD , O'Brien SH, Ware RE, Nahata MC, et al
    Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease.
    Am J Hematol. 2011;86:273-7.
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53. MILLER ST , Milton J, Steinberg MH
    G6PD deficiency and stroke in the CSSCD.
    Am J Hematol. 2011;86:331.
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54. ROSSI P , Curiel M, Demoux AL, Bagneres D, et al
    Bone marrow necrosis and sickle cell crisis associated with double heterozygosity for HbS and HbOARAB.
    Am J Hematol. 2011;86:309-10.
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    February 2011
55. SADAT-ALI M , Al-Elq A, Al-Turki H, Sultan O, et al
    Vitamin D level among patients with sickle cell anemia and its influence on bone mass.
    Am J Hematol. 2011 Feb 11. doi: 10.1002/ajh.22010.
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56. DWORKIS DA , Klings ES, Solovieff N, Li G, et al
    Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1.
    Am J Hematol. 2011;86:220-3.
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57. ECKMAN JR , Embury SH
    Sickle cell anemia pathophysiology: Back to the data.
    Am J Hematol. 2011;86:121-2.
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58. DAMPIER C , LeBeau P, Rhee S, Lieff S, et al
    Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.
    Am J Hematol. 2011;86:203-5.
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59. VASSEUR C , Pissard S, Domingues-Hamdi E, Marden MC, et al
    Evaluation of the free alpha-hemoglobin pool in red blood cells: a new test providing a scale of beta-thalassemia severity.
    Am J Hematol. 2011;86:199-202.
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60. ABDULSALAM AH , Sabeeh N, Bain BJ
    Diagnosis of beta thalassemia major from bone marrow morphology.
    Am J Hematol. 2011;86:187.
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61. LV L , Lin G, Gao X, Wu C, et al
    Case-control study of risk factors of myelodysplastic syndromes according to World Health Organization classification in a Chinese population.
    Am J Hematol. 2011;86:163-9.
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62. AWANDARE GA , Kempaiah P, Ochiel DO, Piazza P, et al
    Mechanisms of erythropoiesis inhibition by malarial pigment and malaria-induced proinflammatory mediators in an in vitro model.
    Am J Hematol. 2011;86:155-62.
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63. HEBBEL RP
    Reconstructing sickle cell disease: A data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.
    Am J Hematol. 2011;86:123-54.
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    January 2011
64. D'ANGELO G , Hotz AM
    Myelophthisis in breast cancer.
    Am J Hematol. 2011;86:70-1.
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65. GYANG E , Yeom K, Hoppe C, Partap S, et al
    Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease.
    Am J Hematol. 2011;86:104-6.
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66. HAYWOOD C JR , Beach MC, Bediako S, Carroll CP, et al
    Examining the characteristics and beliefs of hydroxyurea users and nonusers among adults with sickle cell disease.
    Am J Hematol. 2011;86:85-7.
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67. SEKERES MA , O'Keefe C, List AF, Paulic K, et al
    Demonstration of additional benefit in adding lenalidomide to azacitidine in patients with higher-risk myelodysplastic syndromes.
    Am J Hematol. 2011;86:102-3.
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68. BANYATSUPPASIN W , Butthep P, Atichartakarn V, Thakkinstian A, et al
    Activation of mononuclear phagocytes and its relationship to asplenia and phosphatidylserine exposing red blood cells in hemoglobin E/beta-thalassemia patients.
    Am J Hematol. 2011;86:89-92.
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69. SOBOTA A , Yamashita R, Xu Y, Trachtenberg F, et al
    Quality of life in thalassemia: a comparison of SF-36 results from the thalassemia longitudinal cohort to reported literature and the US norms.
    Am J Hematol. 2011;86:92-5.
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70. TREADWELL M , Telfair J, Gibson RW, Johnson S, et al
    Transition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.
    Am J Hematol. 2011;86:116-20.
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71. DE MONTALEMBERT M , Ferster A, Colombatti R, Rees DC, et al
    ENERCA clinical recommendations for disease management and prevention of complications of sickle cell disease in children.
    Am J Hematol. 2011;86:72-5.
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72. JERRELL JM , Tripathi A, Stallworth JR
    Pain management in children and adolescents with sickle cell disease.
    Am J Hematol. 2011;86:82-4.
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    December 2010
73. DANCHAIVIJITR P , Yared J, Rapoport AP
    Successful treatment of IgG and complement-mediated autoimmune hemolytic anemia with bortezomib and low-dose cyclophosphamide.
    Am J Hematol. 2010 Dec 2. doi: 10.1002/ajh.21950.
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74. CARRARA P , Balocco M, Pinto V, Olcese F, et al
    Manual erythroexchange for chronic transfusion therapy in patients with sickle cell syndromes unresponsive to hydroxyurea: a long-term follow-up.
    Am J Hematol. 2010;85:974.
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75. RENELLA R
    Progress in the congenital dyserythropoietic anemias: juicy but high-hanging fruits?
