Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Meliha Tan"'
Autor:
Soner Solmaz, Çiğdem Gereklioğlu, Meliha Tan, Şenay Demir, Mahmut Yeral, Aslı Korur, Can Boğa, Hakan Özdoğu
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 4, Pp 367-370 (2015)
Thiamine is a water-soluble vitamin. Thiamine deficiency can present as a central nervous system disorder known as Wernicke's encephalopathy, which classically manifests as confusion, ataxia, and ophthalmoplegia. Wernicke's encephalopathy has rarely
Externí odkaz:
https://doaj.org/article/2e42b7a1decf4696b336f15f92a250a1
Publikováno v:
Türk Nöroloji Dergisi, Vol 15, Iss 3, Pp 140-144 (2009)
Hypnic headache is a primary, rare headache disorder of the elderly, which occurs during sleep. Polysomnography (PSG) studies have shown that hypnic headache occurs with much gretaer frequency during REM sleep than during non-REM sleep. We present a
Externí odkaz:
https://doaj.org/article/9eb9a1f05a284d84a8d54c678a6f7bf2
Autor:
Asuman Çelikbilek, Mehmet Çelikbilek, Alper Bozkurt, Başak Karakurum Göksel, Meliha Tan, Hakan Özdoğu
Publikováno v:
Case Reports in Neurology, Vol 1, Iss 1, Pp 15-19 (2009)
We report a 20-year-old woman with sickle cell disease (SCD) who presented with a severe pulsating headache, nausea, and vomiting. Her history was significant for a past thrombotic event during which she had not used anticoagulation therapy as prescr
Externí odkaz:
https://doaj.org/article/2975b6e1d1474bd09ace95d76ef93119
Publikováno v:
Türk Nöroloji Dergisi, Vol 15, Iss 1, Pp 39-43 (2009)
The cortical motor hand area is a knob-like structure of the precentral gyrus, with an inverted omega or horizontal epsilon shape. Isolated hand weakness is infrequently observed and is usually due to small cortical infarcts of this hand knob structu
Externí odkaz:
https://doaj.org/article/107be2739e2643068438904ffa4f6f54
Publikováno v:
Journal of Radiology Case Reports, Vol 3, Iss 3, Pp 25-28 (2009)
Guillain-Barré syndrome is a relatively common, acute, and rapidly progressive, inflammatory demyelinating polyneuropathy. The diagnosis is usually established on the basis of symptoms and signs, aided by cerebrospinal fluid findings and electrophys
Externí odkaz:
https://doaj.org/article/4b7f4d55ddf9484ba061369eb95339e6
Publikováno v:
Turkiye Klinikleri Journal of Neurology. 10:76-80
Autor:
Başak Karakurum Göksel, Ahmet Eftal Yücel, Meliha Tan, Emine Duygu Ersozlu Bozkirli, Sibel Karaca
Publikováno v:
Nöro Psikiyatri Arşivi. 51:148-156
Introduction Neurological involvements were shown in 20% of patients with Primary Sjogren's Syndrome (pSS). Neurological symptoms may be the first signs of pSS in 57% of the cases. In addition, early diagnosis and treatment of neurological disorders
Autor:
Sibel Karaca, V. Deniz Yerdelen, Meliha Tan, Başak Karakurum Göksel, Zulfikar Arlier, Ilknur Kozanoglu, Semih Giray, Mehmet Karataş
Publikováno v:
Nöro Psikiyatri Arşivi. 51:63-68
Introduction In this study, we report the results of our experience of therapeutic plasma exchange (TPE) for neuroimmunologic disorders performed at our hospital over a seven-year period. Methods We retrospectively reviewed the medical records of 91
Publikováno v:
Volume: 46, Issue: 3 834-839
Turkish Journal of Medical Sciences
Turkish Journal of Medical Sciences
Background/aim: The aim of this study was to evaluate perfusion computed tomography (PCT) findings in patients with Alzheimer disease and to compare them with those of patients without dementia. Materials and methods: PCT was performed in 35 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::003b80c91f701550e0b6e116746f8175
http://hdl.handle.net/11727/3903
http://hdl.handle.net/11727/3903
Autor:
Haluk Topaloglu, Aslihan Ors, Suleyman Gulsuner, Huseyin Boyaci, O Emre Onat, A. Nazli Basak, Murat Gunel, Katja Doerschner, Kaya Bilguvar, Tayfun Ozcelik, Ayse B. Tekinay, Hilal Unal, Üner Tan, Meliha Tan, Ergin Atalar, Tulay Kansu
Publikováno v:
Genome Research
The biological basis for the development of the cerebro-cerebellar structures required for posture and gait in humans is poorly understood. We investigated a large consanguineous family from Turkey exhibiting an extremely rare phenotype associated wi