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Articles published in Haematologica

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    April 2008
  1. YOUNG NS , Kaufman DW
    The epidemiology of acquired aplastic anemia.
    Haematologica. 2008;93:489-92.
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  2. DOKAL I
    Fanconi anemia is a highly penetrant cancer susceptibility syndrome.
    Haematologica. 2008;93:486-8.
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    March 2008
  3. SPINOWITZ BS
    Anemia management in patients on peritoneal dialysis: efficacy and safety of epoetin {delta}
    Haematologica. 2008;.
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  4. MONTANE E , Ibanez L, Vidal X, Ballarin E, et al
    Epidemiology of aplastic anemia: a prospective multicenter study.
    Haematologica. 2008;.
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  5. ROSENBERG PS , Alter BP, Ebell W
    Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
    Haematologica. 2008;.
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    February 2008
  6. MALLORQUI J , Segura J, de Bolos C, Gutierrez-Gallego R, et al
    Recombinant erythropoietin found in seized blood bags from sportsmen.
    Haematologica. 2008;93:313-4.
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  7. LI W , Coates T, Wood JC
    Atrial dysfunction as a marker of iron cardiotoxicity in thalassemia major.
    Haematologica. 2008;93:311-2.
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  8. VAN BEERS EJ , Nieuwdorp M, Duits AJ, Evers LM, et al
    Sickle cell patients are characterized by a reduced glycocalyx volume.
    Haematologica. 2008;93:307-8.
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    January 2008
  9. GIRMENIA C , Pizzarelli G, Pozzi E, Cimino G, et al
    Improving outcomes of acute invasive Aspergillus rhinosinusitis in patients with hematologic malignancies or aplastic anemia: the role of voriconazole.
    Haematologica. 2008;93:159-60.
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  10. MITTAL S , Blaylock MG, Culligan DJ, Barker RN, et al
    A high rate of CLL phenotype lymphocytes in autoimmune hemolytic anemia and immune thrombocytopenic purpura.
    Haematologica. 2008;93:151-2.
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  11. CAMBERLEIN E , Zanninelli G, Detivaud L, Lizzi AR, et al
    Anemia in beta-thalassemia patients targets hepatic hepcidin transcript levels independently of iron metabolism genes controlling hepcidin expression.
    Haematologica. 2008;93:111-5.
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  12. SCHMITT-GRAEFF AH , Teo SS, Olschewski M, Schaub F, et al
    JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis.
    Haematologica. 2008;93:34-40.
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  13. UNEKE CJ , Iyare FE, Oke P, Duhlinska DD, et al
    Assessment of malaria in pregnancy using rapid diagnostic tests and its association with HIV infection and hematologic parameters in South-Eastern Nigeria.
    Haematologica. 2008;93:143-4.
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  14. LACERRA G , Scarano C, Musollino G, Flagiello A, et al
    Hb Foggia or alpha 117(GH5)Phe -> Ser: a new alpha 2 globin allele affecting the alpha Hb-AHSP interaction.
    Haematologica. 2008;93:141-2.
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  15. AU WY , Lam WW, Chu W, Tam S, et al
    A T2* magnetic resonance imaging study of pancreatic iron overload in thalassemia major.
    Haematologica. 2008;93:116-9.
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  16. HIROKAWA M , Sawada K, Fujishima N, Nakao S, et al
    Long-term response and outcome following immunosuppressive therapy in thymoma-associated pure red cell aplasia: a nationwide cohort study in Japan by the PRCA collaborative study group.
    Haematologica. 2008;93:27-33.
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  17. ATAGA KI , Moore CG, Hillery CA, Jones S, et al
    Coagulation activation and inflammation in sickle cell disease-associated pulmonary hypertension.
    Haematologica. 2008;93:20-6.
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  18. MALCOVATI L , Cazzola M
    Myelodysplastic/myeloproliferative disorders.
    Haematologica. 2008;93:4-6.
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  19. GLADWIN MT , Kato GJ
    Hemolysis-associated hypercoagulability in sickle cell disease: the plot (and blood) thickens!
    Haematologica. 2008;93:1-3.
