Search Results - "Alkan, O."

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    Submicron R2Fe14B particles by Koylu-Alkan, O., Barandiaran, J. M., Salazar, D., Hadjipanayis, G. C.

    Published in AIP advances (01-05-2016)
    “…Mechanochemical synthesis of submicron R2Fe14B particles with R = Dy, Nd, Pr has been performed successfully via high energy ball milling of rare-earth oxides,…”
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    Journal Article
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    P71 – 2336: Brain and spinal MR imaging findings in metachromatic leukodystrophy: Enhancing cranial nerves and cauda equina by Alkan, O, Erol, I, Saygi, S

    Published in European journal of paediatric neurology (01-05-2015)
    “…Objective To present contrast-enhanced brain and spinal MR imaging findings two patients with metachromatic leukodystrophy (MLD). Methods The patients…”
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    P57 – 2330: An infant with later onset Aicardi-Goutieres syndrome caused by homozygous TREX1 gene mutation by Erol, I, Misirlioglu, P.K, Savas, T, Alkan, O

    Published in European journal of paediatric neurology (01-05-2015)
    “…Objective Aicardi-Goutieres syndrome (AGS) is both genetically and phenotypically heterogeneous disorder. Mutations in five genes – TREX1, RNASEH2B, RNASEH2C,…”
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    P78 – 2554: Farber disease in a child with a novel homozygous c.92G>T mutation by Saygi, S, Haytoglu, Z, Savas, T, Alkan, O, Erol, I

    Published in European journal of paediatric neurology (01-05-2015)
    “…Objective Farber disease is an extremely rare autosomal recessive lysosomal storage disease marked by a deficiency in enzyme acid ceramidase that causes an…”
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    524 Two Pediatric Cases of Cerebral Venous Sinus Thrombosis with Different Presentations by Kiliçaslan, B, Erol, I˙, Yazıcı, N, Alkan, Ö

    Published in Archives of disease in childhood (01-10-2012)
    “…Background and Aims Cerebral Venous Sinus Thrombosis (CVST) is a serious and rare disorder in pediatric patients. Case reports: Case 1: An 8-year-old girl…”
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    546 A Giant Orbital Plexiform Neurofibroma with Massive Intracranial Extention in a Newborn by Yazici, N, Gulcan, H, Alkan, O, Yaycioglu, R, Bal, N, Sarialioglu, F

    Published in Archives of disease in childhood (01-10-2012)
    “…Orbital masses in newborns are rare. Herein a newborn with a giant orbital tumor is presented. A 10-day female baby was admitted to hospital with proptosis…”
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    Changes of tumor necrosis factor-α, interleukin-10, and tartrate-resistant acid phosphatase5b in the crevicular fluid in relation to orthodontic movement by Karaduman, B, Uraz, A, Altan, GN, Baloş Tuncer, B, Alkan, Ö, Gönen, S, Pehlivan, S, Çetiner, D

    Published in European journal of inflammation (01-04-2015)
    “…The aim of this study was to determine gingival crevicular fluid (GCF) expressions of tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10), and…”
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    Congenital infiltrating lipomatosis of the face with hemimegalencephaly by Alkan, O, Yildirim, T, Seyhan, T, Erbay, G, Erol, I

    Published in Neuropediatrics (01-06-2009)
    “…Congenital infiltrating lipomatosis of the face (CILF) is a rare disorder, causing unilateral facial asymmetry characterized by enlargement of the cheek or…”
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    Data-driven spatio-temporal RGBD feature encoding for action recognition in operating rooms by Twinanda, Andru P., Alkan, Emre O., Gangi, Afshin, de Mathelin, Michel, Padoy, Nicolas

    “…Purpose Context-aware systems for the operating room (OR) provide the possibility to significantly improve surgical workflow through various applications such…”
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    Paraparesis following straining accompanied by spontaneous thoracolumbar spinal epidural hematoma: a case report by Birol Sarica, F, Tufan, K, Cekinmez, M, Sen, O, Alkan, O, Caner, H

    Published in Journal of neurosurgical sciences (01-06-2009)
    “…Spontaneous spinal epidural hematoma (SSEH) is a rare disease that requires emergency surgical intervention because it can cause serious and permanent…”
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    Ventral Thoracic Spinal Cord Herniation: A Commonly Misdiagnosed and Treatable Cause of Myelopathy by Alkan, O., Kizilkilic, O., Goksel, B. Karakurum, Yildirim, T., Sarica, F. Birol

    Published in The neuroradiology journal (01-08-2008)
    “…Idiopathic ventral spinal cord herniation is a rare cause of progressive myelopathy that demonstrates unique radiological features. We describe a case of…”
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