Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Kemal TUTKAVUL"'
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Myasthenia gravis (MG) is a disorder of the neuromuscular junction that can deteriorate into myasthenic crisis, involving weakness of bulbar and respiratory muscles. In this study, we describe the clinical manifestations of myasthenic crisis, identif
Externí odkaz:
https://doaj.org/article/c70041f17ce94be3a9d88fe601029fc2
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 38, Iss 2, Pp 127-134 (2021)
Objective: The increase in the average life expectancy of humans has resulted in an increased occurrence of late-onset myasthenia gravis (LOMG). It is noticeable that the clinical, immunologic, and prognostic features of patients with LOMG are differ
Externí odkaz:
https://doaj.org/article/73a9277f235649e39f12e556d543b9db
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 5, Pp 452-459 (2020)
OBJECTIVE: Myasthenia gravis (MG) is an autoimmune disease that may cause a disorder in transmission at the neuromuscular junction. Antibodies directed against acetylcholine receptors are responsible. The thymus is the place that that production of t
Externí odkaz:
https://doaj.org/article/f01060ee596c41b0ae52a54d642d1d97
Publikováno v:
Archives of Epilepsy, Vol 25, Iss 3, Pp 117-122 (2019)
Objectives:Epilepsy is the second most common neurological disorder after migraine in pregnancy. The most suitable antiepileptic drug (AED) to be chosen in this period would minimize the possible maternal and fetal complications. The present study mo
Externí odkaz:
https://doaj.org/article/4d14ba042e5a4eb796416766d11969c1
Autor:
Buse Rahime Hasırcı Bayır, Kemal Tutkavul, Yılmaz Çetinkaya, İbrahim Anıl Tuncer, Hülya Tireli
Publikováno v:
Türk Nöroloji Dergisi, Vol 24, Iss 3, Pp 275-276 (2018)
Externí odkaz:
https://doaj.org/article/37dc480b9b5b4800917bc40d713d84f8
Publikováno v:
Türk Nöroloji Dergisi, Vol 14, Iss 2, Pp 128-131 (2008)
Scientific BACKGROUND: Dropped head sing is characterized by severe neck flexion. It results from neck extensor weakness or increased tone of the flexor muscles. This sign is usually reported in neuromuscular diseases such as amyotrophic lateral scle
Externí odkaz:
https://doaj.org/article/d37b6696565d40739381f6a211d03f5e
Autor:
Nermin Görkem Sirin, Volkan Tasdemir, Arman Cakar, Ayla Culha, Aysun Soysal, Ayse Deniz Elmali, Aysegül Gündüz, Destina Yalcin, Dilek Atakli, Elif Kocasoy Orhan, Erdem Tüzün, Eren Gözke, Esra Gürsoy, Feray Karaali Savrun, Ferda Ilgen Uslu, Fikret Aysal, Hacer Durmus, Hafsa Bülbül, F.Inci Ertas, Kayıhan Uluc, Kemal Tutkavul, Leyla Baysal, Mehmet Baris Baslo, Meral Kiziltan, Metin Mercan, Nevin Pazarci, Nurten Uzun, Onur Akan, Ozlem Cokar, Pinar Kahraman Koytak, Reyhan Sürmeli, Sefer Günaydin, Selahattin Ayas, Sezin Alpaydın Baslo, Vildan Yayla, Vuslat Yilmaz, Yesim Parman, Zeliha Matur, Zeynep Unlüsoy Acar, Ali Emre Oge
Publikováno v:
Clinical Neurophysiology. 141:S127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2edd891659676c957553dd4839c42a9
https://doi.org/10.1016/j.clinph.2022.07.333
https://doi.org/10.1016/j.clinph.2022.07.333
Autor:
Betül Baykan, Ugur Ozbek, Seda Süsgün, Yesim Kesim, Sibel Aylin Ugur Iseri, Kemal Tutkavul, Ozkan Ozdemir, Emrah Yücesan, Nerses Bebek, Semih Ayta, Aysin Dervent, Garen Haryanyan, Barış Salman, Cigdem Ozkara
Lafora disease (LD) is a severe form of progressive myoclonus epilepsy inherited in an autosomal recessive fashion. It is associated with biallelic pathogenic variations in EPM2A or NHLRC1, which encode laforin and malin, respectively. The disease us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9de5b71b3953fbd4addcaf7aa13b2a30
http://hdl.handle.net/20.500.12645/28987
http://hdl.handle.net/20.500.12645/28987
Autor:
Kemal Tutkavul, Yılmaz Çetinkaya
Publikováno v:
Volume: 49, Issue: 2 635-638
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: This study aimed to reveal the optimum recording time of routine electroencephalogram (EEG) for adults with epilepsy.Materials and methods: In this clinical observational study we investigated features of paroxysms that emerged in EEG
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b2fdb7157d756ec42c57a15d773e8e
https://doi.org/10.3906/sag-1810-117
https://doi.org/10.3906/sag-1810-117
Autor:
Garen, Haryanyan, Ozkan, Ozdemir, Kemal, Tutkavul, Aysin, Dervent, Semih, Ayta, Cigdem, Ozkara, Baris, Salman, Emrah, Yucesan, Yesim, Kesim, Seda, Susgun, Ugur, Ozbek, Betul, Baykan, Sibel A, Ugur Iseri, Nerses, Bebek
Publikováno v:
Journal of human genetics. 66(12)
Lafora disease (LD) is a severe form of progressive myoclonus epilepsy inherited in an autosomal recessive fashion. It is associated with biallelic pathogenic variations in EPM2A or NHLRC1, which encode laforin and malin, respectively. The disease us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81a17b8dec85d8960d0d8f1e9390ce93
https://pubmed.ncbi.nlm.nih.gov/34117373
https://pubmed.ncbi.nlm.nih.gov/34117373