Estonia (EE)

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

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Abstract

Journal

2019 ESC guidelines for the diagnosis and management of chronic coronary syndromes (2020) Knuuti J, Wijns W, Achenbach S, Agewall S, Barbato E, Bax JJ, Capodanno D, et al. Journal article, Review article Natural clusters of tuberous sclerosis complex (TSC)-associated neuropsychiatric disorders (TAND): new findings from the TOSCA TAND research project. (2020) De Vries PJ, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, D'Amato L, et al. Journal article New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics (2020) Begemann A, Sticht H, Begtrup A, Vitobello A, Faivre L, Banka S, Alhaddad B, et al. Journal article Quantitative analysis of fluorescent ligand binding to dopamine D3 receptors using live cell microscopy (2020) Allikalt A, Laasfeld T, Ilisson M, Kopanchuk S, Rinken A Journal article ETSI SmartBAN Architecture: The Global Vision for Smart Body Area Networks (2020) Hamalainen M, Mucchi L, Girod-Genet M, Paso T, Farserotu J, Tanaka H, Anzai D, et al. Journal article Influence of carboxylate anions on phase behavior of choline ionic liquid mixtures (2020) Elhi F, Gantman M, Nurk G, Schulz P, Wasserscheid P, Aabloo A, Põhako-Esko K Journal article Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis (2020) Frey S, Sticht H, Wilsmann-Theis D, Gerschütz A, Wolf K, Löhr S, Haskamp S, et al. Journal article CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Caliebe A, Nagel I, Young D, Horvath G, Santoro SL, et al. Journal article CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum (2019) Konrad E, Nardini N, Blyth M, Prescott K, Bouman AM, Brilstra EH, Caliebe A, et al. Conference contribution Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures (2019) Zweier M, Begemann A, Mcwalter K, Cho MT, Abela L, Banka S, Behring B, et al. Conference contribution