Language: Bulgarian English

September 10 (Sunday)

Last updated on August 30, 2017

9.00 - 10.30 SESSION 6-I
Moderators: Albena Todorova, Dimitrina Konstantinova
Moderators: Karin Writzl, Olga Boyanova
Ivaylo Tournev Neuromuscular disorders in Roma (Gypsies) Sena Karachanak-Yankova Genome structure of modern Bulgarians
Robert Penchovsky Engineering integrated digital circuits with allosteric ribozymes for scaling up molecular computation and diagnostics of rare diseases Mariya Petrova Medical legal challenges in genetic research
Oral presentations: Ana Pejcic Orphan drugs in Serbia: evaluation of market authorization, pricing, reimbursement and expenditure
Katya Kovacheva Pleven registry of congenital anomalies in the EUROCAT network Oral presentations:
Sara Radunovic Genetic study of achondroplasia in Serbian population Borislav Popov Genetic testing and insurance
Hristo Ivanov Dysregulated pathways in autism spectrum disorder Veselina Petrova-Tacheva Genetic research, family and family relations
Angelina Mandadzhieva Genetically proven cases of Wolman disease in Bulgaria and mutation screening of two presumable endemic regions Rada Staneva The era of precision medicine – a basic guide of how to navigate the field
Marija Brankovic NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C
10.30 - 11.00 Coffee break
11.00 - 12.30 SESSION 7-I
Moderators: Dijana Plaseska Karanfilska, Ugur Ozbek
Moderators: Ivaylo Tournev, Radostina Simeonova
Gueorgui Balatzenko Monitoring of molecular response during the therapy with nilotinib as first-line tyrosine kinase inhibitor in patients with chronic myeloid leukemia Oral presentations:
Oral presentations: Teodora Chamova Autosomal recessive neurologic disorders among Bulgarian Muslims
Zora Hammoudeh Pharmacogenetic studies in patients with cancer Sashka Zhelyazkova Clinical and genetic study of Huntington’s disease: the 9 years of experience of our team
Olga Antonova Screening for SNPs in a set of drug-metabolizing enzymes in Bulgarian population Stayko Sarafov Genetic forms of amyotrophic lateral sclerosis in Bulgaria
Marica Pavkovic Association of Fc gamma receptor polymorphisms with autoimmune hemolytic anaemia Kristina Kastreva Charcot-Marie-Tooth: ethnic differences, genetic and clinical spectrum in Bulgaria
Marija Dusanovic Pjevic Analysis of the association between PAI-1 gene 4G/5G polymorphism and efficacy of thrombolytic therapy in patients with ischemic stroke Jean Samuel The genetic epidemiology of hereditary spastic paraplegias in Bulgaria
Milka Grk Association of ADORA2A gene rs2298383 polymorphism with efficacy/toxicity of MTX Tihomir Todorov NGS approach in cases with congenital neuromuscular disorders
Suada Mucaj Identification of CYP2C19*2 allelic variant in healthy Albanian population Darina Kachakova NGS sequencing in service of neurogenetics in Bulgaria
12.30 - 13.30 Lunch break
13.30 - 14.30 POSTER SESSION 2
Poster jury: Dijana Plaseska Karanfilska, Borut Peterlin, Savina Hadjidekova
14.30 - 16.00 SESSION 8-I
Moderators: Katya Kovacheva, Borislav Popov
Moderators: Lyudmila Angelova, Trifon Chervenkov
Oral presentations: Oral presentations:
Slavica Josifovska Genetic heterogeneity of cardio vascular diseases associated with pathology of great vessels Zoran Gucev Rare Diseases, new genes, molecular mechanisms and treatments
Mariana Gospodinova Genetics and cardio-vascular diseases Ana Marjanovic Study of ATXN2 repeat length in C9ORF72 expansion
Elena Sukarova Angelovska Recognition of syndromic forms of disorders of sexual differentiation Grigor Zoraqi Spectrum of mutations in the CFTR gene of Albanian cystic fibrosis patients
Valentin Penchev Genetic background of steroid-resistant nephrotic syndrome in Bulgaria Mariya Glushkova Genetically verified tuberous sclerosis complex in a cohort of fifteen Bulgarian families
Olga Beltcheva Molecular basis of developmental disorders: a view through the kidney filter Dragomira Nikolova Molecular profiling of papillary thyroid cancer by RNA expression and NGS sequencing platforms
Mila Baycheva Diagnostic and therapeutic approach in children with biliary atresia Silva Giragosyan Genetic profiling of advanced laryngeal carcinoma by NGS
16.00 - 17.00 CLOSING SESSION
Moderators: Draga Toncheva, Rumen Stefanov

Please, note that the programme is subject to change and will be updated continuously up to the Congress. Visit the Congress website regularly to stay informed.


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