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  20. MASERA N , Rescaldani C, Azzolini M, Vimercati C, et al
    Development of lens opacities with peculiar characteristics in patients affected by thalassemia major on chelating treatment with deferasirox (ICL670) at the Pediatric Clinic in Monza, Italy.
    Haematologica. 2008;93:e9-10.
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  21. AGUILA JD , Zamora MC, Fernandez OA, Jimenez LP, et al
    Comprehensive care for patients with sickle cell disease in Cuba.
    Haematologica. 2008;93:e20.
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  22. HADDAD AS , Subbiah V, Lichtin AE, Theil KS, et al
    Hypocupremia and bone marrow failure.
    Haematologica. 2008;93:e1-5.
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    December 2007
  23. OSUGI Y , Yagasaki H, Sako M, Kosaka Y, et al
    Antithymocyte globulin and cyclosporine for treatment of 44 children with hepatitis associated aplastic anemia.
    Haematologica. 2007;92:1687-1690.
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  24. PERCY MJ , Scott LM, Erber WN, Harrison CN, et al
    The frequency of JAK2 exon 12 mutations in idiopathic erythrocytosis patients with low serum erythropoietin levels.
    Haematologica. 2007;92:1607-14.
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  25. LINDEN T , Gerss J, Jurgens H
    The crux of the log rank test. Re: Locasciulli A, Oneto R, Bacigalupo A, Socie G, Korthof E, Bekassy A, Schrezenmeier H, Passweg J, Fuhrer M. Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunosuppress
    Haematologica. 2007;92:e122.
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  26. MANCO L , Goncalves P, Antunes P, Maduro F, et al
    Mutations and haplotype diversity in 70 Portuguese G6PD-deficient individuals: an overview on the origin and evolution of mutated alleles.
    Haematologica. 2007;92:1713-4.
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  27. DE MONTALEMBERT M , Aggoun Y, Niakate A, Szezepanski I, et al
    Endothelial-dependent vasodilation is impaired in children with sickle cell disease.
    Haematologica. 2007;92:1709-10.
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  28. PROVAN D , Butler T, Evangelista ML, Amadori S, et al
    Activity and safety profile of low-dose rituximab for the treatment of autoimmune cytopenias in adults.
    Haematologica. 2007;92:1695-8.
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  29. BADER-MEUNIER B , Aladjidi N, Bellmann F, Monpoux F, et al
    Rituximab therapy for childhood Evans syndrome.
    Haematologica. 2007;92:1691-4.
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  30. AYDINOK Y , Ulger Z, Nart D, Terzi A, et al
    A randomized controlled 1-year study of daily deferiprone plus twice weekly desferrioxamine compared with daily deferiprone monotherapy in patients with thalassemia major.
    Haematologica. 2007;92:1599-606.
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  31. BERENTSEN S
    Rituximab for the treatment of autoimmune cytopenias.
    Haematologica. 2007;92:1589-96.
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  32. NOIZAT-PIRENNE F , Bachir D, Chadebech P, Michel M, et al
    Rituximab for prevention of delayed hemolytic transfusion reaction in sickle cell disease.
    Haematologica. 2007;92:e132-5.
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    November 2007
  33. WANG Y , Yagasaki H, Hama A, Nishio N, et al
    Mutation of SBDS and SH2D1A is not associated with aplastic anemia in Japanese children.
    Haematologica. 2007;92:1573.
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  34. MANU PEREIRA M , Gelbart T, Ristoff E, Crain KC, et al
    Chronic non-spherocytic hemolytic anemia associated with severe neurological disease due to gamma-glutamylcysteine synthetase deficiency in a patient of Moroccan origin.
    Haematologica. 2007;92:e102-5.
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  35. LIEM RI , Young LT, Thompson AA
    Tricuspid regurgitant jet velocity is associated with hemolysis in children and young adults with sickle cell disease evaluated for pulmonary hypertension.
    Haematologica. 2007;92:1549-1552.
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  36. TSIRIGOTIS P , Sella T, Shapira MY, Bitan M, et al
    Peliosis hepatis following treatment with androgen-steroids in patients with bone marrow failure syndromes.
