Characteristics of isolated spinal cord involvement in neurobrucellosis with no corresponding MRI activity: A case report and review of the literature
T Gündüz, PT Tektürk, Z Yapıcı, M Kürtüncü… - Journal of the …, 2017 - jns-journal.com
2. Discussion Although rare, neurobrucellosis is still an important problem throughout the
world. At any stage of systemic brucellosis, neurologic involvement (neurobrucellosis [NB]) …
world. At any stage of systemic brucellosis, neurologic involvement (neurobrucellosis [NB]) …
The complex genetic landscape of hereditary ataxias in Turkey and implications in clinical practice
Background The genetic and epidemiological features of hereditary ataxias have been
reported in several populations; however, Turkey is still unexplored. Due to high …
reported in several populations; however, Turkey is still unexplored. Due to high …
Investigation of neuronal auto-antibodies in systemic lupus erythematosus patients with epilepsy
Z Karaaslan, E Ekizoğlu, P Tektürk, E Erdağ, E Tüzün… - Epilepsy Research, 2017 - Elsevier
Purpose Epilepsy is an important feature for neuropsychiatric involvement in systemic lupus
erythematosus (SLE) with unknown mechanism. Our aim was to investigate the presence of …
erythematosus (SLE) with unknown mechanism. Our aim was to investigate the presence of …
Kv5. 1 antibody in epilepsy patients with unknown etiology
Background Neuronal autoantibodies and favorable response to immunosuppressive
treatment have been described in patients with chronic epilepsy of unknown cause …
treatment have been described in patients with chronic epilepsy of unknown cause …
Neuronal autoantibodies in patients with Rasmussen's encephalitis
B Samanci, P Tektürk, E Tüzün, E Erdağ… - Epileptic …, 2016 - Wiley Online Library
Aim. Rasmussen's encephalitis (RE) is a rare disease with unknown pathophysiology. To
disclose whether anti‐neuronal autoimmunity participates in the aetiology of RE, various …
disclose whether anti‐neuronal autoimmunity participates in the aetiology of RE, various …
A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy
NH Akçakaya, Z Yapıcı, Cİ Tunca, P Tektürk… - Journal of Neurology …, 2018 - jnnp.bmj.com
Solute carrier family 12 member 6 (SLC12A6) mutations have been found to be responsible
for the phenotype that causes agenesis of the corpus callosum (CC) with peripheral …
for the phenotype that causes agenesis of the corpus callosum (CC) with peripheral …
Calcium channel antibodies in patients with absence epilepsy
Autoimmunity has aroused interest in the last years as a contributory mechanism of epilepsy,
especially in epilepsies with unknown cause or therapy resistance. Since the relationship of …
especially in epilepsies with unknown cause or therapy resistance. Since the relationship of …
[HTML][HTML] Galactosemia and phantom absence seizures
Z Aydin-Özemir, P Tektürk, ZO Uyguner… - Journal of Pediatric …, 2014 - journals.lww.com
Generalized and focal seizures can rarely be seen in galactosemia patients, but absence
seizures were not reported previously. An 18-year-old male was diagnosed as galactosemia …
seizures were not reported previously. An 18-year-old male was diagnosed as galactosemia …
[HTML][HTML] SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations
Abstract Purpose The SCN1A gene is one of the most commonly mutated human epilepsy
genes associated with a spectrum of phenotypes with variable degrees of severity. Despite …
genes associated with a spectrum of phenotypes with variable degrees of severity. Despite …
Febrile Infection Related Epilepsy Syndrome (FIRES) in Adults Imitating Limbic Encephalitis.
P TEKTÜRK, B Baykan… - Journal of Neurological …, 2015 - search.ebscohost.com
Febrile infection-related epilepsy syndrome (FIRES) is a rare but devastating condition of the
children and only a few adults with similar clinical conditions have been reported so far. Two …
children and only a few adults with similar clinical conditions have been reported so far. Two …