Search Results - "Yalcinkaya, C."

Flexural strengthening of RC beams using UHPFRC laminates: Bonding techniques and rebar addition by Tanarslan, H.M., Alver, N., Jahangiri, R., Yalçınkaya, Ç., Yazıcı, H.

“…•RC specimens strengthened with UHPFRC laminates were tested in the laboratory.•Two different bonding methods: gluing with epoxy and mechanical anchoring were…”
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A different technique for the closure of trocar sites by Yalcinkaya, C, Coban, G, Parlakgumus, A, Caglar, P, Cologlu, H, Ozdemir, H

“…This study aims to present a different technique for the closure of trocar sites in laparoscopic surgeries. Retrospective records of cases who received the new…”
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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease by Bilir, B, Yapici, Z, Yalcinkaya, C, Baris, I, Carvalho, CMB, Bartnik, M, Ozes, B, Eraksoy, M, Lupski, JR, Battaloglu, E

“…Bilir B, Yapici Z, Yalcinkaya C, Baris I, Carvalho CMB, Bartnik M, Ozes B, Eraksoy M, Lupski JR, Battaloglu E. High frequency of GJA12/GJC2 mutations in…”
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Seizures during treatment of Vitamin B12 deficiency by Benbir, G, Uysal, S, Saltik, S, Zeybek, C. Aktuglu, Aydin, A, Dervent, A, Yalcinkaya, C

“…Summary Epileptic seizures during infancy have a wide variety of clinical presentations and the outcome differs according to the etiology. Among the benign and…”
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Operative hysteroscopy preserving virginity: a new technique by Yalcinkaya, C, Kalayci, H, Simsek, E, Iskender, C T, Parlakgumus, H A

“…To present a new technique of virginity-preserving operative hysteroscopy in the treatment of intrauterine pathologies. The details of operative hysteroscopy…”
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Identification of seven novel mutations in the GAN gene by Bomont, P., Ioos, C., Yalcinkaya, C., Korinthenberg, R., Vallat, JM, Assami, S., Munnich, A., Chabrol, B., Kurlemann, G., Tazir, M., Koenig, M.

“…Giant axonal neuropathy (GAN) is a severe early onset neurodegenerative disorder affecting both the peripheral nerves and the central nervous system. The…”
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MRI findings in pediatric neuro-Behçet's disease by Saltik, S, Saip, S, Kocer, N, Siva, A, Yalçinkaya, C

“…Behçet's disease (BD), a systemic vasculitis of unknown cause, affects many organs and systems. Neurological involvement is seen in 5-15% of the patients, and…”
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Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency by Dervent, A, Gibson, K.M, Pearl, P.L, Salomons, G.S, Jakobs, C, Yalcinkaya, C

“…Succinic semialdehyde dehydrogenase (SSADH) deficiency is a neurometabolic disorder characterized by excessive GABA levels and seizures. There has been no…”
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Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children by Toelle, S P, Yalcinkaya, C, Kocer, N, Deonna, T, Overweg-Plandsoen, W C G, Bast, T, Kalmanchey, R, Barsi, P, Schneider, J F L, Capone Mori, A, Boltshauser, E

“…Rhombencephalosynapsis is a rare congenital abnormality characterised by dorsal fusion of the cerebellar hemispheres, agenesis or hypogenesis of the vermis,…”
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Atypical MRI findings in Canavan disease: a patient with a mild course by Yalcinkaya, C, Benbir, G, Salomons, G S, Karaarslan, E, Rolland, M O, Jakobs, C, van der Knaap, M S

“…Canavan disease is a severe, progressive leukodystrophy with an autosomal recessive inheritance, caused by aspartoacylase (ASPA) deficiency. The characteristic…”
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1.314 Clinical characteristics of 49 patients with psychogenic movement disorders in a tertiary clinic in Turkey by Ozekmekci, S, Ertan, S, Kiziltan, G, Uluduz, D, Ertan, T, Yalcinkaya, C, Ozkara, C

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Two new cases with progressive cavitating leukoencephalopathy by Yapici, Z, Benbir, G, Saltik, S, Ertugrul, B, Naidu, S, Yalcinkaya, C

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Two cases with progressive cystic leukoencephalopathy by Yapici, Z, Benbir, G, Saltik, S, He, L, Brown, G K, Taylor, R W, Dincer, A, Naidu, S, Yalcinkaya, C

“…Leukoencephalopathies with cystic changes in the white matter on magnetic resonance imaging are aetiologically heterogeneous neurological disorders seen in…”
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MRI findings in succinic semialdehyde dehydrogenase deficiency by Yalçinkaya, C, Gibson, K M, Gündüz, E, Koçer, N, Fiçicioğlu, C, Küçükercan, I

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MRI and MRS in HMG-CoA lyase deficiency by YALCINKAYA, C, DINCER, A, GÜNDÜZ, E, FICICIOGLU, C, KOCER, N, AYDIN, A

“…3-Hydroxy-3-Methylglutaryl coenzyme A lyase (HMG-CoA) deficiency is a rare inborn error of leucine catabolism. The disease is characterized by recurrent…”
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Ictal and interictal SPECT findings in childhood absence epilepsy by Yeni, S.Naz, Kabasakal, Levent, Yalçinkaya, Cengiz, Nisli, Cavit, Dervent, Aysin

“…The purpose of this study was to investigate the informative value of single photon emission tomography (SPECT) in relation to the pathophysiological…”
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Neuroimaging findings of four patients with Sandhoff disease by Yüksel, Adnan, Yalçınkaya, Cengiz, Işlak, Civan, Gündüz, Erem, Seven, Mehmet

“…Sandhoff disease is a severe form of GM 2 gangliosidosis that is caused by the deficiency of both hexosaminidase A and B. Startle reaction, hypotonia,…”
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Progressive white-matter disease with primary cerebellar involvement: a separate entity? by YALCINKAYA, C, ARSLANOGLU, I, ISLAK, C, AYDIN, A, BOLTSHAUSER, E

“…Although its metabolic basis has not yet been clarified, we report a progressive white-matter disease in a Turkish girl, starting in the cerebellum and…”
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Delayed-onset dystonia associated with 3-oxothiolase deficiency by Yalçinkaya, Cengiz, Apaydin, Hülya, Özekmekçi, Sibel, Gibson, K. Michael

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Siblings With Cystic Leukoencephalopathy and Megalencephaly by Yalçinkaya, Cengiz, Çomu, Sinan, Koçer, Naci, Yüksel, Adnan, Gündüz, Erem, Demirbilek, Veysi, Ocal, Ayla

“…Cystic leukoencephalopathy with megalencephaly is a newly described entity with mild clinical involvement. Patients suffer from developmental problems and…”
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