    Haematologica. 2007;92:e106-10.
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    October 2007
  37. HEIMPEL H , Kohne E, Schrod L, Schwarz K, et al
    A new type of transfusion-dependent congenital dyserythropoietic anemia.
    Haematologica. 2007;92:1427-8.
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  38. LOCATELLI F , Zecca M, Pession A, Morreale G, et al
    The outcome of children with Fanconi anemia given hematopoietic stem cell transplantation and the influence of fludarabine in the conditioning regimen: a report from the Italian pediatric group.
    Haematologica. 2007;92:1381-8.
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  39. DE FRANCESCHI L , Ronzoni L, Cappellini MD, Cimmino F, et al
    K-CL co-transport plays an important role in normal and beta thalassemic erythropoiesis.
    Haematologica. 2007;92:1319-26.
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  40. HUBACEK P , Maalouf J, Zajickova M, Kouba M, et al
    Failure of multiple antivirals to affect high HHV-6 DNAaemia resulting from viral chromosomal integration in case of severe aplastic anaemia.
    Haematologica. 2007;92:e98-e100.
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    September 2007
  41. LAHR G , Brintrup J, Over S, Feurle GE, et al
    Codon 104(-G), a dominant beta0-thalassemia-like phenotype in a German Caucasian family is associated with mild chronic hemolytic anemia but influenced in severity by co-inherited genetic factors.
    Haematologica. 2007;92:1264-5.
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  42. GUCHHAIT P , Dasgupta SK, Le A, Yellapragada S, et al
    Lactadherin mediates sickle cell adhesion to vascular endothelial cells in flowing blood.
    Haematologica. 2007;92:1266-7.
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    August 2007
  43. BOYD JH , Macklin EA, Strunk RC, Debaun MR, et al
    Asthma is associated with increased mortality in individuals with sickle cell anemia.
    Haematologica. 2007;92:1115-8.
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  44. ELIMELAKH M , Dayton V, Park KS, Gruessner AC, et al
    Red cell aplasia and autoimmune hemolytic anemia following immunosuppression with alemtuzumab, mycophenolate, and daclizumab in pancreas transplant recipients.
    Haematologica. 2007;92:1029-36.
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  45. MARRONE A , Sokhal P, Walne A, Beswick R, et al
    Functional characterization of novel telomerase RNA (TERC) mutations in patients with diverse clinical and pathological presentations.
    Haematologica. 2007;92:1013-20.
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  46. SAWADA K , Hirokawa M, Fujishima N, Teramura M, et al
    Long-term outcome of patients with acquired primary idiopathic pure red cell aplasia receiving cyclosporine A. A nationwide cohort study in Japan for the PRCA Collaborative Study Group.
    Haematologica. 2007;92:1021-8.
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  47. VALENTI L , Pulixi EA, Arosio P, Cremonesi L, et al
    Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.
    Haematologica. 2007;92:1037-1042.
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    July 2007
  48. HADAVI V , Taromchi AH, Malekpour M, Gholami B, et al
    Elucidating the spectrum of alpha-thalassemia mutations in Iran.
    Haematologica. 2007;92:992-3.
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  49. PAGANO L , Viola A, Fioretti G, Ammirabile M, et al
    Neapolis (CD 126 beta+ GGT->GGG): a result of a screening in Campania, a region in Southern Italy.
    Haematologica. 2007;92:990-1.
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  50. SWISHER KK , Doan JT, Vesely SK, Kwaan HC, et al
    Pancreatitis preceding acute episodes of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: report of five patients with a systematic review of published reports.
    Haematologica. 2007;92:936-43.
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  51. TELFER P , Coen P, Chakravorty S, Wilkey O, et al
    Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London.
    Haematologica. 2007;92:905-12.
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  52. MANNUCCI PM
    Thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome: much progress and many remaining issues.
    Haematologica. 2007;92:878-80.
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  53. ROBERTS I , de Montalembert M
    Sickle cell disease as a paradigm of immigration hematology: new challenges for hematologists in Europe.
    Haematologica. 2007;92:865-71.
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    June 2007
  54. KANNO H , Utsugisawa T, Aizawa S, Koizumi T, et al
    Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency.
