Odborný program
Pátek 17. 6. 2022 |
|
08.30 - 08.40 |
Slavnostní zahájení |
08.40 - 09.10 |
HLAVNÍ PŘEDNÁŠKA |
| předsedající: | Petr Jabandžiev |
| Gregor Mendel celebrates 200 years: from the gardens of the Augustinian monastery in Brno to the treatment of monogenic diseases and precision oncology Slabý Ondřej |
|
09.10 - 11.40 |
PANEL I |
| předsedající: | Jiří Bronský, Nataša Marčun Varda |
| 1. |
Hypersensitivity reactions to beta-lactam antibiotics in children Dvořáková L. a kolektiv |
| 2. |
TREC analysis of newborns at tertial clinical centre Hulínková I. a kolektiv |
| 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 Štěrba M. a kolektiv |
| 4. |
Bone mineral density and oxidative stress in adolescent girls with anorexia nervosa
Gaál Kovalčíková A. a kolektiv |
| 5. |
Cross-Sectional Study of the Prevalence of Cobalamin Deficiency and Vitamin B12 Supplementation Habits among Vegetarian and Vegan Children in the Czech Republic Světnička M. a kolektiv |
| 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. a kolektiv |
| 7. |
Ultrasound elastography of liver and kidneys in children and young adults – a pilot study Močnik M. a kolektiv |
| 8. |
Chronic recurrent multifocal osteomyelitis - clinical and genetic features of paediatric patients Pytelová Z. a kolektiv |
| 9. |
Monitoring of pulmonary functions by lung clearance index using multiple breath washout tests in premature infants with bronchopulmonary dysplasia Čerňanová K. a kolektiv |
| 10. |
Real-life vaccination coverage in children with rheumatic diseases Balažiová B. a kolektiv |
11.40 - 12.30 |
Oběd |
12.30 - 15.00 |
PANEL II |
| předsedající: | Radvan Urbanek, Tomáš Honzík |
| 11. |
Five Czech patients with mitochondrial aminoacyl-tRNA synthetase deficiencies: mutations, phenotypes, and common findings in these ultra-rare syndromes Hanák P. a kolektiv |
| 12. |
Cardiac manifestation in patients with PMM2-CDG Holubová V. a kolektiv |
| 13. |
Czech cohort of patients with subacute visual loss caused by pathogenic variant in DNAJC30 gene Kelifová S. a kolektiv |
| 14. |
Postvaccination and postinfection COVID-19 response in pediatric primary immunodeficient patients Nabová B. a kolektiv |
| 15. |
Glycine encephalopathy - Czech Republic cohort Kulhánek J. a kolektiv |
| 16. |
Transient Agarose Spot (TAS) assay: a new method to investigate cell migration Veres-Székely A. a kolektiv |
| 17. |
Multiomic aproach in treatment of refractory/relapsed ependymomas in the era of personalised medicine Tinka P. a kolektiv |
| 18. |
Characterization of mTOR Activity and Metabolic Profile in Pediatric Rhabdomyosarcoma Felkai L. a kolektiv |
| 19. |
Three Waves of PIMS-TS Mišíková D. a kolektiv |
| 20. |
Start up of a database of medicines for the paediatric population in the Czech Republic in 2022 Pavlíková S. a kolektiv |
15.00 - 15.30 |
Coffee break |
15.30 - 17.45 |
PANEL III |
| předsedající: | Ľudmila Podracká, Jan Janda |
| 21. |
PARK7 – a novel therapeutic target for peritoneal dialysis induced peritoneal membrane and vascular transformation Levai E. a kolektiv |
| 22. |
Acute tubulointerstitial nephritis in children – a retrospective case series in a Czech tertiary pediatric centre Papež J. a kolektiv |
| 23. |
Novel integrative method to identify therapeutic targets and compounds for treating kidney fibrosis Pap D. a kolektiv |
| 24. |
Extracellular vesicles from peritoneal dialysate moderated progression of peritoneal dialysis associated peritoneal fibrosis Szebeni B. a kolektiv |
| 25. |
Autosomal recessive polycystic kidney disease in Slovak and Czech patients Hrčková G. a kolektiv |
| 26. |
Extracellular DNA is possible early marker of kidney damage Gaál Kovalčíková A. a kolektiv |
| 27. |
Distribution of paediatric diabetes subtypes in a consanguineous region: a single center study Amaratunga S.A. a kolektiv |
| 28. |
Genetic analysis of children with clinically non-syndromic tall stature Adamovičová K. a kolektiv |
| 29. |
Growth hormone deficiency: Extending phenotypic spectrum of SALL4 related disorders Kodytková A. a kolektiv |
17.50 - 18.30 |
POSTEROVÁ SEKCE |
| předsedající: | Jan Lebl |
| P01. |
Patients with congenital anomalies of kidney and urinary tract (cakut) share common hotspot loci with low frequency variants Zapušek J. a kolektiv |
| P02. |
Non-invasive assessment of vascular system function and damage induced by anthracycline treatment in the pediatric cancer survivors Pírek O. a kolektiv |
| P03. |
Using multimodal monitoring on neonates undergoing anesthesia for surgery Trinh S. a kolektiv |
| P04. |
Deep venous thrombosis in children with malignant diseases Despotović M. a kolektiv |
| P05. |
Infections in children with acute lymphoblastic leukemia Vranešević K. a kolektiv |
| P06. |
Neutropenia in children: A single-center experience Zubović M. a kolektiv |
| P07. |
Thalassemia in children: a single center experience Đorđević A. a kolektiv |
| P08. |
Prediction of effect of nutritional induction therapy in newly diagnosed paediatric patients with luminal Crohn’s disease using metabolomic profiling: preliminary data Kubát M. a kolektiv |
| P09. |
Monitoring the use of medicinal products in the pediatric population and safety parameters in a single center Slezáková M. a kolektiv |
| P10. |
Case report PSC-IBD Vlčková E. |
18.45 - 20.00 |
Návštěva Simulačního centra LF MU |
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Změna programu vyhrazena.