Serhat Güler

Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy

Cas Simons, Lachlan D. Rash, Joanna Crawford et al. · Nature Genetics · 2014 · 156 citations

Channelopathies, Hyperpolarization (Biology), Neurophysiology +8

Evaluation of malnutrition development risk in hospitalized children

Ömer Faruk Beșer, Fügen Çokuğraş, Tülay Erkan et al. · Nutrition · 2017 · 128 citations · Full text

Relationship between the corpus callosum and neurocognitive disabilities in children with NF-1: diffusion tensor imaging features

Serpil Kurtcan, Alpay Alkan, Serhat Güler et al. · Clinical Imaging · 2016 · 35 citations

Neurodevelopmental Disorders, Neuroimaging Modality, Brain Structure +12

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals

Ken Saida, Reza Maroofian, Toru Sengoku et al. · Genetics in Medicine · 2022 · 34 citations

Neurodegenerative Diseases, Psychiatry, Homozygous Slc18a2 Variants +8

Prognosis and demographic characteristics of SSPE patients in Istanbul, Turkey

Serhat Güler, Mehmet Küçükkoç, Akın İşcan · Brain and Development · 2014 · 30 citations

Clinical Epidemiology, Diagnosis, Sspe Patients +3