Person: MATUR, ZELİHA
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Publication Metadata only Somatosensory Evoked Potentials In Patients With Juvenile Myoclonic Epilepsy(2016-01-01T00:00:00Z) Ozemir, Zeynep Aydin; Matur, ZELİHA; BAYKAL, Betül; ÖGE, Ali Emre; MATUR, ZELİHAWhile a small number of studies dealing with somatosensory evoked potential (SEP) have demonstrated hyperexcitability in the primary somatosensory cortex of juve-nile myoclonic epilepsy (JME) patients, the underlying mechanisms have yet to be illuminated. Determination of higher cortical SEP responses in some JME patients and recordings of very high amplitude responses, called -giant SEP,- in a specific subgroup may indicate a clinical and possibly genetic heterogeneity within JME patients. In the present review, the findings of previous studies concerned with SEP in JME patients are summarized, and their importance regarding JME etiopathogenesis and related clinical findings is discussed.Publication Metadata only Clinical Features of the -Optineurin- Mutation in familial FTD and ALS(2012-01-01T00:00:00Z) Cikrikcili, Ugur; Durmus, Hacer; Basak, Nazli; Gunel, Murat; GÜRVİT, İbrahim Hakan; Matur, ZELİHA; Akca Kalem, Sukriy; Serdaroglu-Oflazer, Piraye; Deymeer, Feza; Parman, Yesim; MATUR, ZELİHAPublication Metadata only Clinical, Electrophysiological, and Serological Evaluation of Patients with Cramp-Fasciculation Syndrome(2017-06-01T00:00:00Z) Poyraz, Muruvvet; Matur, ZELİHA; Aysal, Fikret; TÜZÜN, Erdem; Hanoglu, Lutfu; ÖGE, Ali Emre; MATUR, ZELİHAIntroduction: Cramp-fasciculation syndrome (CFS) is a rare peripheral nerve hyperexcitability syndrome. There are only a few reports on clinical and serological profile of a CFS cohort that was followed up by a single outpatient clinic.Publication Metadata only Evaluation of OnabotulinumtoxinA Treatment in Patients with Concomitant Chronic Migraine and Temporomandibular Disorders(2018-12-01T00:00:00Z) Kocaman, Gulsen; Kahraman, Nese; Gurkan Koseoglu, Banu; Bilgic, Basar; Ertas, Mustafa; Gulsen, Yesim; Baykan Baykal, Betul; MATUR, ZELİHAIntroduction: Migraine and temporomandibular disorders (TMD) are both common diseases and TMD are reported as a risk factor in migraine progression. OnabotulinumtoxinA is used in the treatment of chronic migraine (CM), and also has a potential role in TMD treatment. In this study, it is aimed to compare the efficacy of onabotulinumtoxinA treatment in CM patients with and without TMD.Publication Metadata only Effects of amantadine on postural instability in Parkinson-s disease(2014-05-01T00:00:00Z) Topcular, B.; Altinkaya, A.; Yabalak, A.; Kaymaz, A.; Altunrende, B.; Matur, ZELİHA; Gungor, O.; Altindag, E.; Demir, G. Akman; MATUR, ZELİHAPublication Metadata only Increased photosensitivity following short sleep in sleep deprived patients(2017-06-01T00:00:00Z) Elmali, Ayse Deniz; Kurucu, Hatice; Cetin, Ozdem Erturk; Cokar, Ozlem; Matur, ZELİHA; Dervent, Aysin; BENBİR ŞENEL, GÜLÇİN; Gurses, Candan; Demirbilek, Veysi; MATUR, ZELİHAIntroduction. We aimed to determine the effect of short day-time sleep on photoparoxysmal epileptic activity in sleep-deprived patients.Publication Metadata only Assosciation of autoimmune encephalitis with immune checkpoint inhibitor(2017-10-01T00:00:00Z) Altunrende, B.; Nalbantoglu, M.; Tuncer, O. Gungor; Matur, ZELİHA; Topcular, B.; Demir, G. Akman; MATUR, ZELİHAPublication Metadata only Genotypic and phenotypic presentation of TTR-FAP in Turkey(2014-05-01T00:00:00Z) DURMUŞ TEKÇE, Hacer; Matur, ZELİHA; Atmaca, M. M.; PODA, Mehveş; Oflazer-Serdaroglu, P.; Deymeer, F.; Parman, Y.; MATUR, ZELİHAPublication Metadata only Electromyography in Pediatric Population(2018-03-01T00:00:00Z) KOCASOY ORHAN, Elif; Baysal Kirac, Leyla; YALİNAY DİKMEN, PİNAR; Matur, ZELİHA; Ertas, Mustafa; ÖGE, Ali Emre; Deymeer, Feza; Yazici, Jale; BASLO, Mehmet Barış; MATUR, ZELİHAIntroduction: Electrodiagnostic evaluation provides an important extension to the neurological examination for the evaluation of pediatric neuromuscular disease. Many pediatric neuromuscular diseases are analogous to those seen in the adult. However, the relative frequency of these illnesses varies greatly when different age populations are compared. The purpose of the present study is to provide a retrospective analysis of children referred to our electromyography (EMG) laboratory for electrophysiological examinations.Publication Metadata only Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D(2014-05-01T00:00:00Z) Okamoto, Yuji; Goksungur, Meryem Tuba; Pehlivan, Davut; Beck, Christine R.; Gonzaga-Jauregui, Claudia; Muzny, Donna M.; Atik, Mehmed M.; Carvalho, Claudia M. B.; Matur, ZELİHA; BAYRAKTAR, Şerife; Boone, Philip M.; Akyuz, Kaya; Gibbs, Richard A.; Battaloglu, Esra; Parman, Yesim; Lupski, James R.; MATUR, ZELİHAPurpose: Copy-number variations as a mutational mechanism contribute significantly to human disease. Approximately one-half of the patients with Charcot-Marie-Tooth (CMT) disease have a 1.4Mb duplication copy-number variation as the cause of their neuropathy. However, non-CMTIA neuropathy patients rarely have causative copy-number variations, and to date, autosomal-recessive CMT disease has not been associated with copy-number Variation as a mutational mechanism.