    Haematologica. 2007;92:731-7.
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  55. ADEWOYE AH , Nolan V, McMahon L, Ma Q, et al
    Effectiveness of a dedicated day hospital for management of acute sickle cell pain.
    Haematologica. 2007;92:854-5.
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  56. VOSKARIDOU E , Tsetsos G, Tsoutsias A, Spyropoulou E, et al
    Pulmonary hypertension in patients with sickle cell/beta thalassemia: incidence and correlation with serum N-terminal pro-brain natriuretic peptide concentrations.
    Haematologica. 2007;92:738-43.
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  57. ZANELLA A , Bianchi P, Fermo E
    Pyruvate kinase deficiency.
    Haematologica. 2007;92:721-3.
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    May 2007
  58. MAURY S , Balere-Appert ML, Chir Z, Boiron JM, et al
    Unrelated stem cell transplantation for severe acquired aplastic anemia: improved outcome in the era of high-resolution HLA matching between donor and recipient.
    Haematologica. 2007;92:589-96.
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  59. POSPISILOVA D , Cmejlova J, Hak J, Adam T, et al
    Successful treatment of a Diamond-Blackfan anemia patient with amino acid leucine.
    Haematologica. 2007;92:92e066.
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  60. WINICHAGOON P , Svasti S, Winichagoon P, Chitchumroonchokchai C, et al
    Expression of betaE and gamma-globin genes in infants heterozygous for hemoglobin E and double heterozygous for hemoglobin E and alpha-thalassemia.
    Haematologica. 2007;92:702-3.
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  61. AESSOPOS A , Kati M, Farmakis D
    Heart disease in thalassemia intermedia: a review of the underlying pathophysiology.
    Haematologica. 2007;92:658-65.
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  62. LEE KH , Park SS, Kim I, Kim JH, et al
    P2X7 receptor polymorphism and clinical outcomes in HLA-matched sibling allogeneic hematopoietic stem cell transplantation.
    Haematologica. 2007;92:651-7.
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  63. ORIGA R , Galanello R, Ganz T, Giagu N, et al
    Liver iron concentrations and urinary hepcidin in beta-thalassemia.
    Haematologica. 2007;92:583-8.
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  64. WAYE JS , Chui DH
    Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
    Haematologica. 2007;92:e68.
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    April 2007
  65. DMOSZYNSKA A , Kloczko J, Rokicka M, Hellmann A, et al
    A dose exploration, phase I/II study of administration of continuous erythropoietin receptor activator once every 3 weeks in anemic patients with multiple myeloma receiving chemotherapy.
    Haematologica. 2007;92:493-501.
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  66. WOLF T , Rickerts V, Staszewski S, Kriener S, et al
    First case of successful allogeneic stem cell trans- plantation in an HIV-patient who acquired severe Aplastic Anemia.
    Haematologica. 2007;92:92e056.
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    March 2007
  67. GIRODON F , Lippert E, Mossuz P, Dobo I, et al
    JAK2V617F detection and dosage of serum erythropoietin: first steps of the diagnostic work-up for patients consulting for elevated hematocrit.
    Haematologica. 2007;92:431-2.
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  68. ZDEBSKA E , Iolascon A, Spychalska J, Perrotta S, et al
    Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease gene.
    Haematologica. 2007;92:427-8.
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  69. COUILLARD S , Benkerrou M, Girot R, Brousse V, et al
    Steroid treatment in children with sickle-cell disease.
    Haematologica. 2007;92:425-6.
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  70. FRISCHKNECHT H , Dutly F
    A 65 bp duplication/insertion in exon II of the beta globin gene causing beta0-thalassemia.
    Haematologica. 2007;92:423-4.
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  71. HILL A , Richards SJ, Rother RP, Hillmen P, et al
    Erythopoietin treatment during complement inhibition with eculizumab in a patient with paroxysmal nocturnal hemoglobinuria.
    Haematologica. 2007;92:e31-3.
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  72. MALIK M , Pillai LS, Gogia N, Puri T, et al
    Paraplegia due to extramedullary hematopoiesis in thalassemia treated successfully with radiation therapy.
