Universität zu Köln

University / College


Location: Köln, Germany (DE) DE

ISNI: 0000000085803777

ROR: https://ror.org/00rcxh774

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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Unpublished / Preprint

Publication year

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To

Abstract

Journal

Symptoms, disease severity and treatment of adults with a new diagnosis of severe aortic stenosis (2019) Frey N, Steeds RP, Rudolph TK, Thambyrajah J, Serra A, Schulz E, Maly J, et al. Journal article Positron Emission Tomography-Guided Treatment in Early-Stage Favorable Hodgkin Lymphoma: Final Results of the International, Randomized Phase III HD16 Trial by the German Hodgkin Study Group (2019) Fuchs M, Goergen H, Kobe C, Kuhnert G, Lohri A, Greil R, Sasse S, et al. Journal article Association of Surgical Hematoma Evacuation vs Conservative Treatment With Functional Outcome in Patients With Cerebellar Intracerebral Hemorrhage (2019) Kuramatsu J, Biffi A, Gerner S, Sembill J, Sprügel M, Leasure A, Sansing L, et al. Journal article Incidence and outcome of peri-procedural transcatheter heart valve embolization and migration: the TRAVEL registry (TranscatheteR HeArt Valve EmboLization and Migration) (2019) Kim WK, Schäfer U, Tchetche D, Nef H, Avanzas P, Rudolph T, Scholtz S, et al. Journal article Lack of a Retinal Phenotype in a Syne-2/Nesprin-2 Knockout Mouse Model (2019) Falk N, Joachimsthaler A, Keßler K, Lux U, Noegel AA, Kremers J, Brandstätter JH, Gießl A Journal article Facilitated Data Relay and Effects on Treatment of Severe Aortic Stenosis in Europe (2019) Steeds RP, Lutz M, Thambyrajah J, Serra A, Schulz E, Maly J, Aiello M, et al. Journal article Whole-exome sequencing and large-scale re-sequencing in nonsyndromic cleft lip with/without cleft palate identify novel susceptibility genes (2019) Ishorst N, Henschel L, Thieme F, Drichel D, Sivalingam S, Mehrem SL, Fechtner AC, et al. Conference contribution Disruptive recessive TTN missense mutations cause a wide range of clinico-pathological features (2019) Rees M, Fukuzawa A, Nikoopour R, Kho A, Qi J, Fernandez-Garcia M, Wraige E, et al. Conference contribution Sarcomeric pathology induced by homozygous expression of the myofibrillar myopathy - associated p.W2711X filamin C mutant (2019) Schuld J, Orfanos Z, Chevessier F, Unger A, Kirfel G, Van Der Ven P, Linke W, et al. Conference contribution Imbalances in protein homeostasis caused by mutant desmin (2019) Clemen C, Winter L, Unger A, Berwanger C, Spörrer M, Linke W, Schröder R Conference contribution