Literature DB >> 19787795

Hemoglobin H-constant spring in North America: an alpha thalassemia with frequent complications.

Sylvia Titi Singer, Hae-Young Kim, Nancy F Olivieri, Janet L Kwiatkowski, Thomas D Coates, Susan Carson, Ellis Neufeld, Melody J Cunningham, Patricia J Giardina, Brigitta U Mueller, Charles T Quinn, Ellen Fung, Elliott Vichinsky.   

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Year:  2009        PMID： 19787795      PMCID： PMC4254706          DOI： 10.1002/ajh.21523

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  20 in total

1.  Serum ferritin underestimates liver iron concentration in transfusion independent thalassemia patients as compared to regularly transfused thalassemia and sickle cell patients.

Authors:  Zahra Pakbaz; Roland Fischer; Ellen Fung; Peter Nielsen; Paul Harmatz; Elliott Vichinsky
Journal:  Pediatr Blood Cancer       Date:  2007-09       Impact factor: 3.167

2.  Prevalence of fractures among the Thalassemia syndromes in North America.

Authors:  M G Vogiatzi; E A Macklin; E B Fung; E Vichinsky; N Olivieri; J Kwiatkowski; A Cohen; E Neufeld; P J Giardina
Journal:  Bone       Date:  2005-11-17       Impact factor: 4.398

3.  Qualitative and quantitative magnetic resonance imaging in haemoglobin H disease: screening for iron overload.

Authors:  G C Ooi; F E Chen; K N Chan; K W Tsang; Y H Wong; R Liang; V Chan; H Ngan
Journal:  Clin Radiol       Date:  1999-02       Impact factor: 2.350

4.  Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.

Authors:  R Origa; M C Sollaino; N Giagu; S Barella; S Campus; C Mandas; P Bina; L Perseu; R Galanello
Journal:  Br J Haematol       Date:  2006-11-27       Impact factor: 6.998

5.  Use of the oral chelator deferiprone in the treatment of iron overload in patients with Hb H disease.

Authors:  Joyce C W Chan; Chor-Sang Chim; Clara G C Ooi; Bernard Cheung; Raymond Liang; Tai-Kwong Chan; Vivian Chan
Journal:  Br J Haematol       Date:  2006-04       Impact factor: 6.998

6.  Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes.

Authors:  C Camaschella; S Gonella; R Calabrese; F Vischia; A Roetto; G Graziadei; U Mazza; M D Cappellini
Journal:  Haematologica       Date:  1996 Sep-Oct       Impact factor: 9.941

7.  Lipid profile in beta-thalassemia intermedia patients: correlation with erythroid bone marrow activity.

Authors:  G Amendola; P Danise; N Todisco; G D'Urzo; A Di Palma; R Di Concilio
Journal:  Int J Lab Hematol       Date:  2007-06       Impact factor: 2.877

8.  Erythroid marrow activity and hemoglobin H levels in hemoglobin H disease.

Authors:  I Papassotiriou; J Traeger-Synodinos; E Kanavakis; M Karagiorga; A Stamoulakatou; C Kattamis
Journal:  J Pediatr Hematol Oncol       Date:  1998 Nov-Dec       Impact factor: 1.289

9.  Venous thrombosis in haemoglobin H disease after splenectomy.

Authors:  S C Tso; T K Chan; D Todd
Journal:  Aust N Z J Med       Date:  1982-12

10.  Hb Constant Spring [alpha 142, Term-->Gln (TAA>CAA in alpha2)] in the alpha-thalassemia of anemic patients in Myanmar.

Authors:  Keiko Harano; Teruo Harano; Shigeru Okada
Journal:  Hemoglobin       Date:  2008       Impact factor: 0.849
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  3 in total

Review 1.  Clinical manifestations of α-thalassemia.

Authors:  Elliott P Vichinsky
Journal:  Cold Spring Harb Perspect Med       Date:  2013-05-01       Impact factor: 6.915

Review 2.  Non-transfusion-dependent thalassemias.

Authors:  Khaled M Musallam; Stefano Rivella; Elliott Vichinsky; Eliezer A Rachmilewitz
Journal:  Haematologica       Date:  2013-06       Impact factor: 9.941

3.  Prolonged Pyrexia: Kikuchi-Fujimoto Disease in a Patient With Hb H-Constant Spring Thalassemia.

Authors:  Ganesh Kasinathan
Journal:  Clin Med Insights Case Rep       Date:  2020-06-26
  3 in total

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