    Haematologica. 2007;92:e28-30.
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    February 2007
  73. BAZRGAR M , Karimi M, Peiravian F, Fathzadeh M, et al
    Apolipoprotein E gene polymorphism and left ventricular function in Iranian patients with thalassemia major.
    Haematologica. 2007;92:256-7.
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  74. LACERRA G , Musollino G, Di Noce F, Prezioso R, et al
    Genotyping for known Mediterranean alpha-thalassemia point mutations using a multiplex amplification refractory mutation system.
    Haematologica. 2007;92:254-5.
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  75. GOMES S , Picanco I, Miranda A, Seixas MT, et al
    Hb Evora [alpha2-35 (B16), Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.
    Haematologica. 2007;92:252-3.
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  76. DE FOST M , Aerts JM, Groener JE, Maas M, et al
    Low frequency maintenance therapy with imiglucerase in adult type I Gaucher disease: a prospective randomized controlled trial.
    Haematologica. 2007;92:215-21.
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  77. FONTE R , Agosti A, Scafa F, Candura SM, et al
    Anaemia and abdominal pain due to occupational lead poisoning.
    Haematologica. 2007;92:e13-4.
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    January 2007
  78. LOCASCIULLI A , Oneto R, Bacigalupo A, Socie G, et al
    Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunosuppressive treatment in the last decade: a report from the European Group for Blood and Marrow Transplantation (EBMT).
    Haematologica. 2007;92:11-8.
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  79. MARSH JC
    Treatment of acquired aplastic anemia.
    Haematologica. 2007;92:2-5.
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  80. AESSOPOS A , Fragodimitri C, Karabatsos F, Hatziliami A, et al
    Cardiac magnetic resonance imaging R2* assessments and analysis of historical parameters in patients with transfusion-dependent thalassemia.
    Haematologica. 2007;92:131-2.
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  81. COLOSIMO A , Guida V, Antonucci I, Bonfini T, et al
    Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cells.
    Haematologica. 2007;92:129-30.
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  82. BARCELLINI W , Zaninoni A, Imperiali FG, Boschetti C, et al
    Anti-erythroblast autoimmunity in early myelodysplastic syndromes.
    Haematologica. 2007;92:19-26.
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    December 2006
  83. STEENSMA DP , Caudill JS, Pardanani A, McClure RF, et al
    MPL W515 and JAK2 V617 mutation analysis in patients with refractory anemia with ringed sideroblasts and an elevated platelet count.
    Haematologica. 2006;91.
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  84. BARCELLINI W , Capalbo S, Agostinelli RM, Mauro FR, et al
    Relationship between autoimmune phenomena and disease stage and therapy in B-cell chronic lymphocytic leukemia.
    Haematologica. 2006;91:1689-92.
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  85. DE MONTALEMBERT M , Bachir D, Hulin A, Gimeno L, et al
    Pharmacokinetics of hydroxyurea 1,000 mg coated breakable tablets and 500 mg capsules in pediatric and adult patients with sickle cell disease.
    Haematologica. 2006;91:1685-8.
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  86. GIAMBONA A , Passarello C, Ruggeri G, Renda D, et al
    Analysis of delta-globin gene alleles in the Sicilian population: identification of five new mutations.
    Haematologica. 2006;91:1681-4.
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  87. HARTMANN JT , Meisinger I, Krober SM, Weisel K, et al
    Progressive bicytopenia due to persistent parvovirus B19 infection after immunochemotherapy with fludarabine/cyclophosphamide and rituximab for relapsed B cell lymphoma.
    Haematologica. 2006;91.
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    November 2006
  88. CMEJLOVA J , Dolezalova L, Pospisilova D, Petrtylova K, et al
    Translational efficiency in patients with Diamond-Blackfan anemia.
    Haematologica. 2006;91:1456-64.
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  89. VON LINDERN M
    Reduced protein synthesis in Diamond-Blackfan anemia.
    Haematologica. 2006;91:1441A.
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  90. BENTO C , Relvas L, Vazao H, Campos J, et al
    The use of capillary blood samples in a large scale screening approach for the detection of beta-thalassemia and hemoglobin variants.
