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Am J Hematol
- CHEE CE
, Steensma DP, Wu W, Hanson CA, et al
Neither serum ferritin nor the number of red blood cell transfusions affect overall survival in refractory anemia with ringed sideroblasts.
Am J Hematol. 2008;.
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- SHARMA R
, Prakash R, Kamboj S, Jain V, et al
Hemoglobin-E beta thalassemia presenting with recurrent priapism--a rare complication.
Am J Hematol. 2008;83:257.
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- GARIBALDI B
, King KE, Jaffe JM, Moliterno AR, et al
Hypersplenism induced by splenic vein ligation.
Am J Hematol. 2008;83:242-4.
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- DARBARI DS
, van Schaik RH, Capparelli EV, Rana S, et al
UGT2B7 promoter variant -840G>A contributes to the variability in hepatic clearance of morphine in patients with sickle cell disease.
Am J Hematol. 2008;83:200-2.
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- SHORD SS
, Chew L, Villano J
Evaluation of opioid induced nausea and vomiting in sickle cell disease.
Am J Hematol. 2008;83:196-9.
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- DARBARI DS
, Minniti CP, Rana S, van den Anker J, et al
Pharmacogenetics of morphine: Potential implications in sickle cell disease.
Am J Hematol. 2008;83:233-6.
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Ann Hematol
- ROPERO P
, Gonzalez FA, Villas JM, Paul R, et al
The novo 4 BP deletion in the codons 20/21 (-TGGA) at the first exon of the beta-globin gene causing a beta0-thalassemia in a Spanish male.
Ann Hematol. 2008;87:63-5.
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- BEYAN C
, Kaptan K, Ifran A
Discrimination indices as screening tests for beta-thalassemia trait.
Ann Hematol. 2008;87:61-2.
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Arch Pediatr
- CARDORELLE AM
, Mouko A
[Acute anaemia in the child Congolese drepanocytaire]
Arch Pediatr. 2008;15:198-9.
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Br J Haematol
- KURAMITSU M
, Hamaguchi I, Takuo M, Masumi A, et al
Deficient RPS19 protein production induces cell cycle arrest in erythroid progenitor cells.
Br J Haematol. 2008;140:348-59.
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- KELAIDI C
, Eclache V, Fenaux P
The role of lenalidomide in the management of myelodysplasia with del 5q.
Br J Haematol. 2008;140:267-78.
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- QUINN CT
, Sargent JW
Daytime steady-state haemoglobin desaturation is a risk factor for overt stroke in children with sickle cell anaemia.
Br J Haematol. 2008;140:336-9.
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J Clin Invest
- WEBER YG
, Storch A, Wuttke TV, Brockmann K, et al
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
J Clin Invest. 2008;.
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J Trop Pediatr
- KAYA AD
, Gencay E, Ozturk CE, Yavuz T, et al
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- CANAVESE C
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Think of Oxalate when Using Ascorbate Supplementation to Optimize Iron theRapy in Dialysis Patients.
Nephrol Dial Transplant. 2007;.
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- PASHANKAR FD
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