Hacettepe University

University / College


Location: Ankara, Turkey (TR) TR

ISNI: 0000000123427339

ROR: https://ror.org/04kwvgz42

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype-phenotype analysis (2019) Blümcke I, Coras R, Wefers AK, Capper D, Aronica E, Becker A, Honavar M, et al. Journal article, Review article Effect of peer delivered social stories on the crossing skills of primary school students with developmental disabilities (2019) Bıçakçı M, Gül SO Journal article Validation of Risk Scoring Systems in Ursodeoxycholic Acid-Treated Patients With Primary Biliary Cholangitis. (2019) Efe C, Tascilar K, Henriksson I, Lytvyak E, Alalkim F, Trivedi H, Eren F, et al. Journal article Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course (2019) Wefers AK, Stichel D, Schrimpf D, Coras R, Pages M, Tauziède-Espariat A, Varlet P, et al. Journal article Creativity in Research with Gifted Samples in Turkey (2018) Bicakci M, Baloglu M Journal article Fluoroquinolone prophylaxis in haematological cancer patients with neutropenia: ECIL critical appraisal of previous guidelines (2018) Mikulska M, Averbuch D, Tissot F, Cordonnier C, Akova M, Calandra T, Ceppi M, et al. Journal article MicroRNA519d and microRNA4758 can identify gangliogliomas from dysembryoplastic neuroepithelial tumours and astrocytomas. (2018) Bongaarts A, Prabowo AS, Arena A, Anink JJ, Reinten RJ, Jansen FE, Spliet WG, et al. Journal article 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