    Haematologica. 2006;91:1565.
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  91. IRENGE LM , Robert A, Gala JL
    Quantitative assessment of the transcriptional impact of mutations in the 3'untranslated region of the human beta-globin gene: application to the +1480 C-->G mutation.
    Haematologica. 2006;91:1563-4.
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    October 2006
  92. TANNER MA , He T, Westwood MA, Firmin DN, et al
    Multi-center validation of the transferability of the magnetic resonance T2* technique for the quantification of tissue iron.
    Haematologica. 2006;91:1388-91.
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  93. GALANELLO R , Piga A, Forni GL, Bertrand Y, et al
    Phase II clinical evaluation of deferasirox, a once-daily oral chelating agent, in pediatric patients with beta-thalassemia major.
    Haematologica. 2006;91:1343-51.
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  94. DE FRANCESCHI L , Daraio F, Filippini A, Carturan S, et al
    Liver expression of hepcidin and other iron genes in two mouse models of beta-thalassemia.
    Haematologica. 2006;91:1336-42.
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  95. RAMAN SV , Simonetti OP, Cataland SR, Kraut EH, et al
    Myocardial ischemia and right ventricular dysfunction in adult patients with sickle cell disease.
    Haematologica. 2006;91:1329-35.
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  96. YAN T , Cai R, Mo O, Zhu D, et al
    Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.
    Haematologica. 2006;91:1321-8.
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  97. LUZZATTO L
    Glucose 6-phosphate dehydrogenase deficiency: from genotype to phenotype.
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  98. JAMET D , Pissard S, Blouch MT, Berthou C, et al
    Beta-thalassemia in the indigenous population of Brittany: identification of three rare mutations.
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  99. CECI A , Baiardi P, Catapano M, Felisi M, et al
    Risk factors for death in patients with beta-thalassemia major: results of a case-control study.
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    September 2006
  100. CHAAR V , Tarer V, Etienne-Julan M, Diara JP, et al
    ET-1 and ecNOS gene polymorphisms andsusceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia.
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  101. CHIARELLI LR , Fermo E, Abrusci P, Bianchi P, et al
    Two new mutations of the P5ON-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.
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  102. PANIGRAHI I , Agarwal S, Pradhan M, Choudhry DR, et al
    Molecular characterization of thalassemia intermedia in Indians.
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  103. GUIDA V , Cappabianca MP, Colosimo A, Rafanelli F, et al
    Influence of Ggamma-158C --> and beta- (AT)x(T)y globin gene polymorphisms on HbF levels in Italian beta-thalassemia carriers and wild-type subjects.
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  104. GALANELLO R , Kattamis A, Piga A, Fischer R, et al
    A prospective randomized controlled trial on the safety and efficacy of alternating deferoxamine and deferiprone in the treatment of iron overload in patients with thalassemia.
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  105. VOSKARIDOU E , Anagnostopoulos A, Konstantopoulos K, Stoupa E, et al
    Zoledronic acid for the treatment of osteoporosis in patients with beta-thalassemia: results from a single-center, randomized, placebo-controlled trial.
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  106. TELFER P , Coen PG, Christou S, Hadjigavriel M, et al
    Survival of medically treated thalassemia patients in Cyprus. Trends and risk factors over the period 1980-2004.
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  107. BORGNA-PIGNATTI C
    Thalassemia. A few new tiles in a large mosaic.
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  108. MAHACHOKLERTWATTANA P
    Zoledronic acid for the treatment of thalassemia-induced osteonecrosis.
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  109. PIGA A
    Survival improvement in thalassemia: who should take the credit?
    Haematologica. 2006;91:1154B.
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    August 2006
  110. CHAAR V , Tarer V, Etienne-Julan M, Diara JP, et al
    ET-1 and ecNOS gene polymorphisms and susceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia.
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  111. CHIARELLI LR , Fermo E, Abrusci P, Bianchi P, et al
    Two new mutations of P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.
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  112. LITTLE JA , McGowan VR, Kato GJ, Partovi KS, et al
    Combination erythropoietin-hydroxyurea therapy in sickle cell disease: experience from the National Institutes of Health and a literature review.
