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Arii de interes: Genetica medicala: tehnici de genetica moleculara pentru diagnosticul bolilor genetice; consult/consiliere geneticaBoli de neurodezvoltare si neurodegenerativeBoli congenitale de metabolismBoli mitocondrialeFarmacogeneticaCursuri postuniversitare: 2013: Dysmorphology Course, ESHG, Manchester, Marea Britanie2013: Al 7-lea curs Roman-German de Genetica medicala, Oradea 2012: Chromosomal disorders, UCLA Medical Center, Department of Pathology and laboratory Medicine 2012: Molecular Pathobiology Short Course, Cluj-Napoca (20.04.2012)2011: Curs de Citogenetica moleculara, Institutul National de Cercetare-Dezvoltare V. Babes, Bucuresti 2010: Abordarea interdisciplinara a bolilor genetice rare, UMF Timisoara & Societatea Romana de Genetica medicala 2006: Impactul geneticii in patologia umana, UMF Cluj-Napoca & Societatea Romana de Genetica medicala 2005: Al 4-lea curs Germano-Roman de Genetica medicala, UMF Oradea & Societatea Romana de Genetica medicala & Universitatile din Minz, Essen si Wurzburg, Germania & Nijmegen, Olanda & UMF Iasi2004: Biotehnologii moleculare – aplicatii medicale, Catedra de Biochimie, UMF Cluj-Napoca Publicatii: Genotype-phenotype Analysis of Paraoxonase 1 in Schizophrenic Patients Treated with Atypical Antipsychotics, Clin Psychopharmacol Neurosci 16(1):32-38Low Retinal Dehydrogenase 1 (RALDH1) Level in Prepubertal Boys with Autism Spectrum Disorder: A Possible Link to Dopamine Dysfunction? Clin Psychopharmacol Neurosci 15(3):229-236Evaluation of whole blood zinc and copper levels in children with autism spectrum disorder, Metab Brain Dis 31:887-890 Paraoxonase-1 activities in children and adolescents with type 1 diabetes mellitus, Acta Biochimica Polonica 63(3):511-515Low Serum Paraoxonase-1 Lactonase and Arylesterase Activities in Obese Children and Adolescents, Revista Romana de Medicina de Laborator 23(4):385-396 Paraoxonase 1 genotype-phenotype correlation in patients with metabolic syndrome, Rom J Morphol Embryol 56(2):387-392High levels of homocysteine and low serum paraoxonase 1 arylesterase activity in children with autism, Life Sciences 78(19):2244-2248One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders, Journal of Cellular and Molecular Medicine 13(10):4229-4238  Paraoxonase 1 activities and polymorphisms in autism spectrum disorders, Journal of Cellular and Molecular Medicine 14(3):600-607 Distribution of Paraoxonase 1 polymorphisms and activities in obese patients, Rev Romana Med Lab 21(4):381-389 Antioxidant enzymes activity in subjects with Parkinson’s disease under L-DOPA therapy, Human and Veterinary Medicine 8(2):124-127  Cytogenetic and fragile X testing in a group of Romanian autistic children, Human and Veterinary Medicine 7(4):276-282 Statusul PON1 in schizofrenie, Clujul Medical LXXX(2):336-341 ISSN 1222-2119 Paraoxonase (PON1) polymorphisms in autism, Annals of West University of Timisoara Series of Chemistry 16(2):163-168 Correlation between several extrinsic factors and Paraoxonase 1 activities, Human and Veterinary Medicine 5(3):88-93 Investigation of the paraoxonase 1 (PON1) promoter polymorphism C(-108)T and activities in autism spectrum disorders, Rom J Biochem 46(1):13–23 Sindroame genetice in autism, Maramuresul medical XV(53):70-74Membru in: Societatea Romana de Genetica Medicala (SRGM)Societatea Europeana de Genetica Medicala (ESHG)Societatea Romana de Neurostiinte (SRN)Societatea Romana de Morfologie (SRM)