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Frontiers in Psychiatry|November 7, 2022
Re-emerging concepts of immune dysregulation in autism spectrum disordersAlina Erbescu, Sorina Mihaela Papuc, Magdalena Budisteanu, et al.Italian Journal of Pediatrics|September 28, 2024
A rare cause of epileptic encephalopathy: case report of a novel patient with PEHO-like phenotype and CCDC88A gene pathogenic variantsSorina-Mihaela Papuc, Adelina Glangher, Alina Erbescu, et al.Genes|February 25, 2023
Autistic Behavior as Novel Clinical Finding in OFD1 SyndromeSorina Mihaela Papuc, Alina Erbescu, Adelina Glangher, et al.Open Life Sciences|May 14, 2021
Treatment of Epilepsy Associated with Common Chromosomal Developmental DiseasesMagdalena Budisteanu, Claudia Jurca, Sorina Mihaela Papuc, et al.Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie|October 29, 2019
Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literatureMagdalena Budişteanu, Carmen Magdalena Burloiu, Sorina Mihaela Papuc, et al.Reviews in the Neurosciences|November 20, 2024
Review of structural neuroimaging and genetic findings in autism spectrum disorder - a clinical perspectiveMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.Journal of Child Neurology|February 1, 2012
3p interstitial deletion: novel case report and reviewAndreea Cristina Ţuţulan-Cunită, Sorina Mihaela Papuc, Aurora Arghir, et al.Psychiatry Research|February 28, 2012
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureAndreea Cristina Tuţulan-Cuniţă, Magdalena Budişteanu, Sorina Mihaela Papuc, et al.Plos One|May 3, 2017
Plasma metabolomics reveals a diagnostic metabolic fingerprint for mitochondrial aconitase (ACO2) deficiencyLucia Abela, Ronen Spiegel, Lisa M Crowther, et al.Diagnostics (Basel, Switzerland)|June 12, 2026
Understanding the Complexity of Sleep Disturbances in ASD: From Mechanisms to ManagementAdelina Glangher, Ina-Ofelia Focsa, Vanda Roxana Nimigean, et al.Pageof 3