Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Tülay Kurt"'
Autor:
Ebru Boluk, Cansu Uzunoğlu, Yaprak Seçil, Yusuf Kenan Çetinoğlu, Şehnaz Arıcı, Mustafa Fazıl Gelal, Tülay Kurt-İncesu
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 38, Iss 3, Pp 151-157 (2021)
Objectives: Patients are frequently referred to electrophysiology laboratories by physicians from various specialties with a presumptive diagnosis of radiculopathy. Recent advances in spinal imaging techniques have led to an increase in magnetic reso
Externí odkaz:
https://doaj.org/article/afa6eb874e3a48ad8d63dff314cd593d
Publikováno v:
Archives of Epilepsy, Vol 26, Iss 2, Pp 72-80 (2020)
Objectives:This study aims to determine the prevalence of lateralized semiological findings in patients with temporal lobe epilepsy and to assess the contribution of relatively rare symptoms to lateralization, as well as classical lateralizing findin
Externí odkaz:
https://doaj.org/article/6f4c807f786d4577b19477d1d3c54154
Autor:
Hülya Uluğut Erkoyun, Sevgin Gündoğan, Yaprak Seçil, Yeşim Beckmann, Tülay Kurt İncesu, Hatice Sabiha Türe, Galip Akhan
Publikováno v:
Türk Nöroloji Dergisi, Vol 24, Iss 1, Pp 63-69 (2018)
Paraneoplastic neurologic syndromes (PNS) are rare disorders, which are remote effects of cancer that are not caused by the tumor, its metastasis or side effects of treatment. We had nine patients with PNS; two of our patients had limbic encephalitis
Externí odkaz:
https://doaj.org/article/274ff89844314841a80e2efbeb2cc401
Publikováno v:
Türk Yoğun Bakim Derneği Dergisi, Vol 12, Iss 3, Pp 110-117 (2014)
Neuroleptic malignant syndrome (NMS) is a rare but life-threatening clinical manifestation induced by neuroleptic medication. Although NMS is regarded as a psychiatric diagnosis, its treatment requires a systematic approach and thus intensive care fo
Externí odkaz:
https://doaj.org/article/f3b7e8c1715d47b6afc236d44dc21bea
Autor:
Gulden Diniz, Yaprak Secil, Serdar Ceylaner, Figen Tokucoglu, Sabiha Türe, Mehmet Celebisoy, Tülay Kurt İncesu, Galip Akhan
Publikováno v:
Case Reports in Neurological Medicine, Vol 2016 (2016)
Background. Hereditary inclusion body myopathy is caused by biallelic defects in the GNE gene located on chromosome 9p13. It generally affects adults older than 20 years of age. Methods and Results. In this study, we present two Turkish sisters with
Externí odkaz:
https://doaj.org/article/f06f65412b59449f98efd0694914db09
Autor:
Erkoyun, Hülya Uluğut, Beckmann, Yeşim, Bülbül, Nazlı Gamze, İncesu, Tülay Kurt, Kanat, Nevin Gürgör, Ertekin, Cumhur
Publikováno v:
In Multiple Sclerosis and Related Disorders October 2017 17:179-183
Autor:
Seçil, Yaprak, Arıcı, Şehnaz, İncesu, Tülay Kurt, Gürgör, Nevin, Beckmann, Yeşim, Ertekin, Cumhur
Publikováno v:
In Neurophysiologie Clinique / Clinical Neurophysiology June 2016 46(3):171-178
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Publikováno v:
Izmir Katip Celebi University Faculty of Medicine. 1:7-10
BACKGROUND Aphasia is one of the most common neurological symptoms after stroke and often results in significant disability. The intensity and duration of speech and language therapy are often confounded. OBJECTIVE The aim of this study to evaluate t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e479c35a9bb4f6566424de8528af2845
https://doi.org/10.52818/cjmrtu.2021.2
https://doi.org/10.52818/cjmrtu.2021.2
Autor:
Seçil, Yaprak, Ekinci, Ayşen Süzen, Bayram, Korhan Barış, İncesu, Tülay Kurt, Tokuçoğlu, Figen, Gürgör, Nevin, Özdemirkıran, Tolga, Başoğlu, Mustafa, Ertekin, Cumhur
Publikováno v:
In Clinical Neurophysiology September 2012 123(9):1831-1835