Literature DB >> 4690069

Hereditary spherocytosis, haemochromatosis, diabetes mellitus and chondrocalcinosis.

E M Berry, J P Miller.   

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Year:  1973        PMID： 4690069      PMCID： PMC1644394     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  3 in total

1.  Studies on congenital hemolytic syndromes, IV. Gastrointestinal absorption of iron.

Authors:  M E ERLANDSON; B WALDEN; G STERN; M W HILGARTNER; J WEHMAN; C H SMITH
Journal:  Blood       Date:  1962-03       Impact factor: 22.113

2.  Hereditary spherocytosis with secondary haemochromatosis.

Authors:  M Barry; P J Scheuer; S Sherlock; C F Ross; R Williams
Journal:  Lancet       Date:  1968-08-31       Impact factor: 79.321

3.  Hemochromatosis in association with hereditary spherocyto- sis.

Authors:  J D Wilson; P J Scott; J D North
Journal:  Arch Intern Med       Date:  1967-12
  3 in total
  4 in total

Review 1.  Genetic haemochromatosis.

Authors:  A B Bomford; I W Dymock; E B Hamilton
Journal:  Gut       Date:  1991-09       Impact factor: 23.059

Review 2.  Iron and the liver.

Authors:  M Barry
Journal:  Gut       Date:  1974-04       Impact factor: 23.059

3.  Patients with hereditary spherocytosis may have clinically significant iron overload when they are also heterozygous for hemochromatosis.

Authors:  D N Mohler; M S Wheby
Journal:  Trans Am Clin Climatol Assoc       Date:  1985

4.  Sideroblastic anaemia with iron overload presenting as an arthropathy.

Authors:  M A Fitzcharles; J R Kirwan; B T Colvin; H L Currey
Journal:  Ann Rheum Dis       Date:  1982-02       Impact factor: 19.103
  4 in total

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