Search Results - "İncecik,Faruk"

Evaluation of the relationship between NIRS (near-infrared spectroscopy) and optic nerve sheath diameter measurement in children with increased intracranial pressure: a pilot study by Arslan, Didar, Yıldızdaş, Dinçer, Horoz, Özden Özgür, Aslan, Nagehan, İncecik, Faruk

“…The increased intracranial pressure (ICP) syndrome may emerge depending on many different neurological factors and the early diagnosis and treatment are…”
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Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome by Roosing, Susanne, Hofree, Matan, Kim, Sehyun, Scott, Eric, Copeland, Brett, Romani, Marta, Silhavy, Jennifer L, Rosti, Rasim O, Schroth, Jana, Mazza, Tommaso, Miccinilli, Elide, Zaki, Maha S, Swoboda, Kathryn J, Milisa-Drautz, Joanne, Dobyns, William B, Mikati, Mohamed A, İncecik, Faruk, Azam, Matloob, Borgatti, Renato, Romaniello, Romina, Boustany, Rose-Mary, Clericuzio, Carol L, D'Arrigo, Stefano, Strømme, Petter, Boltshauser, Eugen, Stanzial, Franco, Mirabelli-Badenier, Marisol, Moroni, Isabella, Bertini, Enrico, Emma, Francesco, Steinlin, Maja, Hildebrandt, Friedhelm, Johnson, Colin A, Freilinger, Michael, Vaux, Keith K, Gabriel, Stacey B, Aza-Blanc, Pedro, Heynen-Genel, Susanne, Ideker, Trey, Dynlacht, Brian D, Lee, Ji Eun, Valente, Enza Maria, Kim, Joon, Gleeson, Joseph G

“…Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies, including Joubert syndrome (JS), with defective cerebellar vermis…”
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Peripheral facial nerve palsy in children: clinical manifestations, treatment and prognosis by Bilge, Serap, Mert, Gülen Gül, Hergüner, M Özlem, İncecik, Faruk, Sürmelioğlu, Özgür, Bilen, Sevcan, Yılmaz, Levent

“…Sudden onset of unilateral weakness of the upper and lower muscles of one side of the face is defined as peripheral facial nerve palsy. Peripheral facial nerve…”
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Coexistence of two rare genetic disorders: Cystic fibrosis and megalencephalic leukoencephalopathy with subcortical cysts in a child by İncecik,Faruk, Yılmaz,Mustafa, Bişgin,Atıl

“…Cystic fibrosis (CF) is the most common autosomal recessive disease with fatal outcome in Caucasians with a frequency of 1 in 2500 live births. It is caused by…”
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Neurological complications of pandemic influenza (H1N1) in children by Yıldızdaş, Dinçer, Kendirli, Tanıl, Arslanköylü, Ali Ertuğ, Horoz, Özden Özgür, İncecik, Faruk, İnce, Erdal, Çiftçi, Ergin

“…The aim of this study was to determine the clinical characteristics of children demonstrating neurological complications with pandemic influenza (H1N1). We…”
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Potassium Bromide for Treatment of Malignant Migrating Partial Seizures in Infancy by Uenver, Olcay, Incecik, Faruk, Duendar, Huelya, Komuer, Mustafa, Uenver, Afsin, Okuyaz, Cetin

“…Abstract Background The syndrome of malignant migrating partial seizures in infancy is a rare epileptic syndrome with a devastating course characterized by…”
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Neurofibromatosis type 1 and cardiac manifestations by Incecik, Faruk

“…Cardiac manifestations of neurofibromatosis type 1 (NF1) may include hypertension, congenital heart disease, and hypertrophic cardiomyopathy. The aim of this…”
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Telomerase activity in patients with neurofibromatosis Type-1 by Küpeli,Serhan, Altunbaşak,Şakir, İncecik,Faruk, Arkan,Ayçin

“…Purpose: In various studies low telomerase activity have been shown to have a protective role in some types of cancer. Patients with neurofibromatosis type-1…”
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Pseudotumor cerebri in children: Etiology, clinical findings, prognosis by Mert,Gülen Gül, Özcan,Neslihan, Beşen,Şeyda, Yar,Kemal, Hergüner,Mihriban Özlem, İncecik,Faruk, Altunbaşak,Şakir

