Hacettepe University

Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease. (2018) Burgmaier K, Kunzmann K, Ariceta G, Bergmann C, Buescher AK, Burgmaier M, Dursun I, et al. Journal article MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia (2018) Germeshausen M, Ancliff P, Estrada J, Metzler M, Ponstingl E, Ruetschle H, Schwabe D, 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 European Heart Rhythm Association (EHRA)/European Association of Cardiovascular Prevention and Rehabilitation (EACPR) position paper on how to prevent atrial fibrillation endorsed by the Heart Rhythm Society (HRS) and Asia Pacific Heart Rhythm Society (APHRS) (2017) Gorenek B, Pelliccia A, Benjamin EJ, Boriani G, Crijns HJ, Fogel RI, Van Gelder IC, et al. Journal article, Review article Subependymal giant cell astrocytomas in Tuberous Sclerosis Complex have consistent TSC1/TSC2 biallelic inactivation, and no BRAF mutations (2017) Bongaarts A, Giannikou K, Reinten RJ, Anink JJ, Mills JD, Jansen FE, Spliet WGM, et al. Journal article Ablation-cooled material removal with ultrafast bursts of pulses (2016) Kerse C, Kalaycıoğlu H, Elahi P, Çetin B, Kesim DK, Akçaalan Ö, Yavaş S, et al. Journal article Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice (2016) Gansevoort RT, Arici M, Benzing T, Birn H, Capasso G, Covic A, Devuyst O, et al. Journal article Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expression (2016) Muhlebner A, Iyer AM, Van Scheppingen J, Anink JJ, Jansen FE, Veersema TJ, Braun KP, et al. Journal article Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification (2016) Blümcke I, Aronica E, Becker A, Capper D, Coras R, Honavar M, Jacques TS, et al. Journal article Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes (2015) Bramswig NC, Luedecke HJ, Alanay Y, Albrecht B, Barthelmie A, Boduroglu K, Braunholz D, et al. Journal article