    Am J Hematol. 2010;85:913-4.
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76. PRITCHARD CC , Tait JF, Buller-Burckle AM, Mikula M, et al
    Annotation error of a common beta degrees -thalassemia mutation (619 bp-deletion) has implications for molecular diagnosis.
    Am J Hematol. 2010;85:978.
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77. PRESCOTT HC , Wu HM, Cataland SR, Baiocchi RA, et al
    Eculizumab therapy in an adult with plasma exchange-refractory atypical hemolytic uremic syndrome.
    Am J Hematol. 2010;85:976-7.
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    November 2010
78. HESS G , Nordyke RJ, Hill J, Hulnick S, et al
    Effect of reimbursement changes on erythropoiesis-stimulating agent utilization and transfusions.
    Am J Hematol. 2010;85:838-43.
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79. GOODNOUGH LT , Shander AS
    Erythropoiesis stimulating agents, blood transfusion, and the practice of medicine.
    Am J Hematol. 2010;85:835-7.
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80. NUR E , Mairuhu W, Biemond BJ, van Zanten AP, et al
    Urinary markers of bone resorption, pyridinoline and deoxypyridinoline, are increased in sickle cell patients with further increments during painful crisis.
    Am J Hematol. 2010;85:902-4.
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81. TERRELL DR , Vesely SK, Hovinga JA, Lammle B, et al
    Different disparities of gender and race among the thrombotic thrombocytopenic purpura and hemolytic-uremic syndromes.
    Am J Hematol. 2010;85:844-7.
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    October 2010
82. DIVAKARAN V , Mehta S, Yao D, Hassan S, et al
    Hepcidin in anemia of chronic heart failure.
    Am J Hematol. 2010.
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83. MINNITI CP , Eckman J, Sebastiani P, Steinberg MH, et al
    Leg ulcers in sickle cell disease.
    Am J Hematol. 2010;85:831-3.
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84. NASIMUZZAMAN M , Khandros E, Wang X, Kong Y, et al
    Analysis of alpha hemoglobin stabilizing protein overexpression in murine beta-thalassemia.
    Am J Hematol. 2010;85:820-2.
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85. VAN DEN TWEEL XW , van der Lee JH, Heijboer H, Peters M, et al
    Development and validation of a pediatric severity index for sickle cell patients.
    Am J Hematol. 2010;85:746-51.
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86. MEDNICK L , Yu S, Trachtenberg F, Xu Y, et al
    Symptoms of depression and anxiety in patients with thalassemia: prevalence and correlates in the thalassemia longitudinal cohort.
    Am J Hematol. 2010;85:802-5.
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87. WOOD JC , Glynos T, Thompson A, Giardina P, et al
    Follow-up report on the 2-year cardiac data from a deferasirox monotherapy trial.
    Am J Hematol. 2010;85:818-9.
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88. HEAD CA , Swerdlow P, McDade WA, Joshi RM, et al
    Beneficial effects of nitric oxide breathing in adult patients with sickle cell crisis.
    Am J Hematol. 2010;85:800-2.
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89. LANZKRON S , Carroll CP, Haywood C Jr
    The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.
    Am J Hematol. 2010;85:797-9.
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90. INATI A , Khoriaty E, Musallam KM, Taher AT, et al
    Iron chelation therapy for patients with sickle cell disease and iron overload.
    Am J Hematol. 2010;85:782-6.
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91. JELKMANN W
    Biosimilar epoetins and other "follow-on" biologics: update on the European experiences.
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92. STALLWORTH JR , Jerrell JM, Tripathi A
    Cost-effectiveness of hydroxyurea in reducing the frequency of pain episodes and hospitalization in pediatric sickle cell disease.
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93. DEL MONTE L , Manfredi R, Olivieri O, De Franceschi L, et al
    Sickle-cell-related acute abdominal painful crisis complicating the clinical management of a cocaine-packer.
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    September 2010
94. RUSSO R , Esposito MR, Asci R, Gambale A, et al
    Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene.
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    August 2010
95. CHEUNG AT , Miller JW, Craig SM, To PL, et al
    Comparison of real-time microvascular abnormalities in pediatric and adult sickle cell anemia patients.
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96. NARESH KN , Pavlu J
    Plasmacytoid dendritic cell nodules in bone marrow biopsies of chronic myelomonocytic leukemia.
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97. GUASCH A
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98. BRANDOW AM , Jirovec DL, Panepinto JA
    Hydroxyurea in children with sickle cell disease: practice patterns and barriers to utilization.
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99. FRAQUELLI M , Cassinerio E, Roghi A, Rigamonti C, et al
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100. HILLMEN P , Elebute M, Kelly R, Urbano-Ispizua A, et al
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     July 2010
101. SHMUKLER BE , Kedar PS, Warang P, Desai M, et al
     Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
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102. VAN TUIJN CF , van Beers EJ, Schnog JJ, Biemond BJ, et al
     Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease.
