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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|March 23, 2015
Radiosensitization of NSCLC cells by EGFR inhibition is the result of an enhanced p53-dependent G1 arrestMalte Kriegs, Kristin Gurtner, Yildiz Can, et al.Journal of Minimally Invasive Gynecology|July 1, 2021
Superior Hypogastric Plexus Nerve Block in Minimally Invasive Gynecology: A Randomized Controlled TrialPraveen De Silva, Sam Daniels, Mujahid Emad Bukhari, et al.Dental Traumatology : Official Publication of International Association for Dental Traumatology|January 22, 2010
Impact energy absorption of three mouthguard materials in three environmentsDarin R Lunt, Deborah A Mendel, William A Brantley, et al.Clinical Nuclear Medicine|October 25, 2016
First Experience With SPECT/CT Using a 99mTc-Labeled Inhibitor for Prostate-Specific Membrane Antigen in Patients With Biochemical Recurrence of Prostate CancerJulia Reinfelder, Torsten Kuwert, Michael Beck, et al.Journal of Neurology|March 3, 2006
Pattern of microstructural brain tissue alterations in Fabry disease: a diffusion-tensor imaging studyAndreas Fellgiebel, Martin Mazanek, Catharina Whybra, et al.Drug Design, Development and Therapy|November 22, 2019
Cardio- Renal Outcomes With Long- Term Agalsidase Alfa Enzyme Replacement Therapy: A 10- Year Fabry Outcome Survey (FOS) AnalysisUma Ramaswami, Michael Beck, Derralynn Hughes, et al.Molecular Genetics and Metabolism|September 15, 2019
Founder effect of Fabry disease due to p.F113L mutation: Clinical profile of a late-onset phenotypeOlga Azevedo, Andreas Gal, Rui Faria, et al.Human Molecular Genetics|June 18, 2011
Ccdc66 null mutation causes retinal degeneration and dysfunctionWanda M Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, et al.American Journal of Human Genetics|August 14, 2010
Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosaThomas Langmann, Silvio Alessandro Di Gioia, Isabella Rau, et al.Pageof 31