Literature DB >> 13906009

[Congenital atransferrinemia].

L HEILMEYER, W KELLER, O VIVELL, K BETKE, F WOEHLER, W KEIDERLING.   

Abstract

Entities:  

Keywords:  TRANSFERRIN/deficiency

Mesh：

Substances：

Year:  1961        PMID： 13906009

Source DB:  PubMed          Journal:  Schweiz Med Wochenschr        ISSN： 0036-7672


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  3 in total

1.  Congenital Hypotransferrinemia, an Unusual Cause of Iron Deficiency Anemia: Report of Two Cases.

Authors:  Dinesh Chandra; Bhavna Dhingra; Tulika Seth; Pravas Mishra; Divya Bansal; Manoranjan Mahapatra; H P Pati
Journal:  Indian J Hematol Blood Transfus       Date:  2016-11-16       Impact factor: 0.900

2.  Hyperferritinemia without iron overload in patients with bilateral cataracts: a case series.

Authors:  Arne Kröger; Esther B Bachli; Andrew Mumford; Christoph Gubler
Journal:  J Med Case Rep       Date:  2011-09-21

Review 3.  Ferroportin disease: pathogenesis, diagnosis and treatment.

Authors:  Antonello Pietrangelo
Journal:  Haematologica       Date:  2017-11-03       Impact factor: 9.941
  3 in total

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