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103. ZANOTTI R , Frattini F, Ghia P, Visco C, et al
     ZAP-70 expression is associated with increased risk of autoimmune cytopenias in CLL patients.
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     June 2010
104. LIEM RI , Young LT, Lay AS, Pelligra SA, et al
     Reproducibility of tricuspid regurgitant jet velocity measurements in children and young adults with sickle cell disease undergoing screening for pulmonary hypertension.
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105. AUERBACH M , Silberstein PT, Webb RT, Averyanova S, et al
     Darbepoetin alfa 300 or 500 mug once every 3 weeks with or without intravenous Iron in patients with chemotherapy-induced anemia.
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106. STEINBERG MH , McCarthy WF, Castro O, Ballas SK, et al
     The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5 year follow-up.
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107. BALOCCO M , Carrara P, Pinto V, Forni GL, et al
     Daily alternating deferasirox and deferiprone therapy for "hard-to-chelate" beta-thalassemia major patients.
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108. AGOSTONI P , Salvioni E, Debenedetti C, Vignati C, et al
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109. ATWEH GF
     Hydroxyurea in sickle cell disease: What will it take to change practice?
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110. CARMEL R , Bellevue R, Kelman Z
     Low cobalamin levels associated with sickle cell disease: Contrasting origins and clinical meanings in two instructive patients.
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     May 2010
111. WANG Z , Yan H, Zhu L, Wang H, et al
     Successful unmanipulated stem cell transplantation from HLA-haploidentical 3-loci-mismatched parents in two children with severe aplastic anemia not responding to immunosuppressive therapy.
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112. FARRA C , Zahed L, Nietert PJ, Hourani H, et al
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113. LIU J , Jia X, Tang N, Wang L, et al
     A comprehensive, simple molecular assay of common deletions and mutations causing alpha-thalassemia in Southeast Asia and southern China.
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114. PRABHAKAR H , Haywood C Jr, Molokie R
     Sickle cell disease in the United States: looking back and forward at 100 years of progress in management and survival.
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115. TRACHTENBERG F , Foote D, Martin M, Carson S, et al
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116. BALAGULA Y , Newman SB, Lacouture ME
     Photodermatosis associated with eculizumab (Soliris): a novel monoclonal antibody directed against the complement protein C5.
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117. LU M , Cohen MH, Rieves D, Pazdur R, et al
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     April 2010
118. BALLAS SK , Bauserman RL, McCarthy WF, Castro OL, et al
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119. BAIN BJ
     A ghostly presence-G6PD deficiency.
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120. VAN TUIJN CF , Nur E, van Beers EJ, Zaaijer HL, et al
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121. TAHER AT , Musallam KM, Wood JC, Cappellini MD, et al
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     March 2010
122. NARESH KN , Marks AJ
     Peripheral blood and bone marrow morphology in adult T-cell leukaemia/lymphoma.
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123. RAYBURG M , Kalinyak KA, Towbin AJ, Baker PB, et al
     Fatal bone marrow embolism in a child with hemoglobin SE disease.
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     February 2010
124. COYNE DW , Auerbach M
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125. SESSA R , Puzone S, Ammirabile M, Piscopo C, et al
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126. MESA RA , Pardanani AD, Hussein K, Wu W, et al
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127. BAIN BJ , Thompson EM
     Expression of CD117 by proerythroblasts.
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     January 2010
128. BAIN BJ , Lee L
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129. BAIN BJ
     Schistocytes in megaloblastic anemia.
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130. DAVENPORT GC , Ouma C, Hittner JB, Were T, et al
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131. KAMBLE S , Telen MJ, Dinan MA, Grussemeyer CA, et al
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132. BROUSSEAU DC , Panepinto JA, Nimmer M, Hoffmann RG, et al
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133. FITZHUGH CD , Lauder N, Jonassaint JC, Telen MJ, et al
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134. DEBAUN MR
     Finally, a consensus statement on sickle cell disease manifestations: a critical step in improving the medical care and research agenda for individuals with sickle cell disease.
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135. SOLOVEY A , Kollander R, Milbauer LC, Abdulla F, et al
     Endothelial nitric oxide synthase and nitric oxide regulate endothelial tissue factor expression in vivo in the sickle transgenic mouse.
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136. SOBOTA A , Graham DA, Heeney MM, Neufeld EJ, et al
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137. BALLAS SK , Lieff S, Benjamin LJ, Dampier CD, et al
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138. KHALIQUE Z , Pavlu J, Lefroy D, Layton M, et al
     Erythrocytapheresis in the prevention of recurrent myocardial infarction in sickle cell disease.
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139. BAIN BJ , Riches J
     Help with HELLP.
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     December 2009
140. FIELD JJ , Madadi AR, Siegel MJ, Narra V, et al
     Author response letter to: "Pulmonary thrombi are not detected by 3D magnetic resonance angiography in adults with sickle cell anemia and an elevated tricuspid regurgitant jet velocity"
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