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  113. NUAMAH NM , Hamaloglu E, Ozdemir A, Ozenc A, et al
    Hepatic focal nodular hyperplasia developing in a Fanconi anemia patient: a case report and literature review.
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  114. MANTADAKIS E , Boula AM, Girakis G, Xilouri IM, et al
    Transient loss of the Y-chromosome in an elderly man with anemia and lead poisoning: Chance occurrence or a clonal marker of the underlying hematological abnormality?
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    July 2006
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    The effects of microdose recombinant human erythropoietin regimens in athletes.
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  116. PIGA A , Galanello R, Forni GL, Cappellini MD, et al
    Randomized phase II trial of deferasirox (Exjade, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload.
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    June 2006
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    Megaloblastic anemia in North Africa.
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  118. JABR FI , Taher A
    Diamond-Blackfan anemia in remission for 2 years on valproic acid.
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  119. CAULI C , Serra G, Chessa L, Balestrieri C, et al
    Severe autoimmune hemolytic anemia in a patient with chronic hepatitis C during treatment with peginterferon alfa-2a and ribavirin.
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  120. KONTOGHIORGHES GJ , Kolnagou A
    Effective new treatments of iron overload in thalassaemia using the ICOC combination therapy protocol of deferiprone (L1) and deferoxamine and of new chelating drugs.
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  121. TAVECCHIA L , Masera N, Russo P, Ciro A, et al
    Successful recovery of acute hemosiderotic heart failure in beta-thalassemia major treated with a combined regimen of desferrioxamine and deferiprone.
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  122. SHEIKH-TAHA M , Koussa S, Taher A
    Isolated thrombocytopenia associated with hydroxyurea/deferiprone (L1) therapy in a sickle beta thalassemia patient.
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  123. FARTOUKH M , Prigent H, Thioliere B, Enache-Angoulvant A, et al
    Fatal fungal superinfection complicating B19 virus-induced massive bone marrow necrosis in sickle-cell disease.
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    First report on the co-inheritance of (beta) IVS I-1 (G-->T) Thalassemia with the (gamma) CD85 [Phe-->Ser (F1) (TTT-->TCT)] HbA2 Etolia in Iran.
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    The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.
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  126. NEMETH E , Ganz T
    Hepcidin and iron-loading anemias.
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  127. GLADWIN MT
    Polycythemia, HIF-1alpha and pulmonary hypertension in Chuvash.
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    The frequency of HLA class I alleles in Japanese patients with bone marrow failure.
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    Osteoporosis and osteosclerosis in sickle cell/beta-thalassemia: the role of the RANKL/osteoprotegerin axis.
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    May 2006
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    Occurrence of the JAK2 V617F mutation in the WHO provisional entity: myelodysplastic/myeloproliferative disease, unclassifiable-refractory anemia with ringed sideroblasts associated with marked thrombocytosis.
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    Predicting erythroid response to recombinant erythropoietin plus granulocyte colony-stimulating factor therapy following a single subcutaneous bolus in patients with myelodysplasia.
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  132. CHEUNG WW , Hwang GY, Tse E, Kwong YL, et al
    Alemtuzumab induced complete remission of autoimmune hemolytic anemia refractory to corticosteroids, splenectomy and rituximab.
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  133. WONDERGEM MJ , Overbeeke M, Som N, Chamuleau ME, et al
    Mixed autoimmune haemolysis in a SLE patient due to aspecific and anti-Jka autoantibodies; case report and review of the literature.
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    Exchange blood transfusions for the treatment of leg ulcerations in thalassemia intermedia.
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    Antithymocyte globulin and cyclosporine A as combination therapy for low-risk non-sideroblastic myelodysplastic syndromes.
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  137. SABINA RL , Waldenstrom A, Ronquist G
    The contribution of Ca+ calmodulin activation of human erythrocyte AMP deaminase (isoform E) to the erythrocyte metabolic dysregulation of familial phosphofructokinase deficiency.
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  138. LI D , Liao C, Li J, Xie X, et al
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    April 2006
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    Mutations in telomerase catalytic protein in Japanese children with aplastic anemia.
