Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Pelin Albayrak"'
Autor:
Muhammet G Kutluk, Naz Kadem, Omer Bektas, Nadide C Randa, Gökcen O Tuncer, Pelin Albayrak, Tuba Eminoglu, Serap T Teber
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 4, Pp 547-551 (2021)
Objectives: Collagen-VI-related myopathies are caused by both dominant and recessive mutations in the three collagen-VI-related genes (COL6A1, COL6A2, and COL6A3) and present as two different major clinical entities; Bethlem myopathy and Ullrich cong
Externí odkaz:
https://doaj.org/article/8615e6f956ee4f19be87bcb3d1ffb15f
Autor:
M Gultekin Kutluk, Naz Kadem, Omer Bektas, Nadide Cemre Randa, Gökcen O Z Tuncer, Pelin Albayrak, Tuba Eminoglu, Serap Tiras Teber
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Externí odkaz:
https://doaj.org/article/8d171ea81d474ee1b49da4d9f1020518
Autor:
Pelin ALBAYRAK FAKIOĞLU
Publikováno v:
Volume: 15, Issue: 2 861-878
Kent Akademisi
Kent Akademisi
Küreselleşme ve neoliberalizm ile birlikte ülkelerin kalkınma politikalarında ve bölge planlamalarında farklılıklar oluşmuş, yeni teoriler ve politikalar gündeme gelmiştir. Özellikle neoliberal politikaların yoğun bir şekilde hissedi
Autor:
Dilşa Cemre Akkoç, Gökçen Öz Tunçer, Pelin Albayrak, Gülhis Deda, Muhammed Gültekin Kutluk, Serap Teber
Publikováno v:
Turkish Journal of Pediatric Disease. :1-5
Amac: Hastanemize herhangi bir nedenle basvuran hastalarin yakinlarinin febril konvulziyon hakkindaki bilgi, kaygi ve dusunceleri degerlendirilmesi amaclanmistir. Gerec ve Yontemler: Calismaya 18-70 yas arasi 600 katilimci alindi. Katilimcilarin yas,
Autor:
Ömer Bektaş, Gökçen Öz Tunçer, M Gultekin Kutluk, Nadide Cemre Randa, Serap Teber, Pelin Albayrak, Tuba F. Eminoglu, Naz Kadem
Publikováno v:
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Autor:
Mehmet Sertac Alpaydin, Ahmet Lütfü Sertdemir, Pelin Albayrak, Mehmet Akif Bor, Sami Erdem, Zafer Buyukterzi, Kadri Murat Gurses
Publikováno v:
Kocaeli Medical Journal. 8:74-80
Autor:
Nadide Cemre Randa, Muhammet Gültekin Kutluk, Serap Teber, Tuba F. Eminoglu, Gökçen Öz Tunçer, Naz Kadem, Ömer Bektaş, Pelin Albayrak
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 4, Pp 547-551 (2021)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Objectives Collagen-VI-related myopathies are caused by both dominant and recessive mutations in the three collagen-VI-related genes (COL6A1, COL6A2, and COL6A3) and present as two different major clinical entities; Bethlem myopathy and Ullrich conge
Autor:
Pelin Albayrak, Gökçen Öz Tunçer, Gülhis Deda, Pınar Haznedar, Özlem Doğan, F. Tuba Eminoglu, Serap Teber
Publikováno v:
Epilepsy research. 153
Background and aims The relationship between anti-epileptic usage and oxidative damage has not yet been clearly understood. In our study, we investigated oxidative stress parameters, carnitine levels, liver function tests (LFT) and their relationship
Dravet syndrome is a catastrophic progressive epileptic syndrome. De novo loss of function mutations on the SCN1A gene coding voltage-gated sodium channels are responsible. Disruption of the triggering of hippocampal GABAergic interneurons is assumed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48f2503fc58311fa7d592e838ab76f8f
https://europepmc.org/articles/PMC6408181/
https://europepmc.org/articles/PMC6408181/
Autor:
Ömer Bektaş, Muhammet Gültekin Kutluk, Serap Teber, Gökçen Öz Tunçer, Pınar Haznedar, Naz Kadem, Pelin Albayrak
Publikováno v:
Acta neurologica Belgica. 119(4)
Hashimoto's encephalopathy (HE) is a rare, poorly understood, progressive and relapsing, steroid-responsive multiform disease. HE presents with subacute cognitive dysfunction, psychiatric symptoms, seizures, and movement disorders. The disorder is us