Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies von Paketci, C., Karakaya, M., Edem, P., Bayram, E., Keller, N., Daimagüler, H.-S., Cirak, S., Jordanova, A., Hiz, S., Wirth, B., Yiş, U.

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Clinical, radiological, and genetic survey of patients with muscle–eye–brain disease caused by mutations in POMGNT1 von Yiş, U, Uyanık, G, Rosendahl, D, Çarman, K, Bayram, E, Heise, M, Cömertpay, G, Kurul, S

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OP86 – 2425: Expression patterns of micro-RNAs 146a, 181a, and 155 in subacute sclerosing panencephalitis von Yiş, U, Tüfekçi, U.K, Gençsel, Ç, Çarman, K. Bora, Bayram, E, Topçu, Y, Kurul, S. Hiz

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PP07.3 – 3027: Simvastatin alleviates cell death and apoptosis in the developing brain of rat after pentylenetetrazole induced status epilepticus von Topçu, Y, Bayram, E, Ozbal, S, Yiş, U, Tugyan, K, Karaoglu, P, Yilmaz, O, Hiz, S

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Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG von Paketci, C., Edem, P., Hiz, S., Sonmezler, E., Soydemir, D., Sarikaya Uzan, G., Oktay, Y., O'Heir, E., Beltran, S., Laurie, S., Töpf, A., Lochmuller, H., Horvath, R., Yis, U.

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P077 Dentatorubral pallidoluysian atrophy in a Turkish family von Yiş, U, Dirik, E, Eken, A. Gündoğdu, Başak, N

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P248 Acute cerebellitis with cerebellar swelling successfully treated with standard dexamethasone treatment von Yiş, U, Kurul, S. Hız, Çakmakçı, H, Dirik, E

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P118 Effects of epilepsy and valproic acid on oxidant status in children with idiopathic epilepsy von Yiş, U, Seçkin, E, Kurul, S. Hız, Kuralay, F, Dirik, E

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P282 Clinical, pathological and radiological survey of patients with Leigh syndrome von Yiş, U, Kurul, S. Hız, Dirik, E, Çakmakçı, H, Özer, E

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P079 Myopathic electromyography, Diazepam responsive apneic attacks and congenital myasthenic syndrome von Yiş, U, Kurul, S. Hız, Öztura, I, Özden, Ö, Akıncı, G, Dirik, E

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P121 Erythrocyte lipid peroxidation and antioxidant enzyme levels in patients with febrile convulsion von Güneş, S, Dirik, E, Yiş, U, Seçkin, E, Kuralay, F, Köse, S, Ünalp, A

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NMP032 Congenital myotonic dystrophy: significance of family examination von Dirik, E, Yiş, U, Eren, S

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IAP029 Mycoplasma pneumonia: five different nervous system complications von Dirik, E, Yiş, U, Kurul, S, Çakmakçl, H

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MDP012 Cetirizine-induced acute dystonic reaction in a child von Esen, I, Demirpençe, S, Yiş, U, Kurul, S

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P119 Evaluation of serum lipids and carotid artery intima media thickness in epileptic children treated with valproic acid von Erdemir, A, Çullu, N, Yiş, U, Demircioğlu, F, Kır, M, Çakmakçı, H, Ünal, N, Dirik, E

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P283 Unusual findings in Leigh syndrome caused by T8993C mutation von Yiş, U, Seneca, S, Dirik, E, Kurul, S. Hız, Özer, E, Çakmakçı, H, De Meirleir, L

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P279 Two cases with megalencephalic leukoencephalopathy with subcortical cysts and MLC1 mutations in Turkish population von Yiş, U, Scheper, G.C, Uran, N, Ünalp, A, Çakmakçı, H, Kurul, S. Hız, Dirik, E, van der Knaap, M.S

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NMP030 Differential diagnosis of muscular hypotonia in infants: the kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VI) von Yiş, U, Dirik, E, Chambaz, C, Steinmann, B, Guinta, C

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MLP06 Multiple sulfatase deficiency: a report of two new cases resulting from a novel mutation von Yiş, U, Pepe, S, Ballabio, A, Cosma, M.P, Dirik, E

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NMO01 Different presentations of congenital muscular dystrophies von Yiş, U, Dirik, E, Kurul, S, Özer, E, Çakmakçl, H

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