Hereditary Hemochromatosis (HFE) genotypes in heart failure: Relation to etiology and prognosis
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Hereditary Hemochromatosis (HFE) genotypes in heart failure: Relation to etiology and prognosis ; volume:11 ; number:1 ; day:29 ; month:7 ; year:2010 ; pages:1-7 ; date:12.2010
BMC medical genetics ; 11, Heft 1 (29.7.2010), 1-7, 12.2010
- Contributor
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Møller, Daniel V.
Pecini, Redi
Gustafsson, Finn
Hassager, Christian
Hedley, Paula
Jespersgaard, Cathrine
Torp-Pedersen, Christian
Christiansen, Michael
Køber, Lars V.
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-11-117
- URN
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urn:nbn:de:1111-2016071512386
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:54 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Møller, Daniel V.
- Pecini, Redi
- Gustafsson, Finn
- Hassager, Christian
- Hedley, Paula
- Jespersgaard, Cathrine
- Torp-Pedersen, Christian
- Christiansen, Michael
- Køber, Lars V.
- SpringerLink (Online service)
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Developing and improving genome editing as a therapeutic tool for hereditary hemochromatosis
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Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China
2039 T2* CMR in hereditary hemochromatosis
Hypogonadotropic hypogonadism in men with hereditary hemochromatosis
Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis
Hepcidin knockout mice constitute a suitable mouse model for hereditary hemochromatosis
Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications
Analysis of natural killer cell functions in patients with hereditary hemochromatosis
Developing and improving genome editing as a therapeutic tool for hereditary hemochromatosis
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
Analysis of hand joint space morphology in women and men with hereditary hemochromatosis
Analysis of Hand Joint Space Morphology in Women and Men with Hereditary Hemochromatosis
Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China
2039 T2* CMR in hereditary hemochromatosis
Hypogonadotropic hypogonadism in men with hereditary hemochromatosis
Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis
Hepcidin knockout mice constitute a suitable mouse model for hereditary hemochromatosis
Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications
Analysis of natural killer cell functions in patients with hereditary hemochromatosis
Developing and improving genome editing as a therapeutic tool for hereditary hemochromatosis
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis
Analysis of hand joint space morphology in women and men with hereditary hemochromatosis
Analysis of Hand Joint Space Morphology in Women and Men with Hereditary Hemochromatosis
Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data