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Publisher : blackwell

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Ferritin heavy/light chain (FTH1/FTL) expression, serum ferritin levels, and their functional as well as prognostic roles in acute myeloid leukemia.

Authors : Bertoli S; Service d'Hématologie, Centre Hospitalier Universitaire de Toulouse, Institut Universitaire du Cancer de Toulouse Oncopole, Toulouse, France.; Université Toulouse III Paul Sabatier, Toulouse, France.

Subjects: Gene Expression Regulation, Leukemic*; Apoferritins/Apoferritins/Apoferritins/*genetics ; Ferritins/Ferritins/Ferritins/*blood

Source: European journal of haematology [Eur J Haematol] 2019 Feb; Vol. 102 (2), pp. 131-142. Date of Electronic Publication: 2018 Nov 28.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium:

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Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron deficiency anemia associated with a new mutation in the iron responsive element of the L ferritin gene in a Swiss family.

Authors : Rüfer A; Division of Hematology and Central Hematology Laboratory, Kantonsspital, Luzern, Switzerland. ; Howell JP

Subjects: Mutation*; Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/*etiology ; Apoferritins/Apoferritins/Apoferritins/*genetics Hyperferritinemia, hereditary, with congenital cataracts

Source: European journal of haematology [Eur J Haematol] 2011 Sep; Vol. 87 (3), pp. 274-8. Date of Electronic Publication: 2011 Apr 06.Publisher: Blackwell Country of Publication: England NLM ID: 8703985 Publication Model: Print-Electronic Cited Medium:

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