Yavuz Selvi, P. Özdemir, Abdullah Atli̇, Lütfullah Beşiroğlu
{"title":"Nöropsikiyatrik Belirtilerle İlişkili Tüberküloz Lenfadenit: Bir Katatoni Olgusu","authors":"Yavuz Selvi, P. Özdemir, Abdullah Atli̇, Lütfullah Beşiroğlu","doi":"10.4274/NPA.Y5768","DOIUrl":"https://doi.org/10.4274/NPA.Y5768","url":null,"abstract":"","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"68 1","pages":"265-267"},"PeriodicalIF":1.1,"publicationDate":"2011-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90939453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mehmet Fatih Ceylan, Salih Selek, Esra Zeytinci, Haluk A. Savaş
{"title":"Streptokok enfeksiyonu sonrasi{dotless}nda gelişen myoklonik belirtilerle seyreden bir olgu sunumu: Olasi{dotless} PANDAS varianti{dotless}","authors":"Mehmet Fatih Ceylan, Salih Selek, Esra Zeytinci, Haluk A. Savaş","doi":"10.4274/NPA.Y5614","DOIUrl":"https://doi.org/10.4274/NPA.Y5614","url":null,"abstract":"","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"15 1","pages":"85-87"},"PeriodicalIF":1.1,"publicationDate":"2011-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86637722","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A. Tahiroğlu, G. Çelik, Cigil Fettahoglu, Veli Yıldırım, Fevziye Toros, A. Avci, Esin Ozatalay, Mehtap Uzel
{"title":"Psikiyatrik bozukluğu olan ve olmayan ergenlerde problemli internet kullanımı","authors":"A. Tahiroğlu, G. Çelik, Cigil Fettahoglu, Veli Yıldırım, Fevziye Toros, A. Avci, Esin Ozatalay, Mehtap Uzel","doi":"10.4274/NPA.5452","DOIUrl":"https://doi.org/10.4274/NPA.5452","url":null,"abstract":"","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"63 1","pages":"241-246"},"PeriodicalIF":1.1,"publicationDate":"2011-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91093173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Antiepileptik ilaçların lipit profili ve karaciğer enzimleri üzerine etkisi","authors":"Nermin Bölükbaşı, Ferda Akar, L. S. Bir","doi":"10.4274/NPA.Y5513","DOIUrl":"https://doi.org/10.4274/NPA.Y5513","url":null,"abstract":"","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"192 1","pages":"11-16"},"PeriodicalIF":1.1,"publicationDate":"2011-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72825391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aysun Kalenderoǧlu, Haluk A. Savaş, H. S. Gergerlioğlu, Kemal Başaralı, Mehmet Yumru, Salih Selek, Sadik Buyukbas, Neyhan Ergene
{"title":"Bipolar Hastalarda Serum Ghrelin Seviyeleri ve Metabolik Sendrom Arasi{dotless}ndaki İlişki","authors":"Aysun Kalenderoǧlu, Haluk A. Savaş, H. S. Gergerlioğlu, Kemal Başaralı, Mehmet Yumru, Salih Selek, Sadik Buyukbas, Neyhan Ergene","doi":"10.4274/NPA.Y5648","DOIUrl":"https://doi.org/10.4274/NPA.Y5648","url":null,"abstract":"","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"72 1","pages":"328-332"},"PeriodicalIF":1.1,"publicationDate":"2011-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72788994","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. Yavuz, A. Demirkan, Sanne Moen, Ö. Özdemir, Suzin Çatal, N. Bebek, U. Ozbek, B. Baykan
Objective: Although photosensitive epilepsy (PE) is commonly observed, its pathophysiology has not been clarified yet. However, relevant literature indicates that genetic factors play an important role. Our aim was to investigate whether there is a relationship between the clinical and electroencephalographic (EEG) features and the possible mutations/polymorphisms in the GABA receptor alpha 1 subunit (GABRA1) gene in patients with PE by scanning this gene. Methods: 54 patients diagnosed as having PE according to International League Against Epilepsy (ILAE) criteria were included in the study. The patients were analyzed in terms of gender, clinical and syndromic features, response to treatment, EEG features, and photoparoxysmal response (PPR) types. Mutation screening was done by denaturing high-performance liquid chromatography (DHPLC) on all exons belonging to GABRA1 gene. Results: We could not detect any mutation in GABRA1 gene in patients with PE. Four single-nucleotide polymorphisms (SNPs) in GABRA1 gene were observed, but none of them were associated with amino acid changes. Besides, when comparing the patients having these SNPs with the remaining patients without any SNPs in regard to clinical and EEG features, we were not able to find a statistically significant difference for GABRA1 gene. Conclusion: The lack of mutations in the GABRA1 gene indicates that this gene is not predominantly involved in the etiopathogenesis of PE in the Turkish population. In order to get more precise evidence, the research should be extended by increasing the number of patients and by investigating other genes related to GABA. (Archives of Neuropsychiatry 2011; 48: 39-43)
{"title":"Investigation of the Relationship Between Clinical and EEG Findings of Photosensitive Epilepsy and GABA Receptor Alpha 1 Subunit (GABRA1) Gene Mutations","authors":"E. Yavuz, A. Demirkan, Sanne Moen, Ö. Özdemir, Suzin Çatal, N. Bebek, U. Ozbek, B. Baykan","doi":"10.4274/NPA.Y5599","DOIUrl":"https://doi.org/10.4274/NPA.Y5599","url":null,"abstract":"Objective: Although photosensitive epilepsy (PE) is commonly observed, its pathophysiology has not been clarified yet. However, relevant literature indicates that genetic factors play an important role. Our aim was to investigate whether there is a relationship between the clinical and electroencephalographic (EEG) features and the possible mutations/polymorphisms in the GABA receptor alpha 1 subunit (GABRA1) gene in patients with PE by scanning this gene. Methods: 54 patients diagnosed as having PE according to International League Against Epilepsy (ILAE) criteria were included in the study. The patients were analyzed in terms of gender, clinical and syndromic features, response to treatment, EEG features, and photoparoxysmal response (PPR) types. Mutation screening was done by denaturing high-performance liquid chromatography (DHPLC) on all exons belonging to GABRA1 gene. Results: We could not detect any mutation in GABRA1 gene in patients with PE. Four single-nucleotide polymorphisms (SNPs) in GABRA1 gene were observed, but none of them were associated with amino acid changes. Besides, when comparing the patients having these SNPs with the remaining patients without any SNPs in regard to clinical and EEG features, we were not able to find a statistically significant difference for GABRA1 gene. Conclusion: The lack of mutations in the GABRA1 gene indicates that this gene is not predominantly involved in the etiopathogenesis of PE in the Turkish population. In order to get more precise evidence, the research should be extended by increasing the number of patients and by investigating other genes related to GABA. (Archives of Neuropsychiatry 2011; 48: 39-43)","PeriodicalId":51142,"journal":{"name":"Noropsikiyatri Arsivi-Archives of Neuropsychiatry","volume":"1 1","pages":"39-43"},"PeriodicalIF":1.1,"publicationDate":"2011-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4274/NPA.Y5599","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72521979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：