Search Results

No evidence for myocardial iron overload and free iron species in multitransfused patients with sickle/β⁰-thalassaemia

Authors: Ghoti, Hussam; Goitein, Orly; Koren, Ariel; Levin, Carina; Kushnir, Tamar; Rachmilewitz, Eliezer; Konen, Eli

Source: European Journal of Haematology, Volume 84, Number 1, January 2010 , pp. 59-63(5)

Publisher: Blackwell Publishing

Elevated serum parathormone levels are associated with myocardial iron overload in patients with β-thalassaemia major

Authors: Dimitriadou, Meropi; Christoforidis, Athanasios; Economou, Marina; Tsatra, Ioanna; Vlachaki, Efthimia; Fidani, Liana; Katzos, George; Athanassiou-Metaxa, Miranda

Source: European Journal of Haematology, Volume 84, Number 1, January 2010 , pp. 64-71(8)

Publisher: Blackwell Publishing

Multiplex ligation-dependent probe amplification screening of isolated increased HbF levels revealed three cases of novel rearrangements/deletions in the β-globin gene cluster

Authors: Lee, Seung-Tae; Yoo, Eun-Hyung; Kim, Ji-Youn; Kim, Jong-Won; Ki, Chang-Seok

Source: British Journal of Haematology, Volume 148, Number 1, January 2010 , pp. 154-160(7)

Publisher: Blackwell Publishing

Treatment with deferasirox (Exjade^®) effectively decreases iron burden in patients with thalassaemia intermedia: results of a pilot study

Authors: Voskaridou, Ersi; Plata, Eleni; Douskou, Maroussa; Papadakis, Manousos; Delaki, Eleni-Evangelia; Christoulas, Dimitrios; Terpos, Evangelos

Source: British Journal of Haematology, Volume 148, Number 2, January 2010 , pp. 332-334(3)

Publisher: Blackwell Publishing

Skin, muscle and joint disease from the 17th century: scurvy

Authors: LAU, Herman; MASSASSO, David; JOSHUA, Fredrick

Source: International Journal of Rheumatic Diseases, Volume 12, Number 4, December 2009 , pp. 361-365(5)

Publisher: Blackwell Publishing

Iron overload in thalassaemia intermedia: reassessment of iron chelation strategies

Authors: Taher, Ali; Hershko, Chaim; Cappellini, Maria Domenica

Source: British Journal of Haematology, Volume 147, Number 5, December 2009 , pp. 634-640(7)

Publisher: Blackwell Publishing

Daily labile plasma iron as an indicator of chelator activity in Thalassaemia major patients

Authors: Zanninelli, Giuliana; Breuer, William; Cabantchik, Zvi I.

Source: British Journal of Haematology, Volume 147, Number 5, December 2009 , pp. 744-751(8)

Publisher: Blackwell Publishing

Efficacy and safety of deferasirox doses of >30 mg/kg per d in patients with transfusion-dependent anaemia and iron overload

Authors: Taher, Ali; Cappellini, Maria D.; Vichinsky, Elliott; Galanello, Renzo; Piga, Antonio; Lawniczek, Tomasz; Clark, Joan; Habr, Dany; Porter, John B.

Source: British Journal of Haematology, Volume 147, Number 5, December 2009 , pp. 752-759(8)

Publisher: Blackwell Publishing

The changing face of homozygous sickle cell disease: 102 patients over 60 years

Authors: SERJEANT, G. R.; SERJEANT, B. E.; MASON, K. P.; HAMBLETON, I. R.; FISHER, C.; HIGGS, D. R.

Source: International Journal of Laboratory Hematology, Volume 31, Number 6, December 2009 , pp. 585-596(12)

Publisher: Blackwell Publishing

Molecular variants and clinical importance of β-thalassaemia traits found in the state of Orissa, India

Authors: Nishank, Sudhansu Sekhar; Ranjit, Manoranjan; Kar, Shantanu K.; Chhotray, Guru Prasad

Source: Hematology, Volume 14, Number 5, October 2009 , pp. 290-296(7)

Publisher: Maney Publishing

The use of real-time PCR technique in the detection of novel protein 4.2 gene mutations that coexist with thalassaemia alpha in a single patient

