Search Results - "Oğuz, K.K."

Increased Gray Matter Density in the Parietal Cortex of Mathematicians: A Voxel-Based Morphometry Study by Aydin, K, Ucar, A, Oguz, K.K, Okur, O.O, Agayev, A, Unal, Z, Yilmaz, S, Ozturk, C

“…The training to acquire or practicing to perform a skill, which may lead to structural changes in the brain, is called experience-dependent structural…”
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ETO02 Outcome after resective surgery for epilepsy in children by Turanli, G, Yalnizoğlu, D, Açikgöz, D, Saatçi, I, Oğuz, K.K, Söylemezoğlu, F, Erbaş, B, Ergün, E.L, Akalan, N, Topçu, M

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Ornithine transcarbamylase deficiency presenting with acute reversible metabolic stroke in a child by Dedeoglu, O, Kasapkara, C, Oguz, K.K, Altınel, E, Häberle, J, Aksoy, A

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A case with acute reversible bilateral ptosis: SURF-1 deficiency by Dedeoglu, O, Yüksel, D, Sel Ç, Genc, Aksoy, E, Kilic, M, Oguz, K.K, Talim, B

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P83 – 2742: Clinical characteristics of MLD patients admitted to Hacettepe University in one-year period by Topçu, M, Günbey, C, Ardiçli, D, Oguz, K.K

“…Objective Metachromatic leukodystrophy (MLD) is a rare lysosomal storage disorder caused by deficieny of arylsulfatase A (ARSA), leading to accumulation of…”
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Complete Labyrinthine Aplasia: Clinical and Radiologic Findings with Review of the Literature by Ozgen, B, Oguz, K.K, Atas, A, Sennaroglu, L

“…Complete labyrinthine aplasia (CLA), also referred to as Michel aplasia, is a severe congenital anomaly of the inner ear, defined by the complete absence of…”
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INV5 Radiological differential diagnosis of inflammatory disorders by Oguz, K.K

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P-796 - Assessment of alteration in white matter integrity in schizophrenia following administration of clozapine: tract-based spatial statistics of diffusion tensor imaging by Ozcelik Eroglu, E, Ertugrul, A, Oguz, K.K, Has, A.C, Yazici, M.K

“…Introduction Several diffusion tensor imaging (DTI) studies have shown disturbed white matter integrity in various brain areas in schizophrenia patients…”
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Cerebral Alveolar Echinoccosis Mimicking Primary Brain Tumor by Senturk, S, Oguz, K.K, Soylemezoglu, F, Inci, S

“…We present a case of cerebral infestation by Echinococcosis multilocularis mimicking an infiltrative primary brain tumor. A heavily calcified mass invading the…”
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Epidermal Nevus Syndrome with Internal Carotid Artery Occlusion and Intracranial and Orbital Lipomas by Canyigit, M, Oguz, K.K

“…We report a case of epidermal nevus syndrome involving the brain in which there is chronic occlusion of the left distal internal carotid artery resulting in…”
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PO18-WE-52 Postoperative prognosis in adult epilepsy patients after functional hemispherotomy or hemispherectomy by Dericioglu, N, Tezer, F.I, Oguz, K.K, Soylemezoglu, F, Ciger, A, Akalan, N, Saygi, S

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Assessment of Citrullinated Myelin by 1H-MR Spectroscopy in Early-Onset Multiple Sclerosis by Oguz, K.K, Kurne, A, Aksu, A.O, Karabulut, E, Serdaroglu, A, Teber, S, Haspolat, S, Senbil, N, Kurul, S, Anlar, B

“…Myelin instability and citrullinated myelin basic protein have been demonstrated in the brains of patients with chronic and fulminating forms of multiple…”
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IAP043 Limbic encephalitis in a 9-year-old child due to voltage-gated potassium channel antibody (VGKC-Ab) by Cakmakli, H.F, Oguz, K.K, Haliloglu, G, Topcu, M

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Neurochemical evaluation of brain function with 1 H magnetic resonance spectroscopy in patients with fragile X syndrome by Utine, G.E., Akpınar, B., Arslan, U., Kiper, P.Ö.Ş., Volkan‐Salancı, B., Alanay, Y., Aktaş, D., Haliloğlu, G., Oğuz, K.K., Boduroğlu, K., Alikaşifoğlu, M.

“…ABSTRACT Fragile X syndrome (FXS) is the most common hereditary disorder of intellectual disability. Cognitive deficits involve executive function, attention,…”
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IAP035 Recurrent pseudotumoural hemicerebellitis: case report of a patient with review of the literature by Haliloglu, G, Oguz, K.K, Bircan, O, Alehan, D, Topcu, M

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Brachial Plexus Ultrasound and MRI in Children with Brachial Plexus Birth Injury by Gunes, A, Bulut, E, Uzumcugil, A, Oguz, K K

“…Brachial plexus birth injury is caused by traction on the neck during delivery and results in flaccid palsy of an upper extremity commonly involving C5-C6…”
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Neurochemical evaluation of brain function with 1H magnetic resonance spectroscopy in patients with fragile X syndrome by Utine, G.E., Akpınar, B., Arslan, U., Kiper, P.Ö.Ş., Volkan-Salancı, B., Alanay, Y., Aktaş, D., Haliloğlu, G., Oğuz, K.K., Boduroğlu, K., Alikaşifoğlu, M.

“…ABSTRACT Fragile X syndrome (FXS) is the most common hereditary disorder of intellectual disability. Cognitive deficits involve executive function, attention,…”
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IAP026 Central nervous system involvement in paediatric SLE: Do we need an MRI? by Demirkaya, E, Bilginer, Y, Yalnizoglu, D, Oguz, K.K, Isikhan, V, Besbas, N, Bakkaloglu, A, Ozen, S

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MLP03 Peripheral neuropathy as an additional feature in D-2-hydroxyglutaric aciduria by Haliloglu, G, Temucin, C, Oguz, K.K, Celiker, A, Coskun, T, Sass, O, Fischer, J, Topcu, M

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MLP04 Is there a link betweeen L-2-hydroxyglutaric aciduria and brain tumors? – report of two patients with medulloblastoma and glioblastoma multiforme by Haliloglu, G, Celik, I, Oguz, K.K, Anlar, B, Ozisik, P, Akalan, N, Soylemezoglu, F, Coskun, T, Sass, O, Fischer, J, Topcu, M

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