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  140. BERENTSEN S , Ulvestad E, Langholm R, Beiske K, et al
    Primary chronic cold agglutinin disease: a population based clinical study of 86 patients.
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    Cold agglutinin disease.
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  142. GAMBERALE R , Fernandez-Calotti P, Sanchez-Avalos J, Alberto MF, et al
    The effect of fludarabine on interferon-gamma production by lymphoid cells from healthy donors and patients with B-cell chronic lymphocytic leukemia.
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  143. HARTEVELD CL , Steen G, Vlasveld LT, van Delft P, et al
    Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
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    March 2006
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    Spectrum of beta-thalassemia mutations in various regions of Punjab and Islamabad, Pakistan: establishment of prenatal diagnosis.
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  145. DELLUC A , Pasquier E, de Saint Martin L, Mottier D, et al
    Rituximab's cost for the treatment of primary cold agglutinin disease should not limit its use.
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  146. WORWOOD M
    Iron regulatory protein 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency.
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  147. GUIDA V , Colosimo A, Fichera M, Lombardo T, et al
    Hematologic and molecular characterization of a Sicilian cohort of alpha thalassemia carriers.
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    Iron regulatory proteins 1 and 2 in human monocytes, macrophages and duodenum: expression and regulation in hereditary hemochromatosis and iron deficiency.
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    February 2006
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    The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal.
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    January 2006
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    Known and new delta globin gene mutations and their diagnostic significance.
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  151. DE MONTALEMBERT M , Brousse V, Elie C, Bernaudin F, et al
    Long-term hydroxyurea treatment in children with sickle cell disease: tolerance and clinical outcomes.
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  152. ALIYU ZY , Tumblin AR, Kato GJ
    Current therapy of sickle cell disease.
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    December 2005
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    Abnormal positron emission tomography (PET) scan secondary to the use of hematopoietic growth factors.
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  154. CAMPBELL CD , Ganesh J, Ficicioglu C
    Two newborns with nutritional vitamin B12 deficiency: challenges in newborn screening for vitamin B12 deficiency.
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  155. HILL A , Rother RP, Hillmen P
    Improvement in the symptoms of smooth muscle dystonia during eculizumab therapy in paroxysmal nocturnal hemoglobinuria.
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    November 2005
  156. GIORDANO PC
    Brief comment on the case report by Fattori et al. 2005 (5) 589-590.
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  157. GULEN H , Basarir F, Hakan N, Ciftdogan DY, et al
    Premature labor and leukoerythroblastosis in a newborn with parvovirus B19 infection.
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  158. HELBIG G , Stella-Holowiecka B, Krawczyk-Kulis M, Wojnar J, et al
    Successful treatment of pure red cell aplasia with repeated, low doses of rituximab in two patients after ABO-incompatible allogeneic haematopoietic stem cell transplantation for acute myeloid leukaemia.
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    Paravertebral extramedullary hematopoiesis due to pyruvate kinase deficiency.
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    Membranous glomerulopathy in children given allogeneic hematopoietic stem cell transplantation.
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    Cerebellar degeneration and folate deficiency due to cough mixture abuse.
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  162. QUACH H , Januszewicz H, Westerman D
    Complete remission of hairy cell leukemia variant (HCL-v) complicated by red cell aplasia post treatment with rituximab.
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  163. FRISCHKNECHT H , Kiewitz R, Schmugge M
    A 4 base pair TGAT insertion at codon 116 of the beta globin gene causes beta0-thalassemia.
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    April 2005
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    Nutritional iron status in children with alpha+ thalassemia and the sickle cell trait in a malaria endemic area on the coast of Kenya.
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  165. GIORDANO PC , Bouva MJ, Van Delft P, Akkerman N, et al
    A new polyadenylation site mutation associated with a mild beta-thalassemia phenotype.
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    Mature erythrocyte indices: new markers of iron availability.
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    March 2005
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    Decreased plasma endothelin-1 levels in children with sickle cell disease treated with hydroxyurea.
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    January 2005
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    Sustained response to interferon a-2a in thalassemic patients with chronic hepatitis C. A prospective 8-year follow-up study.
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