Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Berrin Aktekin"'
Publikováno v:
Türk Nöroloji Dergisi, Vol 18, Iss 1, Pp 36-38 (2012)
Noonan syndrome is an autosomal dominant genetic disease characterized by short stature, webbed neck, typical facial appearance and congenital heart disease. Here we report a 24 year old woman patient with the diagnosis of Noonan syndrome who admitte
Externí odkaz:
https://doaj.org/article/3cf06adadaf34ef08c9f3001f4ada9c1
Autor:
Nihal Olgac Dundar, Berrin Aktekin, Nilufer Cicek Ekinci, Duygu Sahinturk, Ugur Yavuzer, Olcay Yegin, Senay Haspolat
Publikováno v:
Neurology International, Vol 5, Iss 3, Pp e17-e17 (2013)
Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE-HS) is a common medically intractable epilepsy syndrome. Although pathogenesis of HS still remains highly controversial, genetics may play a role as a predisposing factor. Previous eviden
Externí odkaz:
https://doaj.org/article/851d016a4aea446ca695e4fa5fdc7c08
Autor:
Nail Demirel, Ceyhun Saymaz, Mustafa Kaya, Hanife Gülden Düzkalir, Berrin Aktekin, Selcuk Ozdogan, Basar Sarikaya, Ali Haluk Duzkalir, Cumhur Kaan Yaltirik
Publikováno v:
The American Journal of Case Reports
WOS: 000417191500001
PubMed: 29192135
Patient: Male, 11 Final Diagnosis: Haberland syndrome Symptoms: Seizure Medication: - Clinical Procedure: Medical treatment Specialty: Neurosurgery Objective: Rare disease Background: Encephalocraniocut
PubMed: 29192135
Patient: Male, 11 Final Diagnosis: Haberland syndrome Symptoms: Seizure Medication: - Clinical Procedure: Medical treatment Specialty: Neurosurgery Objective: Rare disease Background: Encephalocraniocut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec310c3d62ef55143b72c0fe1db22047
https://doi.org/10.12659/ajcr.907685
https://doi.org/10.12659/ajcr.907685
Autor:
Canan Aykut Bingol, Berrin Aktekin, Muzaffer Değertekin, Pınar Bekdik Şirinocak, Basar Sarikaya
Publikováno v:
The Journal of Tepecik Education and Research Hospital.
Sturge-Weber syndrome (SWS) is a rare neurocutaneous disease characterized with a port-wine stain and ipsilateral leptomeningeal angiomas. It may cause wide variety of neurological signs and symptoms.A 63-year-old female patient with a port-wine stai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a4f643e1cf5e7ec796d2b1ee3c5963b
https://doi.org/10.5222/terh.2019.81567
https://doi.org/10.5222/terh.2019.81567
Publikováno v:
SIU
Epilepsy is a chronic neurological disorder in which the normal pattern of neuronal activity in the brain becomes disturbed. Identification of the brain region that is abnormally active during an epileptic seizure is vital for epilepsy surgery. One w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fcf6e3840787f8d3b053a422d1fd108
https://hdl.handle.net/20.500.11831/6999
https://hdl.handle.net/20.500.11831/6999
Autor:
Ebru Barcin, Berrin Aktekin
Publikováno v:
Nöro Psikiyatri Arşivi. :189-194
In the light of the latest knowledge acquired from clinical and laboratory research dealing with genetic, molecular biology and neuroimaging, existing classifications were successively revised by the International League Against Epilepsy (ILAE) in 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b34434285831237152580b8b0dd5cd7
https://doi.org/10.4274/npa.y7062
https://doi.org/10.4274/npa.y7062
Autor:
Berrin Aktekin
Publikováno v:
Journal of the Turkish Epilepsi Society.
Epilepsi poliklinikleri, epilepsili bireylerin rutin tedavilerinin yani sira nobetleri kontrol edilemeyenlerin genis kapsamli tani ve tedavilerinin yapilabildigi, epilepsi ile yakindan ilgili noroloji uzmanlarinin gorev yaptigi ve multidisipliner yak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ea331483a081a9c8236fa44c4bcfe0f
https://doi.org/10.5505/epilepsi.2012.28290
https://doi.org/10.5505/epilepsi.2012.28290
Autor:
Ugur Bilge, S Akdeniz, Ö Duman, Berrin Aktekin, Nihal Olgaç Dündar, Guven Luleci, Deniz Ozel, Senay Haspolat, Esra Manguoğlu
Publikováno v:
Balkan Journal of Medical Genetics, Vol 14, Iss 1, Pp 25-30 (2011)
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics : BJMG
RLIP76Gene Variants are not Associated with Drug Response in Turkish Epilepsy PatientsApproximately 30% of epileptic patients remain untreated, in spite of trials with maximum tolerable doses of more than one drug. The RalA binding protein 1 (RALBP1/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66abc45033a2224751cf4549d26a2e49
https://doi.org/10.2478/v10034-011-0014-3
https://doi.org/10.2478/v10034-011-0014-3
Publikováno v:
Epilepsy & Behavior. 13:156-161
The aim of the study described here was to investigate the efficacy, tolerability, and side effects of oxcarbazepine (OXC) monotherapy in newly diagnosed, previously untreated adult and elderly patients with partial epilepsy.We prospectively analyzed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474590f384ba38346f85a139db7306d2
https://doi.org/10.1016/j.yebeh.2008.02.001
https://doi.org/10.1016/j.yebeh.2008.02.001
Publikováno v:
Clinical Neurology and Neurosurgery. 108:392-395
Behçet's disease (BD) is a multisystemic, recurrent, inflammatory disorder of unknown aetiology. Neurological involvement is characterised either by primary parenchymal lesions or secondary to major vascular involvement. Seizures are rarely seen in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af0b68dc5312c2c419f795df121e3093
https://doi.org/10.1016/j.clineuro.2004.12.021
https://doi.org/10.1016/j.clineuro.2004.12.021