Hacettepe University


Universität / Hochschule

Standort der Organisation:
Ankara, Türkei


Publikationen in Kooperation mit FAU-Wissenschaftern


Blümcke, I., Coras, R., Wefers, A.K., Capper, D., Aronica, E., Becker, A.,... Thom, M. (2019). Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis. Neuropathology and Applied Neurobiology, 45(2), 95-107. https://dx.doi.org/10.1111/nan.12522
Germeshausen, M., Ancliff, P., Estrada, J., Metzler, M., Ponstingl, E., Ruetschle, H.,... Ballmaier, M. (2018). MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia. Blood Advances, 2(6), 586-596. https://dx.doi.org/10.1182/bloodadvances.2018016501
Bongaarts, A., Giannikou, K., Reinten, R.J., Anink, J.J., Mills, J.D., Jansen, F.E.,... Aronica, E. (2017). Subependymal giant cell astrocytomas in Tuberous Sclerosis Complex have consistent TSC1/TSC2 biallelic inactivation, and no BRAF mutations. Oncotarget, 8(56), 95516-95529. https://dx.doi.org/10.18632/oncotarget.20764
Kerse, C., Kalaycıoğlu, H., Elahi, P., Çetin, B., Kesim, D.K., Akçaalan, Ö.,... Ilday, F. (2016). Ablation-cooled material removal with ultrafast bursts of pulses. Nature, 537(7618), 84-88. https://dx.doi.org/10.1038/nature18619
Blümcke, I., Aronica, E., Becker, A., Capper, D., Coras, R., Honavar, M.,... Thom, M. (2016). Low-grade epilepsy-associated neuroepithelial tumours - the 2016 WHO classification. Nature Reviews Neurology, 12(12), 732-740. https://dx.doi.org/10.1038/nrneurol.2016.173
Gansevoort, R.T., Arici, M., Benzing, T., Birn, H., Capasso, G., Covic, A.,... Van Biesen, W. (2016). 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. Nephrology Dialysis Transplantation, 31(3), 337-48. https://dx.doi.org/10.1093/ndt/gfv456
Muhlebner, A., Iyer, A.M., Van Scheppingen, J., Anink, J.J., Jansen, F.E., Veersema, T.J.,... Aronica, E. (2016). Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expression. Journal of Neurodevelopmental Disorders, 8, 9. https://dx.doi.org/10.1186/s11689-016-9142-0
Bramswig, N.C., Luedecke, H.-J., Alanay, Y., Albrecht, B., Barthelmie, A., Boduroglu, K.,... Wieczorek, D. (2015). Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes. Human genetics, 134(6), 553-68. https://dx.doi.org/10.1007/s00439-015-1535-8
Maass, P.G., Aydin, A., Luft, F.C., Schaechterle, C., Weise, A., Stricker, S.,... Baehring, S. (2015). PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics, 47(6), 647-53. https://dx.doi.org/10.1038/ng.3302

Zuletzt aktualisiert 2013-02-07 um 12:21