T
Tulay Kansu
Researcher at Hacettepe University
Publications - 112
Citations - 3134
Tulay Kansu is an academic researcher from Hacettepe University. The author has contributed to research in topics: Optic neuropathy & Papilledema. The author has an hindex of 21, co-authored 112 publications receiving 2955 citations.
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Journal Article
Vascular involvement in Behçet's disease.
Yener Koc,Ibrahim Gullu,G Akpek,T Akpolat,Emin Kansu,S Kiraz,Figen Batman,Tulay Kansu,F Balkanci,S Akkaya +9 more
TL;DR: Patients with subcutaneous thrombophlebitis were more likely to develop major venous occlusions in the lower extremities and inferior vena cava and Arterial lesions were less frequent features constituting 12.0% of vascular complications in BD.
Journal ArticleDOI
Visual Loss in Pseudotumor Cerebri: Follow-up of 57 Patients From Five to 41 Years and a Profile of 14 Patients With Permanent Severe Visual Loss
James J. Corbett,Peter J. Savino,H S Thompson,Tulay Kansu,Norman J. Schatz,Linda S. Orr,D Hopson +6 more
TL;DR: It is believed that sequential quantitative perimetry gives more complete information and is essential to rational decision making in the treatment of pseudotumor cerebri.
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Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis
Joanna C. Jen,Wai-Man Chan,Thomas M. Bosley,Jijun Wan,Janai R. Carr,Udo Rüb,David W. Shattuck,G. Salamon,Lili C. Kudo,Jing Ou,Doris D. M. Lin,Mustafa A. Salih,Tulay Kansu,Hesham al Dhalaan,Zayed Al Zayed,David B. MacDonald,Bent Stigsby,Andreas Plaitakis,Emmanuel K. Dretakis,Irene Gottlob,Christina Pieh,Elias I. Traboulsi,Qing Kenneth Wang,Lejin Wang,Lejin Wang,Caroline Andrews,Koki Yamada,Joseph L. Demer,Shaheen Karim,Jeffry R. Alger,Daniel H. Geschwind,Thomas Deller,Nancy L. Sicotte,Stanley F. Nelson,Robert W. Baloh,Elizabeth C. Engle +35 more
TL;DR: In patients affected with HGPPS, mutations in the ROBO3 gene are identified, which shares homology with roundabout genes important in axon guidance in developing Drosophila, zebrafish, and mouse, and is required for hindbrain axon midline crossing.
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Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
Hilal Unal Gulsuner,Hilal Unal Gulsuner,Suleyman Gulsuner,Fatma Nazli Mercan,Onur Emre Onat,Tom Walsh,Hashem Shahin,Ming K. Lee,Okan Dogu,Tulay Kansu,Haluk Topaloglu,Bulent Elibol,Cenk Akbostanci,Mary Claire King,Tayfun Ozcelik,Tayfun Ozcelik,Ayse B. Tekinay +16 more
TL;DR: In a six-generation family with both essential tremor and Parkinson disease, a rare missense mutation of HTRA2 is identified as the causative allele, suggesting that in some families, HTRA 2 p.G399S is responsible for hereditary essential treMor and that homozygotes for this allele develop Parkinson disease.
Journal ArticleDOI
Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3
Thomas M. Bosley,M. A. Mohamed Salih,Joanna C. Jen,Doris D. M. Lin,D. Oystreck,Khaled K. Abu-Amero,David B. MacDonald,Z. Al Zayed,H. al Dhalaan,Tulay Kansu,Bent Stigsby,Robert W. Baloh +11 more
TL;DR: The major clinical characteristics of horizontal gaze palsy and progressive scoliosis were congenital horizontal gaze gazing and progressiveScoliosis with some variability in both ocular motility and degree of scoliotics.