Scientific programme
Friday 17 June 2022 |
|
08.30 - 08.40 |
Opening ceremony |
08.40 - 09.10 |
KEYNOTE LECTURE |
chair: | Petr Jabandziev |
Gregor Mendel celebrates 200 years: from the gardens of the Augustinian monastery in Brno to the treatment of monogenic diseases and precision oncology Ondrej Slaby |
|
09.10 - 11.40 |
PANEL I |
chairs: | Jiri Bronsky, Natasa Marcun Varda |
1. |
Hypersensitivity reactions to beta-lactam antibiotics in children Dvorakova L. et al. |
2. |
TREC analysis of newborns at tertial clinical centre Hulinkova I. et al. |
3. |
Personalized molecularly guided treatment for vascular malformations harboring PIK3CA and TEK mutation in children, adolescents, and young adults: A single-center case series with high response rate and low toxicity profile Sterba M. et al. |
4. |
Bone mineral density and oxidative stress in adolescent girls with anorexia nervosa
Gaal Kovalcikova A. et al. |
5. |
Cross-Sectional Study of the Prevalence of Cobalamin Deficiency and Vitamin B12 Supplementation Habits among Vegetarian and Vegan Children in the Czech Republic Svetnicka M. et al. |
6. |
Effects of anti-TNFα therapy on the faecal bacteriome in paediatric patients with Crohn’s disease in contrast to juvenile idiopathic arthritis – the MICROJATT study Hurych J. et al. |
7. |
Ultrasound elastography of liver and kidneys in children and young adults – a pilot study Mocnik M. et al. |
8. |
Chronic recurrent multifocal osteomyelitis - clinical and genetic features of paediatric patients Pytelova Z. et al. |
9. |
Monitoring of pulmonary functions by lung clearance index using multiple breath washout tests in premature infants with bronchopulmonary dysplasia Cernanova K. et al. |
10. |
Real-life vaccination coverage in children with rheumatic diseases Balaziova B. et al. |
11.40 - 12.30 |
Lunch |
12.30 - 15.00 |
PANEL II |
chairs: | Radvan Urbanek, Tomas Honzik |
11. |
Five Czech patients with mitochondrial aminoacyl-tRNA synthetase deficiencies: mutations, phenotypes, and common findings in these ultra-rare syndromes Hanak P. et al. |
12. |
Cardiac manifestation in patients with PMM2-CDG Holubova V. et al. |
13. |
Czech cohort of patients with subacute visual loss caused by pathogenic variant in DNAJC30 gene Kelifova S. et al. |
14. |
Postvaccination and postinfection COVID-19 response in pediatric primary immunodeficient patients Nabova B. et al. |
15. |
Glycine encephalopathy - Czech Republic cohort Kulhanek J. et al. |
16. |
Transient Agarose Spot (TAS) assay: a new method to investigate cell migration Veres-Szekely A. et al. |
17. |
Multiomic aproach in treatment of refractory/relapsed ependymomas in the era of personalised medicine Tinka P. et al. |
18. |
Characterization of mTOR Activity and Metabolic Profile in Pediatric Rhabdomyosarcoma Felkai L. et al. |
19. |
Three Waves of PIMS-TS Misikova D. et al. |
20. |
Start up of a database of medicines for the paediatric population in the Czech Republic in 2022 Pavlikova S. et al. |
15.00 - 15.30 |
Coffee break |
15.30 - 17.45 |
PANEL III |
chairs: | Ludmila Podracka, Jan Janda |
21. |
PARK7 – a novel therapeutic target for peritoneal dialysis induced peritoneal membrane and vascular transformation Levai E. et al. |
22. |
Acute tubulointerstitial nephritis in children – a retrospective case series in a Czech tertiary pediatric centre Papez J. et al. |
23. |
Novel integrative method to identify therapeutic targets and compounds for treating kidney fibrosis Pap D. et al. |
24. |
Extracellular vesicles from peritoneal dialysate moderated progression of peritoneal dialysis associated peritoneal fibrosis Szebeni B. et al. |
25. |
Autosomal recessive polycystic kidney disease in Slovak and Czech patients Hrckova G. et al. |
26. |
Extracellular DNA is possible early marker of kidney damage Gaal Kovalcikova A. et al. |
27. |
Distribution of paediatric diabetes subtypes in a consanguineous region: a single center study Amaratunga S.A. et al. |
28. |
Genetic analysis of children with clinically non-syndromic tall stature Adamovicova K. et al. |
29. |
Growth hormone deficiency: Extending phenotypic spectrum of SALL4 related disorders Kodytkova A. et al. |
17.50 - 18.30 |
POSTER SESSION |
chair: | Jan Lebl |
P01. |
Patients with congenital anomalies of kidney and urinary tract (cakut) share common hotspot loci with low frequency variants Zapusek J. et al. |
P02. |
Non-invasive assessment of vascular system function and damage induced by anthracycline treatment in the pediatric cancer survivors Pirek O. et al. |
P03. |
Using multimodal monitoring on neonates undergoing anesthesia for surgery Trinh S. et al. |
P04. |
Deep venous thrombosis in children with malignant diseases Despotovic M. et al. |
P05. |
Infections in children with acute lymphoblastic leukemia Vraneševic K. et al. |
P06. |
Neutropenia in children: A single-center experience Zubovic M. et al. |
P07. |
Thalassemia in children: a single center experience Đorđevic A. et al. |
P08. |
Prediction of effect of nutritional induction therapy in newly diagnosed paediatric patients with luminal Crohn’s disease using metabolomic profiling: preliminary data Kubat M. et al. |
P09. |
Monitoring the use of medicinal products in the pediatric population and safety parameters in a single center Slezakova M. et al. |
P10. |
Case report PSC-IBD Vlčková E. |
18.45 - 20.00 |
Visit to the Simulation Centre of the Faculty of Medicine, Masaryk University |
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The programme is subject to change.