Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sukriye Akca Kalem"'
Autor:
Okan Dogu, Hasmet Hanagasi, Sukriye Akca Kalem, Gulshan Yunisova, Başar Bilgiç, Hakan Gurvit, Zeynep Tufekcioglu, Ebba Lohmann, Hakan Kaleagasi, Murat Emre
Objectives: Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive inborn lipid storage disorder due to various pathogenic mutations in the CYP27A1 gene. Although the symptoms begin commonly in infancy, CTX diagnosis is often delayed. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34d0466cfcb7c681e1a2943163b198ef
https://aperta.ulakbim.gov.tr/record/3107
https://aperta.ulakbim.gov.tr/record/3107
Publikováno v:
Clinical Neurophysiology. 128:579-588
Objective We investigated whether professional air diving with no decompression illness causes any long-term changes in cognitive functions. Methods The all-male participants consisted of 18 healthy control (HC) volunteers and 32 divers. Divers were
Publikováno v:
Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology. 32(2)
Capgras syndrome (CS), also called imposter syndrome, is a rare psychiatric condition that is characterized by the delusion that a family relative or close friend has been replaced by an identical imposter. Here, we describe a 69-year-old man with CS
Autor:
Betül Baykan, Sukriye Akca Kalem, Zuhal Yapici, Sema Saltik, Aysin Dervent, Oget Oktem, Ahmet Gökçay, Ayse Deniz Elmali, Veysi Demirbilek
Saltik, Sema/0000-0002-6749-5795; Elmali, Ayse Deniz/0000-0001-6380-9550
WOS: 000580869300017
PubMed: 31398558
Background: Although the courses of self-limited focal epilepsies of childhood are considered as benign, a handful of studie
WOS: 000580869300017
PubMed: 31398558
Background: Although the courses of self-limited focal epilepsies of childhood are considered as benign, a handful of studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef5faab2a1e2a7d0c6b867936503466b
https://hdl.handle.net/11454/63392
https://hdl.handle.net/11454/63392
Autor:
Sukriye Akca Kalem, Guher Saruhan Direskeneli, Elif Alkaş, Erhan Ertekin, Bengi Baran, Raşit Tükel, Banu Aslantaş Ertekin, Hakan Gurvit
Publikováno v:
The Clinical Neuropsychologist. 30:536-546
In the present study, we investigate the association between the 5-HTTLPR polymorphism and executive functions in a sample of patients with obsessive compulsive disorder (OCD).A total of 98 unmedicated patients diagnosed with OCD according to DSM-IV
Autor:
Ilhan Satman, Sibel Cakir, Birsu Beser, Nevin Dinccag, Sukriye Akca Kalem, Seher Tanrikulu, Cemile Idiz, Gulin Alkan
Publikováno v:
Endocrine Abstracts.
Autor:
Raşit Tükel, Hakan Gurvit, Banu Aslantaş Ertekin, Erhan Ertekin, Berna Özata, Nalan Öztürk, Bengi Baran, Sukriye Akca Kalem, Deniz Büyükgök, Guher Saruhan Direskeneli
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. (7)
In the present study, we have tested the hypothesis that brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism is associated with obsessive–compulsive disorder (OCD) and also investigated the association between the BDNF Val66Met poly
Autor:
Hakan Gurvit, Sukriye Akca Kalem, Ebru Mihci, Sinem Yildiz, Ayfer Tumac, Pinar Unsalan, Başar Bilgiç, Oget Oktem Tanor, Hale Alpaslan
Publikováno v:
Alzheimer's & Dementia. 7
Autor:
Banu Aslantaş Ertekin, Erhan Ertekin, Hakan Gurvit, Raşit Tükel, Bengi Baran, Pınar Elif Kandemir, Sukriye Akca Kalem, Serap Oflaz, Filiz Ozdemiroglu, Figen Atalay
Publikováno v:
Comprehensive Psychiatry, Vol 53, Iss 2, Pp 167-175 (2012)
Obsessive-compulsive disorder (OCD) is a chronic disease characterized by repetitive, unwanted intrusive thoughts and ritualistic behaviors. Studies of neuropsychological functions in OCD have documented deficits in several cognitive domains, particu