Bilge Volkan Salancı

A Homozygous Deletion in <i>GRID2</i> Causes a Human Phenotype With Cerebellar Ataxia and Atrophy

Gülen Eda Ütine, Göknur Haliloğlu, Bilge Volkan Salancı et al. · Journal of Child Neurology · 2013 · 72 citations

Neurological Disorder, Genetics, Synaptic Signaling +20

The effect of clozapine on regional cerebral blood flow and brain metabolite ratios in schizophrenia: Relationship with treatment response

Aygün Ertuğrul, Bilge Volkan Salancı, Koray Başar et al. · Psychiatry Research Neuroimaging · 2009 · 65 citations

Psychiatry, Psychotic Disorder, Psychotropic Medication +12

SPECT in periodic lateralized epileptiform discharges (PLEDs): A case report on PLEDs

Eser Lay Ergün, Bilge Volkan Salancı, Belkis Erbas · Annals of Nuclear Medicine · 2006 · 42 citations

Case Report

Serum PON-1 Activity but not Q192R Polymorphism is Related to the Extent of Atherosclerosis

Ahmet Bayrak, Tülin Bayrak, S. Lale Tokgözoğlu et al. · Journal of Atherosclerosis and Thrombosis · 2011 · 39 citations · Full text

A multidisciplinary approach to the management of individuals with fragile X syndrome

Yasemin Alanay, Fatih Ünal, Güzide Turanlı et al. · Journal of Intellectual Disability Research · 2007 · 36 citations