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Cardiac T2* MRI assessment in patients with thalassaemia major and its effect on the preference of chelation therapyAKCAY, Arzu; SALCIOGLU, Zafer; OZTARHAN, Kazim et al.International journal of hematology. 2014, Vol 99, Num 6, pp 706-713, issn 0925-5710, 8 p.Article

Clinical signs and symptoms associated with increased risk for thrombosis in patients with paroxysmal nocturnal hemoglobinuria from a Korean RegistryJONG WOOK LEE; JUN HO JANG; JIN SEOK KIM et al.International journal of hematology. 2013, Vol 97, Num 6, pp 749-757, issn 0925-5710, 9 p.Article

First reported case of compound heterozygosity for HbA2-Yialousa (HBD: c.82 G>C) and HbA2-Wrens (HBD: c.295 G>A) in OmanSHOAIB AL ZADJALI; BASHIR, Wafa; GRAVELL, David et al.International journal of hematology. 2013, Vol 98, Num 2, pp 240-242, issn 0925-5710, 3 p.Article

Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acidsVASAVDA, Nisha; WOODLEY, Claire; ALLMAN, Marlene et al.British journal of haematology. 2012, Vol 157, Num 2, pp 249-252, issn 0007-1048, 4 p.Article

Keeping it in the family: Three relatives with HbSC disease and simultaneous acute pulmonary emboliHAWKINS, Finn; EBEL, Noelle; SORESCU, George P et al.American journal of hematology. 2012, Vol 87, Num 1, pp 101-104, issn 0361-8609, 4 p.Article

The cause of sudden anemia revealed by the blood filmBHARADWAJ, Vandana; CHAKRAVORTY, Subarna; BAIN, Barbara J et al.American journal of hematology. 2012, Vol 87, Num 5, issn 0361-8609, p. 520Article

Using the hemoglobin switch for the treatment of sickle cell diseaseCOOLS, Jan.Haematologica (Roma). 2012, Vol 97, Num 2, issn 0390-6078, p. 156Article

An unexpectedly bizarre blood film in hemoglobin H diseaseCHAKRAVORTY, S; KING, M. J; BAIN, B. J et al.American journal of hematology. 2012, Vol 87, Num 12, issn 0361-8609, p. 1104Article

A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA1cNISHIMORI, Hisakazu; HARANO, Keiko; WADA, Hideho et al.International journal of hematology. 2012, Vol 95, Num 6, pp 697-701, issn 0925-5710, 5 p.Article

Diagnosis and treatment of cold agglutinin mediated autoimmune hemolytic anemiaBERENTSEN, Sigbjørn; TJØNNFJORD, Geir E.Blood reviews. 2012, Vol 26, Num 3, pp 107-115, issn 0268-960X, 9 p.Article

Elevated plasma levels and platelet-associated expression of the pro-thrombotic and pro-inflammatory protein, TNFSF14 (LIGHT), in sickle cell diseaseGARRIDO, Vanessa T; PROENCA-FERREIRA, Renata; CONRAN, Nicola et al.British journal of haematology. 2012, Vol 158, Num 6, pp 788-797, issn 0007-1048, 10 p.Article

Heme metabolism and erythropoiesisCHUNG, Jacky; CAIYONG CHEN; PAW, Barry H et al.Current opinion in hematology. 2012, Vol 19, Num 3, pp 156-162, issn 1065-6251, 7 p.Article

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI geneWARANG, Prashant; KEDAR, Prabhakar; GHOSH, Kanjaksha et al.International journal of hematology. 2012, Vol 96, Num 2, pp 263-267, issn 0925-5710, 5 p.Article

Prevalence of transcranial Doppler abnormalities in Nigerian children with sickle cell diseaseLAGUNJU, Ikeoluwa; SODEINDE, Olugbemiro; TELFER, Paul et al.American journal of hematology. 2012, Vol 87, Num 5, pp 544-547, issn 0361-8609, 4 p.Article

Red blood cell alloimmunization in sickle cell disease: pathophysiology, risk factors, and transfusion managementYAZDANBAKHSH, Karina; WARE, Russell E; NOIZAT-PIRENNE, France et al.Blood. 2012, Vol 120, Num 3, pp 528-537, issn 0006-4971, 10 p.Article

Renal iron load in sickle cell disease is influenced by severity of haemolysisVASAVDA, Nisha; GUTIERREZ, Lucia; HOUSE, Michael J et al.British journal of haematology. 2012, Vol 157, Num 5, pp 599-605, issn 0007-1048, 7 p.Article

Thrombin generation reveals high procoagulant potential in the plasma of sickle cell disease childrenNOUBOUOSSIE, Denis F; QUOC LE, Phu; CORAZZA, Francis et al.American journal of hematology. 2012, Vol 87, Num 2, pp 145-149, issn 0361-8609, 5 p.Article

High frequency of ribosomal protein gene deletions in Italian Diamond-Blackfan anemia patients detected by multiplex ligation-dependent probe amplification assayQUARELLO, Paola; GARELLI, Emanuela; BRUSCO, Alfredo et al.Haematologica (Roma). 2012, Vol 97, Num 12, pp 1813-1817, issn 0390-6078, 5 p.Article

Molecular mechanisms of pathology and treatment in Diamond Blackfan AnaemiaHOROS, Rastislav; VON LINDERN, Marieke.British journal of haematology. 2012, Vol 159, Num 5, pp 514-527, issn 0007-1048, 14 p.Article

Advances in the treatment of alpha-thalassemiaVICHINSKY, Elliott.Blood reviews. 2012, Vol 26, issn 0268-960X, S31-S34, SUP1Article

Anémie, EPO et anti-émétiques = Anemia, erythropoïesis stimulating agents and anti-emesisDESCOURT, R; CHENEAU, C; DECROISETTE, C et al.Revue des maladies respiratoires actualités (Print). 2012, Vol 4, Num 6, pp 537-542, issn 1877-1203, 6 p.Conference Paper

Darbepoetin alfa for the treatment of anaemia in alpha- or beta-thalassaemia intermedia syndromesSINGER, Sylvia T; VICHINSKY, Elliott P; SWEETERS, Nancy et al.British journal of haematology. 2011, Vol 154, Num 2, pp 281-284, issn 0007-1048, 4 p.Article

Direct antiglobulin test-negative autoimmune hemolytic anemia associated with HLA-haploidentical stem cell transplantationNAKATA, Jun; TAMAKI, Hiroya; IKEGAME, Kazuhiro et al.International journal of hematology. 2011, Vol 93, Num 4, pp 558-560, issn 0925-5710, 3 p.Article

Reversibility of spur cell anemiaGERBER, Bernhard; STUSSI, Georg.Blood. 2011, Vol 118, Num 16, issn 0006-4971, p. 4304Article

Vitamin D deficiency and chronic pain in sickle cell diseaseZIEGLER, Thomas R; OFORI-ACQUAH, Solomon; TANGPRICHA, Vin et al.ZIEGLER, Thomas R; OFORI-ACQUAH, Solomon; TANGPRICHA, Vin et al.British journal of haematology. 2011, Vol 153, Num 4, pp 538-540, issn 0007-1048, 3 p.Article

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