Search Results - "Alkan, Ö"

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    Assessment of Dietary Habits in Patients With Chronic Heart Failure by UYSAL, Hilal, ÖZ ALKAN, Havva, ENÇ, Nuray, YIĞIT, Zerrin

    Published in The Journal of Nursing Research (01-02-2020)
    “…Background: Nutritional deficiency is a critical factor in the development and prognosis of heart failure. An optimal diet should be ensured and maintained to…”
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    Journal Article
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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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    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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    Monitoring aseismic creep trends in the İsmetpaşa and Destek segments throughout the North Anatolian Fault (NAF) with a large-scale GPS network by Yavaşoğlu, Hasan Hakan, Alkan, Mehmet Nurullah, Bilgi, Serdar, Alkan, Öykü

    “…The North Anatolian Fault Zone (NAFZ) is an intersection area between the Anatolian and Eurasian plates. The Arabian Plate, which squeezes the Anatolian Plate…”
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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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