Zobrazeno 1 - 10
of 47
pro vyhledávání: '"A. Emre Öge"'
Publikováno v:
Archives of Epilepsy, Vol 23, Iss 2, Pp 63-71 (2017)
Objectives:Rett syndrome (RS) is a neurodevelopmental disorder that primarily affects girls and is characterized by microcephaly, regression of language, loss of effective hand use, epilepsy, and electroencephalogram (EEG) abnormalities. This study i
Externí odkaz:
https://doaj.org/article/ebca5520fc984bccbc32acbe8e1360c4
Autor:
Burcu Ormeci, Handan Uzunçakmak Uyanık, Neslihan Taşdelen, Elif Çiğdem Keleş, Tibet Erdoğru, Ali Emre Öge
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 39, Iss 3, Pp 119-125 (2022)
Aim: Pudendal neuropathy (PN) is a common cause of chronic perineal pain and usually diagnosed long after the onset of symptoms. Diagnostic work-up of PN mainly includes radiologic and neurophysiological studies. However, there is no established diag
Externí odkaz:
https://doaj.org/article/c255e64a94034808832fc97573974422
Autor:
Zeliha Matur, A. Emre Öge, Hakan Gurvit, Cigdem Ulasoglu-Yildiz, Tamer Demiralp, Kardelen Eryurek
Publikováno v:
Cortex. 146:89-105
Motor sequence learning (MSL) paradigms are often used to investigate the neural processes underlying the acquisition of complex motor skills. Behavioral and neuroimaging studies have indicated an early stage in which spatial learning is prominent an
Autor:
Hatice Tankisi, Pieter A. van Doorn, Robert D. Henderson, Leonard H. van den Berg, Ruben P A van Eijk, Boudewijn T.H.M. Sleutjes, A. Emre Öge, A.B. Jacobsen, N. Gorkem Sirin
Publikováno v:
Sleutjes, B T H M, Bystrup Jacobsen, A, Tankisi, H, Gorkem Sirin, N, Emre Oge, A, Henderson, R D, van Doorn, P A, van den Berg, L H & van Eijk, R P A 2021, ' Advancing disease monitoring of amyotrophic lateral sclerosis with the compound muscle action potential scan ', Clinical Neurophysiology, vol. 132, no. 12, pp. 3152-3159 . https://doi.org/10.1016/j.clinph.2021.09.014
Clinical Neurophysiology, 132(12), 3152-3159. Elsevier Ireland Ltd
Clinical Neurophysiology, 132(12), 3152-3159. Elsevier Ireland Ltd
Objective To determine which compound muscle action potential (CMAP) scan-derived electrophysiological markers are most sensitive for monitoring disease progression in amyotrophic lateral sclerosis (ALS), and whether they hold value for clinical tria
Publikováno v:
Biomedical Signal Processing and Control. 51:264-276
Artuğ, Necdet Tuğrul (Arel Author)
The present study aims to develop an algorithm and software that automatically detects repeater F-waves which are very difficult to analyze when elicited as high number of recordings in motor unit number esti
The present study aims to develop an algorithm and software that automatically detects repeater F-waves which are very difficult to analyze when elicited as high number of recordings in motor unit number esti
Publikováno v:
The Journal of Prosthetic Dentistry. 120:173-176
Oromandibular dystonia (OMD) is defined as a subset of movement disorders characterized by involuntary muscle contraction in different parts of the oromandibular region. This clinical report presents a multidisciplinary approach to the management of
Autor:
Lale Mehdikhanova, A. Emre Öge, Pınar Bekdik Şirinocak, Tuba Akıncı, Nuran Burcu Arkali, M. Baris Baslo, Fatma Candan, Tuba Cerrahoğlu Şirin, Elif Kocasoy Orhan
Publikováno v:
Turkiye Klinikleri Journal of Neurology. 13:1-6
Akademický článek
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Autor:
Halil Atilla Idrisoglu, Tugrul Artug, Bahar Erbas, N. Gorkem Sirin, Emel Oguz Akarsu, A. Emre Öge, M. Baris Baslo, Elif Kocasoy Orhan, H Ozlem Dede
WOS: 000479282600001
PubMed ID: 31330055
Artuğ, Tuğrul (Arel Author)
Introduction The objective of this study was to determine compound muscle action potential (CMAP) scan parameters and MScanFit motor unit number estimation (MUNE) i
PubMed ID: 31330055
Artuğ, Tuğrul (Arel Author)
Introduction The objective of this study was to determine compound muscle action potential (CMAP) scan parameters and MScanFit motor unit number estimation (MUNE) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dabb8dfa0b73cceefda5edc85238e31
https://hdl.handle.net/20.500.12294/1677
https://hdl.handle.net/20.500.12294/1677
Publikováno v:
Epilepsy & Behavior. 112:107479
Objective The objective of the study was to investigate the effects of slow repetitive transcranial magnetic stimulation (rTMS) on patients with refractory juvenile myoclonic epilepsy (JME). Methods One thousand pulses with the intensity of 120% acti