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doc. MUDr. Filip Fencl Ph.D.
Academic staff at Second Faculty of Medicine
2 classes
70 publications
Classes
class
Introduction to Clinical Medicine
D29020009 |
Second Faculty of Medicine
class
Nutrition of child and dietetics
D2904009 |
Second Faculty of Medicine
Publications
publication
COVID-19-associated multisystem inflammatory response syndrome in children. Recommended procedure of the Czech Pediatric Society ČLS JEP
2021 |
Second Faculty of Medicine
publication
Blood pressure in children with renal cysts and diabetes syndrome
2021 |
Second Faculty of Medicine
publication
Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement
2019 |
First Faculty of Medicine, Second Faculty of Medicine
publication
For Debate: The Significance of Etiologic Diagnosis in Neonates with Overgrowth Syndromes. Lesson Learned from the Simpson-Golabi-Behmel Syndrome
2018 |
Second Faculty of Medicine, Central Library of Charles University
publication
Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study
2018 |
Second Faculty of Medicine
publication
Intestinal failure and small intestine transplantation
2017 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
publication
Paediatric Home Parenteral Nutrition in the Czech Republic and Its Development: Multicentre Retrospective Study 1995-2011
2017 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Recurrence of nephrotic proteinuria in children with focal segmental glomerulosclerosis: Early treatment with plasmapheresis and immunoadsorption should be associated with better prognosis
2016 |
Second Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene
2013 |
Second Faculty of Medicine
publication
Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome
2012 |
Second Faculty of Medicine
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