Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Filip Fencl

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
European Journal of Pediatrics|November 1, 2015
A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literatureMichaela Nemcikova, Sarka Vejvalkova, Filip Fencl, et al.
European Journal of Pediatrics|September 25, 2012
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 geneFilip Fencl, Květa Bláhová, Karl Peter Schlingmann, et al.
Frontiers in Pediatrics|June 23, 2023
Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature reviewJakub Zieg, Terezia Tavačová, Miroslava Balaščáková, et al.
European Journal of Pediatrics|May 27, 2011
Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndromeFilip Fencl, Michal Malina, Veronika Stará, et al.
Casopis Lekaru Ceskych|October 11, 2017
[Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes]Jan Lebl, Lukáš Plachý, Květa Bláhová, et al.
Pediatric Nephrology (Berlin, Germany)|February 6, 2009
Genotype-phenotype correlation in children with autosomal dominant polycystic kidney diseaseFilip Fencl, Jan Janda, Kveta Bláhová, et al.
European Journal of Pediatrics|September 26, 2018
Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary studyLucia Karnisova, Ondrej Hradsky, Kveta Blahova, et al.
Klinische Padiatrie|July 31, 2025
Reduction of Parenteral Nutrition in Children with Short Bowel Syndrome Treated with Teduglutide: Experience from the Czech RepublicSarka Peskova, Astrida Sulakova, Katerina Bajerova, et al.
Pediatric Nephrology (Berlin, Germany)|December 20, 2022
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertensionTomáš Seeman, Kveta Bláhová, Filip Fencl, et al.
Plos One|June 24, 2020
Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosisLena Obeidova, Tomas Seeman, Filip Fencl, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
European Journal of Pediatrics|November 1, 2015
A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation-a review of the literatureMichaela Nemcikova, Sarka Vejvalkova, Filip Fencl, et al.
European Journal of Pediatrics|September 25, 2012
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 geneFilip Fencl, Květa Bláhová, Karl Peter Schlingmann, et al.
Frontiers in Pediatrics|June 23, 2023
Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature reviewJakub Zieg, Terezia Tavačová, Miroslava Balaščáková, et al.
European Journal of Pediatrics|May 27, 2011
Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndromeFilip Fencl, Michal Malina, Veronika Stará, et al.
Casopis Lekaru Ceskych|October 11, 2017
[Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes]Jan Lebl, Lukáš Plachý, Květa Bláhová, et al.
Pediatric Nephrology (Berlin, Germany)|February 6, 2009
Genotype-phenotype correlation in children with autosomal dominant polycystic kidney diseaseFilip Fencl, Jan Janda, Kveta Bláhová, et al.
European Journal of Pediatrics|September 26, 2018
Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary studyLucia Karnisova, Ondrej Hradsky, Kveta Blahova, et al.
Klinische Padiatrie|July 31, 2025
Reduction of Parenteral Nutrition in Children with Short Bowel Syndrome Treated with Teduglutide: Experience from the Czech RepublicSarka Peskova, Astrida Sulakova, Katerina Bajerova, et al.
Pediatric Nephrology (Berlin, Germany)|December 20, 2022
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertensionTomáš Seeman, Kveta Bláhová, Filip Fencl, et al.
Plos One|June 24, 2020
Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosisLena Obeidova, Tomas Seeman, Filip Fencl, et al.
Pageof 3