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Toplam kayıt 9, listelenen: 1-9
Morphological changes in eeg, aquaporin-4, c-fos and the hıppocampus of animal models with temporal lobe epilepsy induced by kainic acid
(Wiley-Blackwell, 2015)
Purpose: Temporal lobe epilepsy (TLE) is the most frequent type of localization relatedfocalepilepsyseeninhumans.Ithasafrequencyrate of 30–35% among all epilepsies, and comprises 70% of intractable epilepsies. With hippocampal ...
Evaluation of suicide probability in children and adolescents with epilepsy
(Wiley, 2022)
Background We aimed to examine suicide probability, factors affecting suicide, and personality traits of children and adolescents diagnosed with epilepsy, and to compare their results with those of children without epilepsy. ...
Çocukluk çağı epilepsilerinde cerrahi tedavi ilkeleri: Pediatrik epilepside ilaca dirençlilik, potansiyel cerrahi tedavi adaylarının belirlenmesi ve bunun için kullanılan ileri teknikler
(Kare Yayıncılık, 2014)
Çocukluk yaş grubunda dirençli epilepsi tedavisinde erken cerrahi tedavi gelişimi olumlu yönde etkiler. Çocuklarda epilepsi sendromlarının büyük kısmını ekstra-temporal loblardan kaynaklanan ve genellikle gelişimsel ...
Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings
(Elsevier B.V., 2022)
Neurexins (NRXNs) are cell-adhesion molecules that play critical roles in establishing and maintaining synaptic connections. Humans have three NRXN genes (NRXN1, NRXN2, NRXN3) and heterozygous intragenic microdeletions ...
HMG-CoA reductase inhibitor rosuvastatin improves abnormal brain electrical activity via mechanisms involving eNOS
(Elsevier, 2015)
Apart from its repressing effect on plasma lipid levels, 3-hydroxy-3-methyl glutaryl coenzyme A (HMG-CoA) reductase inhibitors exert neuroprotective functions in animal models of neurodegenerative disorders. In view of ...
Focal cortical dysplasia: Etiology, epileptogenesis, classification, clinical presentation, imaging, and management
(Springer, 2020)
Background Focal cortical dysplasia (FCD) is the most prevalent cause of intractable epilepsy in children. It was first described by Taylor et al. in 1971. In 2011, the International League against Epilepsy described an ...
Epileptic qualia and self-awareness: A third dimension for consciousness
(Elsevier, 2014)
Over the last few decades, there has been increasing awareness among epileptologists about the need to refine our understanding and assessment of ictal consciousness, focusing on both subjective and behavioral aspects of ...
The impact of epilepsy on preschool children and their families
(Academic Press Inc Elsevier Science, 2016)
This study investigated the possible presence of sensory-motor developmental impairments in preschool children with epilepsy and explored epilepsy impact on their activities and quality of life and on the stress load of ...
The savant syndrome: a gift or a disability? A deeper look into metabolic correlates of hidden cognitive capacity
(Bentham Science Publishers, 2023)
Savant syndrome is a rare and unusual condition that occurs in the presence of severe developmental disabilities, disorders, and injuries. The syndrome can be congenital from birth to childhood or acquired as a result of ...