Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Demet ÖZBABALIK ADAPINAR"'
Publikováno v:
Türk Nöroloji Dergisi, Vol 26, Iss 3, Pp 212-219 (2020)
Objective: The objective of this research was to compare the verbal fluency skills of patients diagnosed as having amnestic mild cognitive impairment (aMCI) with the participants without neurologic or psychiatric problems through quantitative and qua
Externí odkaz:
https://doaj.org/article/8886ecfff24b47e1a5d94a74c9b4e032
Autor:
Türkan Acar, Esra Acıman Demirel, Nazire Afşar, Aylin Akçalı, Gülşen Akman Demir, Aybala Neslihan Alagöz, Tuğçe Angın Mengi, Ethem Murat Arsava, Semih Ayta, Nerses Bebek, Başar Bilgiç, Cavit Boz, Arman Çakar, Neşe Çelebisoy, Mehmet Uğur Çevik, Firuze Delen, Hacer Durmuş Tekçe, Hakan Ekmekçi, Ayşe Deniz Elmalı, Oğuz Osman Erdinç, Füsun Ferda Erdoğan, Fettah Eren, Ufuk Ergün, Yeşim Gülşen Parman, Haluk Gümüş, Demet İlhan Algın, Rana Karabudak, Ömer Karadaş, Özlem Kayım Yıldız, Emine Rabia Koç, Demet Özbabalık Adapınar, Atilla Özcan Özdemir, Şerefnur Öztürk, Ayşe Sağduyu Kocaman, Şevki Şahin, Esen Saka Topçuoğlu, Özden Şener, F. İrsel Tezer, Rıfat Erdem Toğrol, Ayşe Bora Tokçaer, Mehmet Akif Topçuoğlu, Neşe Tuncer, Ali Ulvi Uca, Kayıhan Uluç, Erdem Yaka, Mehmet İlker Yön
Publikováno v:
Türk Nöroloji Dergisi, Vol 26, Iss 2, Pp 58-108 (2020)
Externí odkaz:
https://doaj.org/article/9e059a592187495c841789571449a527
Autor:
Demet Özbabalık Adapınar, Suzan Saylısoy, Çınar Yenilmez, Hüseyin Aslan, Bengü Ertan, Sevilhan Artan, Gülcan Güleç, Çiğdem Susuz, Baki Adapınar
Publikováno v:
Dementia and Geriatric Cognitive Disorders Extra, Vol 1, Iss 1, Pp 429-432 (2011)
Variant Creutzfeldt-Jakob disease (vCJD) was first reported in the UK in 1996. Here, we report the first Turkish case of vCJD. A 47-year-old man, who has never lived outside of Turkey and had had no transfusion, was admitted to the University Hospita
Externí odkaz:
https://doaj.org/article/4058f0b167f845abb7a6787905e3fb3a
Publikováno v:
Türk Nöroloji Dergisi, Vol 17, Iss 1, Pp 62-63 (2011)
Externí odkaz:
https://doaj.org/article/f425e7c135f24b8c966356b8bd6aa0d8
Publikováno v:
Archives of Epilepsy, Vol 23, Iss 1, Pp 35-39 (2017)
Nonconvulsive status epilepticus (NCSE) is characterized by unexplained changes in behavioral and mental status accompanied by a continuous seizure activity seen on electroencephalography. The treatment is similar to that of status epilepticus. Lacos
Externí odkaz:
https://doaj.org/article/d1ef3843c00e4f4fb281115bac7c169e
Frontotemporal dementia (FTD) is a clinically, neuropathologically, and genetically heterogeneous disorder. About 30%–40% of cases diagnosed with FTD have positive family history. MAPT, GRN, C9orf72 genes play significant roles in development of di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61996b47e041436e2ad74c2a05919077
https://doi.org/10.1016/b978-0-12-817990-1.00001-9
https://doi.org/10.1016/b978-0-12-817990-1.00001-9
Publikováno v:
The Turkish Journal of Geriatrics. 21:208-216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b300a965265d7736deb13cde85db2dd
https://doi.org/10.31086/tjgeri.2018240421
https://doi.org/10.31086/tjgeri.2018240421
Autor:
Ebru Erzurumluoğlu Gökalp, Oguz Cilingir, Serhat Özkan, Sinem Kocagil, Belgin Demet Özbabalik Adapinar, Muzaffer Bilgin, Sevilhan Artan, Konül Haziyeva, Serap Arslan, Beyhan Durak Aras
Publikováno v:
OSMANGAZİ JOURNAL OF MEDICINE.
Alzheimer’s disease (AD) is a progressive neurodegenerative disease and the most common form of the dementia which is characterized by the accumulation of amyloid plaques at the extracellular compartment and formation of neurofibriller tangles at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98a7042d18005143b424c23524398e84
https://doi.org/10.20515/otd.553900
https://doi.org/10.20515/otd.553900
Autor:
Hulya Ozen, Sinem Kocagil, Oguz Cilingir, Sevilhan Artan, Belgin Demet Özbabalik Adapinar, Ebru Erzurumluoglu, Başar Bilgiç, Çınar Yenilmez, Beyhan Durak Aras
Publikováno v:
Neurobiology of aging. 76
Frontotemporal lobar degeneration (FTLD) describes a group of progressive brain disorders. The expansion of a noncoding GGGGCC (G(4)C(2)) hexanucleotide repeat in the C9orf72 gene is a major cause of both familial FTLD and amyotrophic lateral scleros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ba6c99ead947c6eaaee4725075c0a1
https://pubmed.ncbi.nlm.nih.gov/30685122
https://pubmed.ncbi.nlm.nih.gov/30685122
Publikováno v:
Archives of Epilepsy, Vol 29, Iss 1, Pp 34-36 (2023)
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is a hereditary disease of cerebral microvessels with autosomal dominant inheritance due to the NOTCH3 gene mutation. Epileptic seizures were observe
Externí odkaz:
https://doaj.org/article/f3eee7764b99440781e8fb3c39c1c55f