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Andre E, Chevalier C, Scheiff JM. Howell-Jolly-like bodies in leucocytes: first description in leucocytes other than neutrophils. Eur J Haematol. 2011 Feb;86(2):182-3. doi: 10.1111/j.1600-0609.2010.01543.x. Epub 2010 Dec 29. PubMed PMID: 20964720. Gifford AH, Miller SD, Jackson BP, Hampton TH, O'Toole GA, Stanton BA, Parker HW. Iron and CF-related anemia: expanding clinical and biochemical relationships. Pediatr Pulmonol. 2011 Feb;46(2):160-5. doi: 10.1002/ppul.21335. Epub 2010 Oct 20. PubMed PMID: 20963784. Kautz L, Besson-Fournier C, Meynard D, Latour C, Roth MP, Coppin H. Iron overload induces BMP6 expression in the liver but not in the duodenum. Haematologica. 2011 Feb;96(2):199-203. Epub 2010 Oct 15. PubMed PMID: 20952515; PubMed Central PMCID: PMC3031686. Noetzli LJ, Carson S, Coates TD, Wood JC. Revisiting the relationship between vitamin D deficiency, cardiac iron and cardiac function in thalassemia major. Eur J Haematol. 2011 Feb;86(2):176-7. doi: 10.1111/j.1600- 0609.2010.01538.x. Epub 2010 Dec 22. PubMed PMID: 20942841. Lee FS, Percy MJ. The HIF pathway and erythrocytosis. Annu Rev Pathol. 2011 Feb 28;6:165-92. PubMed PMID: 20939709. Ganz T, Nemeth E. Hepcidin and disorders of iron metabolism. Annu Rev Med. 2011 Feb 18;62:347-60. PubMed PMID: 20887198. Beksac MS, Gumruk F, Gurgey A, Cakar N, Mumusoglu S, Ozyuncu O, Altay C. Prenatal diagnosis of hemoglobinopathies in Hacettepe University, Turkey. Pediatr Hematol Oncol. 2011 Feb;28(1):51-5. Epub 2010 Sep 23. PubMed PMID: 20863160. Kitajima J, Ohga S, Kinjo T, Ochiai M, Takahata Y, Honjo S, Hara T. Serum prohepcidin concentrations at birth and 1 month after birth in premature infants. Pediatr Blood Cancer. 2011 Feb;56(2):267-72. doi: 10.1002/pbc.22773. Epub 2010 Sep 9. PubMed PMID: 20830780. Green NS, Barral S. Genetic modifiers of HbF and response to hydroxyurea in sickle cell disease. Pediatr Blood Cancer. 2011 Feb;56(2):177-81. doi: 10.1002/pbc.22754. Epub 2010 Sep 9. Review. PubMed PMID: 20830771; PubMed Central PMCID: PMC3006002. Cassart M, Avni FE, Guibaud L, Molho M, D'Haene N, Paupe A. Fetal liver iron overload: the role of MR imaging. Eur Radiol. 2011 Feb;21(2):295-300. Epub 2010 Sep 4. PubMed PMID: 20821014.
Fargion S, Valenti L, Fracanzani AL. Beyond hereditary hemochromatosis: new insights into the relationship between iron overload and chronic liver diseases. Dig Liver Dis. 2011 Feb;43(2):89-95. Epub 2010 Aug 24. PubMed PMID: 20739232. Adams PC, Beaton MD. Transferrin saturation as a predictor of hepatic iron overload. Liver Int. 2011 Feb;31(2):272-3. doi: 10.1111/j.1478- 3231.2010.02335.x. Epub 2010 Aug 25. PubMed PMID: 20738776. Marcí M, Pitrolo L, Lo Pinto C, Sanfilippo N, Malizia R. Detection of early cardiac dysfunction in patients with Beta thalassemia by tissue Doppler echocardiography. Echocardiography. 2011 Feb;28(2):175-80. doi: 10.1111/j.1540-8175.2010.01270.x. Epub 2010 Aug 24. PubMed PMID: 20738369. Chen LY, Chang SD, Sreenivasan GM, Tsang PW, Broady RC, Li CH, Zypchen LN. Dysmetabolic hyperferritinemia is associated with normal transferrin saturation, mild hepatic iron overload, and elevated hepcidin. Ann Hematol. 2011 Feb;90(2):139-43. Epub 2010 Aug 19. PubMed PMID: 20721554. Tripathi A, Jerrell JM, Stallworth JR. Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease. Ann Hematol. 2011 Feb;90(2):145-50. Epub 2010 Aug 17. PubMed PMID: 20714723. Phylipsen M, Gallivan MV, Arkesteijn SG, Harteveld CL, Giordano PC. Occurrence of common and rare δ-globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ-globin gene defects in β-thalassemia diagnostics. Int J Lab Hematol. 2011 Feb;33(1):85- 91. doi: 10.1111/j.1751-553X.2010.01255.x. PubMed PMID: 20678137. Vichinsky EP, Ohene-Frempong K; Transfusion Committee. Approaches to transfusion therapy and iron overload in patients with sickle cell disease: results of an international survey. Pediatr Hematol Oncol. 2011 Feb;28(1):37- 42. Epub 2010 Jul 30. PubMed PMID: 20673029. Shang X, Rao Z, Lou J, Li W, Xiong F, Zhou HP, Xu X. Compound heterozygosity for a rare small deletion and a common point mutation in the beta-globin gene: report of two Chinese families. Int J Lab Hematol. 2011 Feb;33(1):79-84. doi: 10.1111/j.1751-553X.2010.01253.x. PubMed PMID: 20649908. Gupte RS, Ata H, Rawat D, Abe M, Taylor MS, Ochi R, Gupte SA. Glucose-6phosphate dehydrogenase is a regulator of vascular smooth muscle contraction. Antioxid Redox Signal. 2011 Feb 15;14(4):543-58. Epub 2010 Oct 25. PubMed PMID: 20649491; PubMed Central PMCID: PMC3029003.
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