Authors: Maciag, Monika; Adamowicz-Salach, Anna; Siwicka, Alicja; Spychalska, Justyna; Burzynska, Beata

Source: European Journal of Haematology, Volume 83, Number 4, October 2009 , pp. 373-377(5)

Publisher: Blackwell Publishing

Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [β122 (GH5) Phe→Ser], a probable case of germ line mutation, and Hb Olinda [β22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequence

Authors: Bezerra, Marcos A. C.; Albuquerque, Dulcinéia M.; Santos, Magnun N. N.; Kimura, Elza M.; Jorge, Susan E. D. C.; Oliveira, Denise M.; Domingues, Betânia L. T. B.; Peres, Jaqueline C.; Araújo, Aderson S.; Costa, Fernando F.; Sonati, Maria F.

Source: European Journal of Haematology, Volume 83, Number 4, October 2009 , pp. 378-382(5)

Publisher: Blackwell Publishing

Characterisation of the British α⁰-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada

Authors: Eng, Barry; Greenlay, Benjamin; Waye, John S.

Source: British Journal of Haematology, Volume 147, Number 1, October 2009 , pp. 150-152(3)

Publisher: Blackwell Publishing

OP19.05: Is middle cerebral artery Doppler useful in the prenatal prediction of homozygous α⁰-thalassaemia?

Authors: Leung, K. Y.; Cheong, K.; Lee, C. P.; Chan, V.; Lam, Y. H.; Tang, H. Y.

Source: Ultrasound in Obstetrics and Gynecology, Volume 34, Supplement 1, September 2009 , pp. 122-122(1)

Publisher: John Wiley & Sons, Ltd.

Evaluating five dedicated automatic devices for haemoglobinopathy diagnostics in multi-ethnic populations

Authors: VAN DELFT, P.; LENTERS, E.; BAKKER-VERWEIJ, M.; deKORTE, M.; BAYLAN, U.; HARTEVELD, C. L.; GIORDANO, P. C.

Source: International Journal of Laboratory Hematology, Volume 31, Number 5, October 2009 , pp. 484-495(12)

Publisher: Blackwell Publishing

Red blood cell microcytosis and hypochromia in the differential diagnosis of iron deficiency and β-thalassaemia trait

Author: URRECHAGA, E.

Source: International Journal of Laboratory Hematology, Volume 31, Number 5, October 2009 , pp. 528-534(7)

Publisher: Blackwell Publishing

Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North America

Authors: Vogiatzi, Maria G.; Macklin, Eric A.; Trachtenberg, Felicia L.; Fung, Ellen B.; Cheung, Angela M.; Vichinsky, Elliott; Olivieri, Nancy; Kirby, Melody; Kwiatkowski, Janet L.; Cunningham, Melody; Holm, Ingrid A.; Fleisher, Martin; Grady, Robert W.; Peterson, Charles M.; Giardina, Patricia J.

Source: British Journal of Haematology, Volume 146, Number 5, September 2009 , pp. 546-556(11)

Publisher: Blackwell Publishing

Increased erythropoiesis of β-thalassaemia/Hb E proerythroblasts is mediated by high basal levels of ERK1/2 activation

Authors: Wannatung, Tirawat; Lithanatudom, Pathrapol; Leecharoenkiat, Amporn; Svasti, Saovaros; Fucharoen, Suthat; Smith, Duncan R.

Source: British Journal of Haematology, Volume 146, Number 5, September 2009 , pp. 557-568(12)

Publisher: Blackwell Publishing

Levels of non-transferrin-bound iron as an index of iron overload in patients with thalassaemia intermedia

Authors: Taher, Ali; Musallam, Khaled M.; El Rassi, Fouad; Duca, Lorena; Inati, Adlette; Koussa, Suzane; Cappellini, Maria D.

Source: British Journal of Haematology, Volume 146, Number 5, September 2009 , pp. 569-572(4)

Publisher: Blackwell Publishing

Pseudoxanthoma elasticum-like lesions in association with thalassaemia major

Authors: Yu, Shirley; Ming, Andrew; Wegman, Annette

Source: Australasian Journal of Dermatology, Volume 50, Number 3, August 2009 , pp. 186-189(4)

Publisher: Blackwell Publishing