Literature DB >> 4164467

Iron distribution in the liver of patients with thalassaemia major.

C L Berry, W C Marshall.   

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Year:  1967        PMID： 4164467     DOI： 10.1016/s0140-6736(67)91543-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  Absorption of inorganic and food iron in children with heterozygous and homozygous beta-thalassemia.

Authors:  H C Heinrich; E E Gabbe; K H Oppitz; D H Whang; C Bender-Götze; K H Schäfer; W Schröter; A A Pfau
Journal:  Z Kinderheilkd       Date:  1973-08-09

2.  Patterns of liver iron accumulation in patients with sickle cell disease and thalassemia with iron overload.

Authors:  Jane S Hankins; Matthew P Smeltzer; M Beth McCarville; Banu Aygun; Claudia M Hillenbrand; Russell E Ware; Mihaela Onciu
Journal:  Eur J Haematol       Date:  2010-03-31       Impact factor: 2.997

3.  Long-term chelation therapy in thalassaemia major: effect on liver iron concentration, liver histology, and clinical progress.

Authors:  M Barry; D M Flynn; E A Letsky; R A Risdon
Journal:  Br Med J       Date:  1974-04-06

4.  Liver in haemoglobin H disease.

Authors:  C B Keng; T K Khoo
Journal:  Gut       Date:  1970-05       Impact factor: 23.059

5.  Hemochromatosis caused by excessive vitamin iron intake.

Authors:  G R Hennigar; W B Greene; E M Walker; C de Saussure
Journal:  Am J Pathol       Date:  1979-08       Impact factor: 4.307
  5 in total

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