Egypt (EG)

Antibacterial activity and biocompatibility of zein scaffolds containing silver-doped bioactive glass (2018) El-Rashidy AA, Waly G, Gad A, Roether J, Hum J, Yang Y, Detsch R, et al. Journal article, Original article Fatty Lesions Detected on MRI Scans in Patients with Ankylosing Spondylitis Are Based on the Deposition of Fat in the Vertebral Bone Marrow (2018) Baraliakosi X, Boehm H, Samir A, Schett G, Braun J, Ramming A Conference contribution FATTY LESIONS DETECTED ON MRI SCANS IN PATIENTS WITH ANKYLOSING SPONDYLITIS ARE BASED ON THE DEPOSITION OF FAT IN THE VERTEBRAL BONE MARROW (2018) Baraliakos X, Boehm H, Barakat AS, Schett G, Braun J Conference contribution Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care (2018) Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, et al. Journal article The p.Arg435His Variation of IgG3 With High Affinity to FcRn Is Associated With Susceptibility for Pemphigus Vulgaris-Analysis of Four Different Ethnic Cohorts (2018) Recke A, Konitzer S, Lemcke S, Freitag M, Sommer NM, Abdelhady M, Amoli MM, et al. Journal article Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome (2017) Rao J, Ashraf S, Tan W, Van Der Ven AT, Gee HY, Braun DA, Feher K, et al. Journal article Dynamic Docking and Undocking Processes Addressing Selectively the Outside and Inside of Polymersomes (2017) Iyisan B, Siedel AC, Gumz H, Yassin M, Kluge J, Gaitzsch J, Formanek P, et al. Journal article “Isolated” DyO+ Embedded in a Ceramic Apatite Matrix Featuring Single-Molecule Magnet Behavior with a High Energy Barrier for Magnetization Relaxation (2017) Kazin PE, Zykin MA, Utochnikova VV, Magdysyuk OV, Vasiliev AV, Zubavichus YV, Schnelle W, et al. Journal article Panobinostat plus bortezomib and dexamethasone: impact of dose intensity and administration frequency on safety in the PANORAMA 1 trial (2017) San-Miguel JF, Hungria VTM, Yoon SS, Beksac M, Dimopoulos MA, Elghandour A, Jedrzejczak WW, et al. Journal article Mutations in KEOPS-complex genes cause nephritic syndrome with primary microcephaly (2017) Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, et al. Journal article