Literature DB >> 23085251

Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation.

D J Smith, G J Anderson, I L Lamont, P Masel, S C Bell, D W Reid.   

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Year:  2012        PMID： 23085251     DOI： 10.1016/j.jcf.2012.10.001

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN： 1569-1993            Impact factor:   5.482


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  4 in total

1.  Iron supplementation does not worsen respiratory health or alter the sputum microbiome in cystic fibrosis.

Authors:  Alex H Gifford; Diana M Alexandru; Zhigang Li; Dana B Dorman; Lisa A Moulton; Katherine E Price; Thomas H Hampton; Mitchell L Sogin; Jonathan B Zuckerman; H Worth Parker; Bruce A Stanton; George A O'Toole
Journal:  J Cyst Fibros       Date:  2013-12-13       Impact factor: 5.482

Review 2.  Pregnancy and cystic fibrosis: Approach to contemporary management.

Authors:  James Geake; George Tay; Leonie Callaway; Scott C Bell
Journal:  Obstet Med       Date:  2014-11-07

3.  Serum Hepcidin Level as a Marker of Iron Status in Children with Cystic Fibrosis.

Authors:  Monika Kałużna-Czyż; Urszula Grzybowska-Chlebowczyk; Halina Woś; Sabina Więcek
Journal:  Mediators Inflamm       Date:  2018-07-02       Impact factor: 4.711

4.  Iron Deficiency in Cystic Fibrosis: A Cross-Sectional Single-Centre Study in a Referral Adult Centre.

Authors:  Hervé Lobbes; Stéphane Durupt; Sabine Mainbourg; Bruno Pereira; Raphaele Nove-Josserand; Isabelle Durieu; Quitterie Reynaud
Journal:  Nutrients       Date:  2022-02-05       Impact factor: 5.717
  4 in total

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