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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Springe zu: 2022
Anzahl der Publikationen: 2
2022
Sanin, Veronika 
ORCID: https://orcid.org/0000-0001-5371-7230; Schmieder, Raphael; Ates, Sara; Schlieben, Lea Dewi; Wiehler, Jens; Sun, Ruoyu; Decker, Manuela; Sander, Michaela; Holdenrieder, Stefan; Kohlmayer, Florian; Friedmann, Anna; Mall, Volker; Feiler, Therese; Dreßler, Arne; Strom, Tim M; Prokisch, Holger; Meitinger, Thomas; Scheidt, Moritz von ORCID: https://orcid.org/0000-0001-7159-8271; Koenig, Wolfgang ORCID: https://orcid.org/0000-0002-2064-9603; Leipold, Georg und Schunkert, Heribert
(2022):
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
In: European Journal of Public Health, Bd. 32, Nr. 3: S. 422-428
[PDF, 894kB]
ORCID: https://orcid.org/0000-0001-5371-7230; Schmieder, Raphael; Ates, Sara; Schlieben, Lea Dewi; Wiehler, Jens; Sun, Ruoyu; Decker, Manuela; Sander, Michaela; Holdenrieder, Stefan; Kohlmayer, Florian; Friedmann, Anna; Mall, Volker; Feiler, Therese; Dreßler, Arne; Strom, Tim M; Prokisch, Holger; Meitinger, Thomas; Scheidt, Moritz von ORCID: https://orcid.org/0000-0001-7159-8271; Koenig, Wolfgang ORCID: https://orcid.org/0000-0002-2064-9603; Leipold, Georg und Schunkert, Heribert
(2022):
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
In: European Journal of Public Health, Bd. 32, Nr. 3: S. 422-428
[PDF, 894kB]
Sanin, Veronika; Schmieder, Raphael; Ates, Sara; Schlieben, Lea Dewi; Wiehler, Jens; Sun, Ruoyu; Decker, Manuela; Sander, Michaela; Holdenrieder, Stefan; Kohlmayer, Florian; Friedmann, Anna; Mall, Volker; Feiler, Therese; Dressler, Arne; Strom, Tim M.; Prokisch, Holger; Meitinger, Thomas; Scheidt, Moritz von; Koenig, Wolfgang; Leipold, Georg und Schunkert, Heribert
(2022):
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.
In: Medizinische Genetik, Bd. 34, Nr. 1: S. 41-51