Literature DB >> 24370385

Monitoring of hepcidin levels in a patient with G80S-linked ferroportin disease undergoing iron depletion by phlebotomy.

Fleur Wolff1, Benjamin Bailly2, Béatrice Gulbis3, Frédéric Cotton3.   

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Year:  2013        PMID： 24370385     DOI： 10.1016/j.cca.2013.12.024

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  4 in total

1.  Detection of a rare mutation in the ferroportin gene through targeted next generation sequencing.

Authors:  Ludovica Ferbo; Paola M Manzini; Sadaf Badar; Natascia Campostrini; Alberto Ferrarini; Massimo Delledonne; Tiziana Francisci; Valter Tassi; Adriano Valfrè; Anna M Dall'omo; Sergio D'antico; Domenico Girelli; Antonella Roetto; Marco De Gobbi
Journal:  Blood Transfus       Date:  2016-04-28       Impact factor: 3.443

2.  Human macrophage ferroportin biology and the basis for the ferroportin disease.

Authors:  Manuela Sabelli; Giuliana Montosi; Cinzia Garuti; Angela Caleffi; Stefania Oliveto; Stefano Biffo; Antonello Pietrangelo
Journal:  Hepatology       Date:  2017-03-22       Impact factor: 17.425

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

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

Review 4.  Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features.

Authors:  L Tom Vlasveld; Roel Janssen; Edouard Bardou-Jacquet; Hanka Venselaar; Houda Hamdi-Roze; Hal Drakesmith; Dorine W Swinkels
Journal:  Pharmaceuticals (Basel)       Date:  2019-09-09
  4 in total

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