Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Abidin Erdal"'
Autor:
Firdevs Ezgi Uçan Tokuç, Fatma Genç, Eylem Özaydın Göksu, Abidin Erdal, Yasemin Biçer Gömceli
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionFor epilepsy, a common neurological disorder, brings psychosocial challenges like stigma, employment difficulties, and barriers to marriage and childbearing. Stigma often stems from misconceptions and societal beliefs, particularly in les
Externí odkaz:
https://doaj.org/article/df0abe9b24b74141ab4a20fba881f6ab
Autor:
Arife Çimen Atalar, Aynur Özge, Bengi Gül Türk, Esme Ekizoğlu, Duygu Kurt Gök, Betül Baykan, Semih Ayta, Füsun Ferda Erdoğan, Seher Naz Yeni, Bahar Taşdelen, IDEM Study Group, Sibel K. Velioğlu, Zuhal Yapıcı, İpek Midi, Saygı Serap, Çelebi Ulufer, Elif Sarıca Darol, Kadriye Ağan, Senem Ayç, Sibel Gazioğlu, Zeynep Vildan Okudan, Nermin Görkem Şirin, Nerses Bebek, Neşe Dericioğlu, İlknur Güçlü Altun, Ayşe Destina Yalçın, Reyhan Sürmeli, Oğuz Osman Erdinç, Abidin Erdal, Demet İlhan Algın, Gülnihal Kutlu, Semai Bek, Yüksel Erdal, Akçay Övünç Özön, Aylin Reyhani, Babürhan Güldiken, Barış Baklan, Bülent Oğuz Genç, Ebru Aykutlu Altindağ, Gökçen Karahan, Güray Koç, Handan Mısırlı, İbrahim Öztura, Kezban Aslan-Kara, Melodi Çakar Merve, Nur Türkmen, Onur Bulut, Karadaş Ömer, Özlem Kesim Çahin, Sevgi Ferik, Taylan Peköz Mehmet, Pınar Topaloğlu, Sibel Üstün Özek, Ülkühan Düzgün, Vildan Yayla, Yasemin Gömceli, Zeynep Ünlüsoy Acar
Publikováno v:
Frontiers in Neurology, Vol 13 (2023)
BackgroundMigraine without aura (MwoA) is a very frequent and remarkable comorbidity in patients with idiopathic/genetic epilepsy (I/GE). Frequently in clinical practice, diagnosis of MwoA may be challenging despite the guidance of current diagnostic
Externí odkaz:
https://doaj.org/article/63f182df8f6b4bcdb757b52ed7bc79f9
Autor:
Eylem ÖZAYDIN GÖKSU, Abidin ERDAL
Publikováno v:
Archives of Epilepsy, Vol 26, Iss 1, Pp 20-24 (2020)
Objectives:Some hemogram parameters, which may be indicative of inflammation and hypoxemia, have been shown to be related to epilepsy and stroke disease in previous studies. The present study aims to investigate whether hemogram parameters are indica
Externí odkaz:
https://doaj.org/article/4882f5093263452888cce97832129fbc
Publikováno v:
Archives of Epilepsy, Vol 26, Iss 1, Pp 7-11 (2020)
Objectives:Antiepileptic drugs are the most commonly used treatments in epilepsy. However, in a group of about one-third of all epilepsy patients who have not been able to control seizures with antiepileptic drugs called drug-resistant epilepsy, epil
Externí odkaz:
https://doaj.org/article/7b50fe8673124ad8bbc8f09a875ed746
Autor:
Gülnihal Kutlu, Fatma Genç, Yasemin Ünal, Dilek Aslan Öztürk, Abidin Erdal, Yasemin Biçer Gömceli
Publikováno v:
Türk Uyku Tıbbı Dergisi, Vol 5, Iss 1, Pp 12-16 (2018)
Objective: Restless Legs syndrome (RLS) is a frequent neurological disease. Levetiracetam (LEV) is an effective and broad-spectrum anticonvulsant drug. The aim of this study is to investigate the frequency of RLS in patients diagnosed with epilepsy
Externí odkaz:
https://doaj.org/article/f75fb50a536042919926ba57a847a552
Publikováno v:
Archives of Epilepsy, Vol 22, Iss 2, Pp 55-60 (2016)
Objectives:Psychogenic nonepileptic seizures (PNES) resemble epileptic seizures. Accurate diagnosis of PNES can be challenging, and misdiagnosis and treatment confusion is common. This article is a review of patients with PNES who were initially diag
Externí odkaz:
https://doaj.org/article/11c25b4ab50f4931ac1b0be9365c2fa7
Autor:
Abidin ERDAL, Aylin BİCAN DEMİR, İpek MİDİ, Yasemin BİÇER GÖMCELİ, Gülnihal KUTLU, S. Naz YENİ, İbrahim BORA
Publikováno v:
Archives of Epilepsy, Vol 22, Iss 1, Pp 12-16 (2016)
Objectives:Neurocutaneous syndromes are genetic diseases that affect the nervous system and the skin. Epileptic seizures are seen with variable frequency. In the present study, data of 29 patients from 5 centers were analyzed in an effort to draw att
Externí odkaz:
https://doaj.org/article/4a4ae5e5cee64bfc836bbbf540c9c7f8
Autor:
Eylem ÖZAYDIN GÖKSU, Fatma GENÇ, Burcu YÜKSEL, Elif SARIÖNDER GENCER, Abidin ERDAL, Yasemin BİÇER GÖMCELİ
Publikováno v:
Archives of Epilepsy, Vol 21, Iss 3, Pp 111-118 (2015)
Objectives:The aim of the present study was to determine demographic properties and risk factors for early- and late-onset seizures, as well as the effects of these factors on prognosis of patients with post-stroke epilepsy.Methods:Only patients with
Externí odkaz:
https://doaj.org/article/c4d0c6be7c824ba59640fde6528cc231
Autor:
Abidin ERDAL, Yasemin AYDEMİR, F. Ezgi UÇAN TOKUÇ, Gizem ÖZDEMİR, Gülnihal KUTLU, Fatma GENÇ, Yasemin BİÇER GÖMCELİ
Publikováno v:
Archives of Epilepsy, Vol 21, Iss 2, Pp 81-85 (2015)
The drug rufinamide was approved in November 2008 by the US Food and Drug Administration for use in the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in patients older than 4 years. Lennox-Gastaut Syndrome is one of the mos
Externí odkaz:
https://doaj.org/article/169cf2d2249d466290c5cce46f4a3617
Publikováno v:
Türk Nöroloji Dergisi, Vol 16, Iss 1, Pp 40-46 (2010)
Lafora disease is a typical progressive myoclonic epilepsy that is characterized by autosomal recessive inheritance, myoclonic and occipital seizures, progressive dementia, ataxia, and dysarthria. Two siblings with myoclonic and generalized tonic clo
Externí odkaz:
https://doaj.org/article/2d281bced29448829b2bddb81f0ec284