Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

…, V Belcastro, A Bianchi, D Yalçın… - The Lancet …, 2018 - thelancet.com
Background Genetic generalised epilepsy is the most common type of inherited epilepsy.
Despite a high concordance rate of 80% in monozygotic twins, the genetic background is still …

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16. 1, 2q22. 3 and 17q21. 32

…, H Caglayan, Z Yapici, DA Yalcin… - Human molecular …, 2012 - academic.oup.com
Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% and account for
20–30% of all epilepsies. Despite their high heritability of 80%, the genetic factors …

Increased erythrocyte susceptibility to lipid peroxidation in human Parkinson's disease

A Kilinç, AS Yalçin, D Yalçin, Y Taga, K Emerk - Neuroscience letters, 1988 - Elsevier
Recent evidence suggests that among the factors that lead to neurodegenerative changes
in Parkinson's disease are stimulation of lipid peroxidation and deficiency of glutathione and …

Hot water epilepsy with cerebral lesion: a report of five cases with cranial MRI findings

FI Tezer, N Ertas, D Yalcin, S Saygi - Epilepsy & Behavior, 2006 - Elsevier
Hot water epilepsy (HWE) is included in the reflex epilepsies. Although, in general, not
common, HWE is concentrated in certain regions of the world. Different bathing habits and …

Evidence against association between arachnoid cysts and epilepsy

AD Yalçın, Ç Öncel, A Kaymaz, N Kuloğlu, H Forta - Epilepsy research, 2002 - Elsevier
Arachnoid cysts are often discovered incidentally in MRs performed for a variety of reasons.
In this study, we have attempted to determine a possible relationship between the arachnoid …

Acquired hepatocerebral degeneration

D Yalçın, E Oğuz-Akarsu, M Sökmen - Neurosciences Journal, 2016 - nsj.org.sa
Acquired hepatocerebral degeneration is a rare, mostly irreversible neurological syndrome
that occurs in patients with chronic liver disease, particularly in those with surgically or …

[HTML][HTML] Overlap cases of eyelid myoclonia with absences and juvenile myoclonic epilepsy

AD Yalçın, H Forta, E Kılıç - Seizure, 2006 - Elsevier
Eyelid myoclonia with absences (EMA) and juvenile myoclonic epilepsy (JME) are two
separate epileptic syndromes included in the new classification of epilepsies and epileptic …

The p. Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN

…, R Sürmeli, G Sünter, T Doğan, AD Yalçın… - Parkinsonism & related …, 2017 - Elsevier
Introduction Mutations in the C19orf12 gene cause mitochondrial membrane protein associated
neurodegeneration (MPAN), an autosomal recessive form of neurodegeneration with …

Hot water epilepsy: clinical and electroencephalographic features of 25 cases

AD Yalçın, HE Toydemir, H Forta - Epilepsy & Behavior, 2006 - Elsevier
The aim of this study was to analyze the clinical and electroencephalographic findings for
25 patients with hot water epilepsy. Personal and family history, neurological state, age at …

Reflex occipital lobe epilepsy

AD Yalçin, A Kaymaz, H Forta - Seizure, 2000 - Elsevier
Photosensitivity is a typical feature of photosensitive epilepsy which is usually considered a
form of idiopathic generalized epilepsy. Partial seizures featuring visual symptoms are rarely …