Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sefer Günaydın"'
Autor:
Berrin Pelit Uzunalimoğlu, Abdülhamit Sağlam, Büşra Şişman, Sefer Günaydın, Esen Gül Uzuner, Fikret Aysal, Erdem Tüzün, Birgül Baştan
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 2, Pp 549-554 (2021)
Epstein-Barr virus (EBV) has been associated with a plethora of neurological manifestations including polyneuropathy and polyradiculopathy. A 27-year-old man with a recent upper respiratory system infection presented with difficulty in walking. His n
Externí odkaz:
https://doaj.org/article/af9e9bceac404d61a8ddb1da5da01595
Autor:
Miray Atacan Yaşgüçlükal, Cansu Tunç, Muhammet Duran Bayar, Birgül Baştan, Sefer Günaydın, Belgin Petek Balcı, Özlem Çokar
Publikováno v:
Türk Nöroloji Dergisi, Vol 27, Iss 1, Pp 85-87 (2021)
Anti-glutamic acid decarboxylase antibodies (anti-GAD-ab) are associated with various neurologic conditions. High titers of anti-GAD-abs are observed in stiff person syndrome and subacute cerebellar degeneration. Type 1 diabetes mellitus (T1DM) and o
Externí odkaz:
https://doaj.org/article/8de6c6ca7f8c474c9a22b003616ae204
Publikováno v:
Haseki Tıp Bülteni, Vol 53, Iss 4, Pp 308-312 (2015)
Tolosa-Hunt syndrome (THS) is a painful ophthalmoplegia, characterized by cryptogenic granulomatous inflammation of the cavernous sinus and/or superior orbital fissure. Glucocorticoid treatment is used for both diagnostic and therapeutic purposes. Ac
Externí odkaz:
https://doaj.org/article/1ea1cd93888543c5aea48cc98606e998
Autor:
Emel Oğuz Akarsu, Hürtan Acar, Feriha Ozer, Sefer Günaydın, Özger Akarsu, Tuba Aydemir Özcan, Serkan Özben, Aytul Mutlu, Mithat Bedir, Gülsün Çınarlı Gül, Özlem Çokar, Mehmet Burak Aktuğlu
Publikováno v:
Türk Nöroloji Dergisi, Vol 19, Iss 4, Pp 128-133 (2013)
OBJECTIVE: Hypothyroidism may cause neurologic signs and symptoms as its effects neuromuscular system like many other systems. Subclinical hypothyroidism is the most common thyroid dysfuntion, it may cause neuromuscular signs and symptoms. In this re
Externí odkaz:
https://doaj.org/article/298680b9ece445b7898599fad696badd
Publikováno v:
Türk Nöroloji Dergisi, Vol 12, Iss 1, Pp 50-58 (2006)
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxia, myoclonic jerks together with pyramidal and extrapyramidal signs. It is a rare prion disease and definitive diagnosis can only be made by biopsy.
Externí odkaz:
https://doaj.org/article/21dfc4cb2ec549e2addd84969101e88f