“…Purpose: Clinical and neuroimaging findings, aetiologies, treatment modalities and durations, response to treatment, and neurological sequelae of the patients…”
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Evaluation of 17 Patients With Transverse Myelitis in Terms of Clinical, Treatment and Prognosis by Murat Turhan, Faruk İncecik, Mihriban Özlem Hergün, Dinçer Yıldızdaş, Sakir Altunbaşak

“…INTRODUCTION: In this study, it was aimed to identify the clinical findings, treatment modalities and factors affecting the prognosis of patients who were…”
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Akut Karın ile Gelen Guillain-Barre Sendromu by İncecik, Faruk, Horoz, Özden Özgür, Hergüner, M. Özlem, Yıldızdaş, Dinçer

“…Guillain-Barre Sendromu (GBS), çocukluk çağındaki akut flask paralizinin en sık nedenidir. Simetrik güçsüzlük, baş ağrısı, solunum sıkıntısı, nöropatik ağrı,…”
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Idiopathic Childhood Occipital Lobe Epilepsies In Turkish Children by Altunbaşak,Şakir, Mert,Gülen, Hergüner,Mihriban Özlem, İncecik,Faruk

“…Purpose: Two forms of idiopathic occipital lobe epilepsy can be distinguished: an early onset or Panayiotopoulos type (PS), and a late onset or Gastaut type…”
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Tekrarlayan Fasiyal Paralizili bir olgu: Melkersson-Rosenthal Sendromu by Bulut, Derya Fatma, Mert, Gülen Gül, İncecik, Faruk, Hergüner, Özlem Mihriban, Altunbaşak, Şakir

“…Melkersson-Rosenthal sendromu (MRS), tekrarlayan fasiyal paralizi, orofasiyal ödem, dilde fissürle karakterize nadir bir nöromukokütanöz sendromdur…”
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L-2-Hidroksi Glutarik Asidüri: Üç Olgu Sunumu by İncecik, Faruk, Mungan, Neslihan, Hergüner, Özlem Mihriban, Kör, Deniz, Şeker, Berna, Altunbasak, Sakir

“…L-2-hidroksiglutarik asidüri nadir rastlanan, otozomal resesif geçişli, metabolik bir hastalıktır. Hastalık zihinsel engellilik, ataksi, ekstrapiramidal…”
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Hereditary Spastic Paraplegia Type 26 with a Novel Mutation in B4GALNT1 Gene and Literature Review of the Clinical Features by Incecık, Faruk, Herguner, Ozlem M, Bozdogan, Sevcan Tug

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Çocuklarda psödotümör serebri: etyoloji, klinik bulgular, prognoz by Gülen GÜL MERT, Neslihan ÖZCAN, Şeyda BEŞEN, Kemal YAR, Özlem HERGÜNER, Faruk İNCECİK, Şakir ALTUNBAŞAK

“…Amaç: Psödotümör serebri tanısı alan hastaların klinik ve nörogörüntüleme bulguları, etiyolojileri, tedavi şekilleri ve süreleri, tedaviye yanıtları ve…”
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Cyclosporin Treatment in Three Children With Chronic Inflammatory Demyelinating Neuropathy by OZLEM HERGÜNER, M, INCECIK, Faruk, ALTUNBASAK, Sakir

“…Chronic inflammatory demyelinating neuropathy is an uncommon acquired polyneuropathy in children. Oral prednisolone, intravenous methyl prednisolone, and…”
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Epilepsy and McArdle Disease in a Child by İncecik, Faruk, Hergüner, Özlem, Mert, Gülen, Besen, Şeyda, Kor, Deniz, Yılmaz, Berna, Mungan, Neslihan Önenli, Altunbaşak, Şakir

“…McArdle hastalığı, çizgili kasta glikojen fosforilaz enziminin eksikliği sonucu gelişen, otozomal resesif kalitim gösteren bir hastalık olarak…”
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Clinical Characteristics of 10 Patients With Continuous Spikes and Waves During Slow Sleep Syndrome by HERGIINER, M. Ozlem, INCECIK, Faruk, ALTUNBASAK, Sakir, KIRIS, Nurcihan

“…Continuous spikes and waves during slow sleep syndrome is characterized by the presence of spike-and-wave discharges in at least 85% of non–rapid eye movement…”
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Homozygous Mutation in CWF19L1 with Recessive Ataxia Syndrome in a Turkish Child by Incecik, Faruk, Ozcanyuz, Duygu G, Bozdogan, Sevcan T, Herguner, Ozlem M

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