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Transcultural Psychiatry|May 22, 2024
PTSD, depression, and migration-related experiences among Syrian refugees living in camp vs urban settingsEsra Isik, Sahika Gulen Sismanlar, Sidika Tekeli-YesilNeurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2018
WWOX-associated encephalopathies: identification of the phenotypic spectrum and the resulting genotype-phenotype correlationHepsen Mine Serin, Erdem Simsek, Esra Isik, et al.European Journal of Medical Genetics|September 24, 2018
Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotypingEsra Isik, Ayca Aykut, Tahir Atik, et al.Clinical Neurology and Neurosurgery|August 21, 2021
Mutation spectrum of the NF1 gene and genotype-phenotype correlations in Turkish patients: Seventeen novel pathogenic variantsAsli Ece Solmaz, Esra Isik, Tahir Atik, et al.Clinical Neurology and Neurosurgery|July 1, 2018
Clinical and genetic features of L1 syndrome patients: Definition of two novel mutationsEsra Isik, Huseyin Onay, Tahir Atik, et al.European Journal of Medical Genetics|July 19, 2019
Clinical utility of a targeted next generation sequencing panel in severe and pediatric onset Mendelian diseasesEsra Isik, Huseyin Onay, Tahir Atik, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 25, 2020
The utility of whole exome sequencing for identification of the molecular etiology in autosomal recessive developmental and epileptic encephalopathiesEsra Isik, Sanem Yilmaz, Tahir Atik, et al.Annals of Clinical Biochemistry|February 19, 2021
Clinical and molecular findings in children and young adults with persistent low alkaline phosphatase concentrationsMehmet Bilal Araci, Bilcag Akgun, Tahir Atik, et al.Journal of Thrombosis and Haemostasis : JTH|July 6, 2023
A unique case of thrombophilia: the role of F9 gene duplication and increased factor IX activity in cerebral venous thrombosisTurkan Turkut Tan, Erhan Pariltay, Enise Avci Durmusaliogu, et al.Molecular Syndromology|January 29, 2021
Clinical and Molecular Spectrum of Four Patients Diagnosed with Mowat-Wilson SyndromeDurdugul Ayyildiz Emecen, Esra Isik, Gulen E Utine, et al.Pageof 4