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NPJ Parkinson'S Disease|June 12, 2025
Longitudinal assessment of the association between pesticide exposure and lifestyle with Parkinson's disease motor severityTheresa Lüth, Amke Caliebe, Carolin Gabbert, et al.
International Journal of Oral and Maxillofacial Surgery|July 31, 2018
Tongue reduction in Beckwith-Wiedemann syndrome: outcome and treatment algorithmH Naujokat, B Möller, H Terheyden, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Genetic investigation of FOXO3A requires special attention due to sequence homology with FOXO3BFriederike Flachsbart, Michael Möller, Carolin Däumer, et al.
Anaesthesia|February 14, 2012
A comparison of the Nexfin® and transcardiopulmonary thermodilution to estimate cardiac output during coronary artery surgeryO Broch, J Renner, M Gruenewald, et al.
Frontiers in Oncology|June 13, 2022
Case Report: <i>GNAQ</i>- and <i>SF3B1</i> Mutations in an Aggressive Case of Relapsing Uveal Ring MelanomaMichelle Prasuhn, Josephine Christin Freitag, Sabine Lüken, et al.
Therapeutic Drug Monitoring|October 2, 2014
Which Genetic Determinants Should be Considered for Tacrolimus Dose Optimization in Kidney Transplantation? A Combined Analysis of Genes Affecting the CYP3A LocusHenrike Bruckmueller, Anneke Nina Werk, Lutz Renders, et al.
European Journal of Medical Genetics|March 3, 2011
A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson-Golabi-Behmel syndrome Report, antenatal findings and reviewJan Weichert, Andreas Schröer, Feriel Amari, et al.
Molecular Syndromology|April 19, 2012
Novel Tandem Duplication in Exon 1 of the SNURF/SNRPN Gene in a Child with Transient Excessive Eating Behaviour and Weight GainS Naik, N S Thomas, J H Davies, et al.
Anesthesia and Analgesia|December 15, 2017
Videolaryngoscopy for Physician-Based, Prehospital Emergency Intubation: A Prospective, Randomized, Multicenter Comparison of Different Blade Types Using A.P. Advance, C-MAC System, and KingVisionErol Cavus, Sebastian Janssen, Florian Reifferscheid, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Phenotypical variation in cousins with the identical partial trisomy 9 (pter-q22.2) and 7 (q35-qter) at 16 and 23 weeks gestationS Metzke-Heidemann, H Kuhling-von Kaisenberg, A Caliebe, et al.
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