Chelating Polymers for Hereditary Hemochromatosis Treatment-Reference-Cited by-同舟云学术

Chelating Polymers for Hereditary Hemochromatosis Treatment

Published:2020-09-21 Issue:12 Volume:20 Page:2000254
ISSN:1616-5187
Container-title:Macromolecular Bioscience
language:en
Short-container-title:Macromol. Biosci.

Author:

Groborz Ondřej¹²³,Poláková Lenka¹,Kolouchová Kristýna¹⁴,Švec Pavel¹⁴,Loukotová Lenka¹,Miriyala Vijay Madhav⁵,Francová Pavla⁶,Kučka Jan¹,Krijt Jan⁷,Páral Petr⁶,Báječný Martin⁶,Heizer Tomáš⁶,Pohl Radek⁵,Dunlop David⁵,Czernek Jiří¹,Šefc Luděk⁶,Beneš Jiří³,Štěpánek Petr¹,Hobza Pavel⁵^ORCID,Hrubý Martin¹^ORCID

Affiliation:

1. Institute of Macromolecular Chemistry Czech Academy of Sciences Heyrovského náměstí 2 162 06 Prague 6 Czech Republic

2. Department of Organic Chemistry Faculty of Science Charles University Hlavova 8 128 43 Prague 2 Czech Republic

3. Institute of Biophysics and Informatics First Faculty of Medicine Charles University Salmovská 1 120 00 Prague 2 Czech Republic

4. Department of Physical Chemistry Faculty of Science Charles University Hlavova 8 128 43 Prague 2 Czech Republic

5. Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Flemingovo náměstí 542/2 162 06 Prague 6 Czech Republic

6. Center for Advanced Preclinical Imaging (CAPI) First Faculty of Medicine Charles University Salmovská 3 120 00 Prague 2 Czech Republic

7. Institute of Pathophysiology First Faculty of Medicine Charles University U Nemocnice 5 128 53 Prague 2 Czech Republic

Funder

European Regional Development Fund

Univerzita Karlova v Praze

Grantová Agentura, Univerzita Karlova

Ministerstvo Školství, Mládeže a Tělovýchovy

Grantová Agentura České Republiky

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Biomaterials,Bioengineering,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mabi.202000254

Reference58 articles.

1. Haemochromatosis

2. Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment

3. Haemochromatosis

4. Systematic Literature Review of the Burden of Disease and Treatment for Transfusion-dependent β-Thalassemia

5. Screening of Patients With Iron Overload to Identify Hemochromatosis and Porphyria Cutanea Tarda

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