Britta Otte
3 Papers
Britta Otte is an academic researcher. The author has contributed to research in topics: Population & Medical history. The author has an hindex of 3, co-authored 3 publications.
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Papers
Pathogenic classification of LPL gene variants reported to be associated with LPL deficiency
Rute Rodrigues,Marta Artieda,Diego Tejedor,Antonio Martínez,Pavlina Konstantinova,Harald Petry,Christian Meyer,Deyanira Corzo,Claus Sundgreen,Hans U. Klor,Ioanna Gouni-Berthold,Sabine Westphal,Elisabeth Steinhagen-Thiessen,Ulrich Julius,Karl Winkler,Erik S.G. Stroes,Anja Vogt,Phillip Hardt,Heinrich Prophet,Britta Otte,Børge G. Nordestgaard,Samir S. Deeb,John D. Brunzell +22 more
TL;DR: The deleterious mutations associated with LPL deficiency will assist in the diagnosis and selection of patients as candidates for the presently approved LPL gene therapy.
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Lipid-modifying therapy and low-density lipoprotein cholesterol goal attainment in patients with familial hypercholesterolemia in Germany: The CaReHigh Registry.
Nina Schmidt,Alexander Dressel,Tanja B. Grammer,Ioanna Gouni-Berthold,Ulrich Julius,Ursula Kassner,Gerald Klose,Christel König,Wolfgang Koenig,Britta Otte,Klaus G. Parhofer,Wibke Reinhard,Ulrike Schatz,Heribert Schunkert,Elisabeth Steinhagen-Thiessen,Anja Vogt,Ulrich Laufs,Winfried März +17 more
TL;DR: PCSK9i treatment in addition to standard therapy allows attainment of target values in many patients with initially very high LDL-C, as well as in patients with pre-existing CVD.
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CaRe high – Cascade screening and registry for high cholesterol in Germany
Nina Schmidt,Tanja B. Grammer,Ioanna Gouni-Berthold,Ulrich Julius,Ursula Kassner,Gerald Klose,Christel König,Ulrich Laufs,Britta Otte,Elisabeth Steinhagen-Thiessen,Christoph Wanner,Winfried März +11 more
TL;DR: The cascade screening and registry for families of hereditary hypercholesterolemia (FH) is proposed in this article, which is an inherited disorder of the LDL metabolism, leading to cardiovascular disease.
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