Clinical and molecular genetic characterization of patients with familial hypercholesterolemia
- Weitere Titel
-
Klinische und molekulargenetische Charakterisierung von Patient*innen mit Familiärer Hypercholesterinämie
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Deutsch
- Anmerkungen
-
Berlin, Medizinische Fakultät Charité - Universitätsmedizin Berlin, Dissertation, 2022
- Schlagwort
-
Humboldt-Universität zu Berlin. Medizinische Fakultät (Charité)
Primäre Hypercholesterinämie
Patient
Genmutation
Risikofaktor
Molekulargenetik
- Ereignis
-
Veröffentlichung
- (wo)
-
Berlin
- (wer)
-
Medizinische Fakultät Charité - Universitätsmedizin Berlin
- (wann)
-
2022
- Urheber
- DOI
-
10.17169/refubium-34167
- URN
-
urn:nbn:de:kobv:188-refubium-34449-8
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:27 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Rieck, Lorenz
- Medizinische Fakultät Charité - Universitätsmedizin Berlin
Entstanden
- 2022
Ähnliche Objekte (12)
Genetic Testing in Familial Hypercholesterolemia: Is It for Everyone?
Familial Hypercholesterolemia: new therapeutic approaches
Sex Differences in Familial Hypercholesterolemia
Familial Hypercholesterolemia: Present and Future Management
The Clinical Importance of Differentiating Monogenic Familial Hypercholesterolemia from Polygenic Hypercholesterolemia
SORBS2 as a molecular target for atherosclerosis in patients with familial hypercholesterolemia
Current causes of death in familial hypercholesterolemia
Familial hypercholesterolemia in very young myocardial infarction
Deploying Clinical Decision Support for Familial Hypercholesterolemia
Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank
An update on lipid apheresis for familial hypercholesterolemia
Genetic Testing in Familial Hypercholesterolemia: Is It for Everyone?
Familial Hypercholesterolemia: new therapeutic approaches
Sex Differences in Familial Hypercholesterolemia
Familial Hypercholesterolemia: Present and Future Management
The Clinical Importance of Differentiating Monogenic Familial Hypercholesterolemia from Polygenic Hypercholesterolemia
SORBS2 as a molecular target for atherosclerosis in patients with familial hypercholesterolemia
Current causes of death in familial hypercholesterolemia
Familial hypercholesterolemia in very young myocardial infarction
Deploying Clinical Decision Support for Familial Hypercholesterolemia
Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank
An update on lipid apheresis for familial hypercholesterolemia
Genetic Testing in Familial Hypercholesterolemia: Is It for Everyone?
Familial Hypercholesterolemia: new therapeutic approaches
Sex Differences in Familial Hypercholesterolemia
Familial Hypercholesterolemia: Present and Future Management
The Clinical Importance of Differentiating Monogenic Familial Hypercholesterolemia from Polygenic Hypercholesterolemia
SORBS2 as a molecular target for atherosclerosis in patients with familial hypercholesterolemia
Current causes of death in familial hypercholesterolemia
Familial hypercholesterolemia in very young myocardial infarction
Deploying Clinical Decision Support for Familial Hypercholesterolemia
Fast and Easy Nanopore Sequencing Workflow for Rapid Genetic Testing of Familial Hypercholesterolemia
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobank