Universitätsklinikum Düsseldorf

Hospital


Location: Düsseldorf, Germany (DE) DE

ISNI: 0000000089227789

ROR: https://ror.org/006k2kk72

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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Unpublished / Preprint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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Abstract

Journal

Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration (2020) Fagerberg CR, Taylor A, Distelmaier F, Schrøder HD, Kibæk M, Wieczorek D, Tarnopolsky M, et al. Journal article Commercially Available Gene Expression Assays as Predictive Tools for Adjuvant Radiotherapy? A Critical Review (2020) Krug D, Baumann R, Budach W, Duma MN, Dunst J, Feyer P, Fietkau R, et al. Journal article Repeated kidney re-transplantation—the Eurotransplant experience: a retrospective multicenter outcome analysis (2020) Assfalg V, Selig K, Tolksdorf J, Van Meel M, De Vries E, Ramsoebhag AM, Rahmel A, et al. Journal article The 27th annual meeting of the working group kidney transplantation of the German Society for Urology November 21-24, 2019 in Halle (Saale) (2019) Weigand K, Friedersdorff F, Apel H, Stoeckle M, Putz J, Dreikorn K, Giessing M, Fornara P Journal article, Editorial Translational Highlights in Breast and Ovarian Cancer 2019 – Immunotherapy, DNA Repair, PI3K Inhibition and CDK4/6 Therapy (2019) Hartkopf AD, Mueller V, Woeckel A, Lux MP, Janni W, Ettl J, Belleville E, et al. Journal article, Review article Between quarrel and strife: controversies in emergency medicine Zwischen Zank und Zwist: Kontroversen in der Notfallmedizin (2019) Bernhard M, Dormann H, Waydhas C Journal article Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis (2019) Gravesande KSV, Blaschek A, Calabrese P, Rostasy K, Huppke P, Kessler JJ, Kalbe E, et al. Journal article De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures (2019) Horn S, Au M, Basel-Salmon L, Bayrak-Toydemir P, Chapin A, Cohen L, Elting MW, et al. Journal article The preleukemic TCF3-PBX1 gene fusion can be generated in utero and is present in ≈0.6% of healthy newborns (2019) Hein D, Dreisig K, Metzler M, Izraeli S, Schmiegelow K, Borkhardt A, Fischer U Journal article Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly (2019) Richard EM, Polla DL, Assir MZ, Contreras M, Shahzad M, Khan AA, Razzaq A, et al. Journal article