Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Fatma, Candan"'
Publikováno v:
Journal of Ankara University Faculty of Medicine / Ankara Üniversitesi Tip Fakültesi Mecmuasi; 2024, Vol. 77 Issue 2, p122-127, 6p
Publikováno v:
Issue: 51 411-442
Türkiye Adalet Akademisi Dergisi
Türkiye Adalet Akademisi Dergisi
The legal relationship between medical doctors, foundation hospitals, and patients has been discussed in the legal doctrine and numerous court decisions. Yet, there is no consensus on the description and legal characteristic of that relationship. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a98596cf782f34ee87c2757661a153b
https://doi.org/10.54049/taad.1140190
https://doi.org/10.54049/taad.1140190
Publikováno v:
Archives of Epilepsy, Vol 21, Iss 2, Pp 76-80 (2015)
Objectives:This study aimed to compare seizure types, clinical and demographic features, treatment response and prognosis among patients with early and late onset post-stroke seizures.Methods:A retrospective evaluation was made of the data of 46 pati
Externí odkaz:
https://doaj.org/article/65345d70d0c547fc8e0b72ab74ae25e0
Autor:
Adile ÖZKAN, Fatma CANDAN, İlknur AYDIN CANTÜRK, Sevda Yıldız GÖKÇEER, Nihal IŞIK, Handan Işın ÖZIŞIK KARAMAN
Publikováno v:
Archives of Epilepsy, Vol 21, Iss 2, Pp 54-58 (2015)
Objectives:Epilepsy is one of the most common serious neurological disorders in the elderly. In this study the demographic and clinical features, etiological factors, seizure types and response ratios to treatment are presented for a group of patient
Externí odkaz:
https://doaj.org/article/9e50cbeb71a842459b09e2fb540e6b61
Publikováno v:
Türk Nöroloji Dergisi, Vol 21, Iss 4, Pp 154-158 (2015)
Objective: Although essential tremor (ET) is the most common movement disorder, its pathogenesis is poorly understood. It is suggested that the ventral intermediate (VIM) nucleus of the thalamus is important in the pathophysiology disease. Material
Externí odkaz:
https://doaj.org/article/f95355b36a6e421a8a1e70fe87607c6a
Autor:
Tuba Cerrahoglu, Sirin, Zerrin, Karaaslan, Burcu N, Arkali, Pınar, Bekdik, Tuba, Akinci, Fatma, Candan, Emel Oguz, Akarsu, M Baris, Baslo, Elif Kocasoy, Orhan, A Emre, Oge
Publikováno v:
Neurology India.
The aim of this study was to evaluate the contribution of extraocular muscle function testing with video-oculography (VOG), which is a noninvasive and easily applicable method of recording eye movement with digital cameras, to the diagnosis of myasth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2097976ffc6248a8336d9647504d3be
https://doi.org/10.4103/0028-3886.336330
https://doi.org/10.4103/0028-3886.336330
Publikováno v:
Türk Nöroloji Dergisi, Vol 13, Iss 6, Pp 409-414 (2007)
OBJECTIVE: Peroxynitrite (PRN) is a strong oxidant capable of damaging tissues and cells, and plays a major role in the pathogenesis of multiple sclerosis (MS). Uric acid (UA) is the naturally occuring final product of the purine metabolism in humans
Externí odkaz:
https://doaj.org/article/62d0f386e6f44224936b10e843187b83
Publikováno v:
Türk Nöroloji Dergisi, Vol 13, Iss 5, Pp 305-309 (2007)
OBJECTIVE: Leukoaraiosis (LA), is a radiological finding with bilateral, either patchy or diffuse areas of the cerebral white matter.We aimed to determine proton MRS findings of LA and compare to those with chronic ischemic infarcts and control subje
Externí odkaz:
https://doaj.org/article/ccdc9d32c83a4d65b03fc89d82674c29
Publikováno v:
Türk Nöroloji Dergisi, Vol 13, Iss 5, Pp 325-332 (2007)
OBJECTIVE: Multipl sclerosis is characterized by the destruction myelin and lipid metabolism occuring in central nervous system. OBJECTIVES: The present study was planned to investigate the relationship between the plasma lipid profile and disease a
Externí odkaz:
https://doaj.org/article/ddcdbf7abafb4044a850ea4122f452ea
Autor:
Mary M. Reilly, Mahima Kapoor, Zhongbo Chen, Onur Akan, Mert Karakaya, Reza Maroofian, Seena Vengalil, Brunhilde Wirth, Veeramani Preethish-Kumar, Stephan Züchner, Bevinahalli N Nandeesh, Stephanie Efthymiou, Mina Ryten, Bertold Schrank, Henry Houlden, David Murphy, Atchayaram Nalini, Emil K. Gustavsson, Fatma Candan, Leena Shingavi, A. Nazli Basak, Nalan Gökçe Güneş, Leyla Meier, Payam Sarraf, Kiran Polavarapu
BACKGROUND AND PURPOSE Pathogenic variants in PLEKHG5 have been reported to date to be causative in three unrelated families with autosomal recessive intermediate Charcot-Marie-Tooth disease (CMT) and in one consanguineous family with spinal muscular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb14979112bd133b5cc127b106a0383
https://openaccess.sgul.ac.uk/id/eprint/112664/1/ene.14649.pdf
https://openaccess.sgul.ac.uk/id/eprint/112664/1/ene.14649.pdf
