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Susanne Rinné

*born* 1978 *in* Gießen
Ingenieurin

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Diss. Fachbereich Medizin, Univ. Marburg

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Molecular mechanism of autosomal recessive long QT-syndrome 1 without deafness

Oertli, Annemarie (Verfasser)

International journal of molecular sciences. - Basel : Molecular Diversity Preservation International, 2000-. - Online-Ressource. - ISSN 1422-0067. - Band 22 (2021), Seite 1-13, Artikel-ID: 1112

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Molecular mechanism of autosomal eecessive long QT-syndrome 1 without deafness

Oertli, Annemarie (Verfasser)

Freiburg : Universität, 2021

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Rational design, synthesis, and evaluation of novel polypharmacological compounds targeting NaV1.5, KV1.5, and K2P channels for atrial fibrillation

Camargo-Ayala, Lorena (Verfasser)

Freiburg : Universität, 2025

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Hyperinsulinemic Hypoglycemia Associated with a CaV1.2 Variant with Mixed Gain- and Loss-of-Function Effects

Kummer, Sebastian (Verfasser)

Marburg : Philipps-Universität Marburg, 2023

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Hyperinsulinemic hypoglycemia associated with a CaV1.2 variant with mixed gain- and loss-of-function effects

Kummer, Sebastian (Verfasser)

Freiburg : Universität, 2022

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New Cav1.2 channelopathy with high-functioning autism, affective disorder, severe dental enamel defects, a short QT interval, and a novel CACNA1C loss-of-function mutation

Endres, Dominique (Verfasser)

Freiburg : Universität, 2020

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Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia

Decher, Niels (Verfasser)

Freiburg : Universität, 2019

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Susanne Rinné

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