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The Journal of Obstetrics and Gynaecology Research|January 3, 2013
Cord blood ischemia-modified albumin: is it associated with abnormal Doppler findings in complicated pregnancies and predictive of perinatal asphyxia?Abdullah Kumral, Emre Okyay, Serkan Guclu, et al.
Frontiers in Public Health|February 6, 2025
Management of rare and undiagnosed diseases: insights from researchers and healthcare professionals in TürkiyeSinem Durmus, Emrah Yucesan, Sinem Aktug, et al.
Frontiers in Neurology|March 16, 2026
Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approachesAyca Yigit, Ozlem Akgun-Dogan, Zeynep Ozkeserli, et al.
Neurogenetics|February 14, 2022
Experiences in the molecular genetic and histopathological evaluation of calpainopathiesBerk Ozyilmaz, Ozgur Kirbiyik, Taha R Ozdemir, et al.
European Journal of Pediatrics|March 20, 2025
Phenotypic variability in cases with CACNA1A mutationSema Bozkaya-Yilmaz, Nihal Olgac-Dundar, Nargiz Aliyeva, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 29, 2021
Evaluation of micronutrient levels in children with cerebral palsyKursat Bora Carman, Kursad Aydın, Betul Kilic Aydin, et al.
European Journal of Pediatrics|August 6, 2021
Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC studySema Bozkaya-Yilmaz, Eda Karadag-Oncel, Nihal Olgac-Dundar, et al.
Epilepsy & Behavior : E&B|March 24, 2026
The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort studyPinar Ozkan Kart, Esra Serdaroglu, Nihal Yildiz, et al.
Open Research Europe|January 22, 2026
Collaborative development of a scoping review protocol to map instruments assessing the parent-infant relationship: An International Initiative from COST Action TREASURESónia Brandão, Anat Talmon, Ewa Gieysztor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2024
Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disordersElisa Cali, Tania Quirin, Clarissa Rocca, et al.
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