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Author

Filip Fencl

Observed names: F Fencl, F. Fencl, Fencl Filip, Fencl, Filip
ORCID: 0000-0002-8106-1037
Observed ORCID: 0000-0002-8106-1037
OpenAlex ID: A5069764573
Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene
2012 · Filip Fencl, Květa Bláhová, et al. · European Journal of Pediatrics · 60
Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene
2008 · Barbora Obermannova, Karolina Banghova, et al. · European Journal of Pediatrics · 50
HomozygousEXOSC3Mutation c.92G→C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma
2013 · Jaroslava Schwabova, Dana Safka Brozkova, et al. · Journal of Neurogenetics · 44
Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease
2009 · Filip Fencl, Jan Janda, et al. · Pediatric Nephrology · 41
Recurrence of Nephrotic Proteinuria in Children With Focal Segmental Glomerulosclerosis After Renal Transplantation Treated With Plasmapheresis and Immunoadsorption: Case Reports
2007 · F. Fencl, E. S̆imková, et al. · Transplantation Proceedings · 26
Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis
2020 · Lena Obeidova, Tomas Seeman, et al. · PLoS ONE · 23
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Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement
2019 · Renata Formankova, Veronika Kanderova, et al. · Frontiers in Immunology · 19
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Complement activation is associated with more severe course of diarrhea-associated hemolytic uremic syndrome, a preliminary study
2018 · Lucia Karnisova, Ondrej Hradsky, et al. · European Journal of Pediatrics · 19
Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome
2011 · Filip Fencl, Michal Malina, et al. · European Journal of Pediatrics · 17
A novel heterozygous RIT1 mutation in a patient with Noonan syndrome, leukopenia, and transient myeloproliferation—a review of the literature
2015 · Michaela Nemcikova, Sarka Vejvalkova, et al. · European Journal of Pediatrics · 15
Recurrence of nephrotic proteinuria in children with focal segmental glomerulosclerosis: early treatment with plasmapheresis and immunoadsorption should be associated with better prognosis.
2016 · Filip Fencl, Karel Vondrák, et al. · PubMed · 13
McCune Albright syndrome and bilateral adrenal hyperplasia: the GNAS mutation may only be present in adrenal tissue
2015 · Anna Angelousi, Filip Fencl, et al. · HORMONES · 12
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B cell phenotype and serum levels of interferons, BAFF, and APRIL in multisystem inflammatory syndrome in children associated with COVID-19 (MIS-C)
2023 · Adam Klocperk, Marketa Bloomfield, et al. · Molecular and Cellular Pediatrics · 10
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Increasing prevalence of hypertension during long-term follow-up in children with autosomal dominant polycystic kidney disease
2021 · Tomáš Seeman, Petr Jansky, et al. · Pediatric Nephrology · 8
Kidney concentrating capacity in children with autosomal recessive polycystic kidney disease is linked to glomerular filtration and hypertension
2022 · Tomáš Seeman, Kveta Bláhová, et al. · Pediatric Nephrology · 6
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Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion
2024 · Marketa Rackova, Rafael Mattera, et al. · Journal of Molecular Medicine · 5
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Sudden cardiac arrest in a child with Gitelman syndrome: a case report and literature review
2023 · Jakub Zieg, Terezia Tavačová, et al. · Frontiers in Pediatrics · 5
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Alteration in DNA-binding affinity of Wilms tumor 1 protein due to WT1 genetic variants associated with steroid - resistant nephrotic syndrome in children
2022 · Martin Bezdicka, Filip Kaufman, et al. · Scientific Reports · 5
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Blood pressure in children with renal cysts and diabetes syndrome
2021 · Tomáš Seeman, Friederike Weigel, et al. · European Journal of Pediatrics · 4
Posterior Reversible Encephalopathy Syndrome – A Rare Complication of COVID-19 MIS-C
2022 · Jan David, Ledjona Toni, et al. · Klinische Pädiatrie · 3
Life-threatening Manifestations of Vitamin B12 Deficiency in Infants on a Vegan Diet
2021 · Jan David, Filip Fencl · Klinische Pädiatrie · 3
Correlation between knee roentgenogram changes and clinical symptoms in osteoarthritis.
1992 · K Pavelka, J Gatterová, et al. · PubMed · 2
Rhabdomyolysis in children
2020 · Jan David, Michaela Šibíková, et al. · Pediatrie pro praxi · 1
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Inferior Vena Cava Filters in Adolescents with Thromboembolic Disease: Technical Outcomes, Retrieval, and the Role of Skeletal Maturity
2026 · Tomas Melis, Radek Padr, et al. · Journal of Vascular and Interventional Radiology
Serum and urinary D-lactate in pediatric intestinal failure: clinical associations and reference values
2026 · Rita Halašová, Rana Ibrahim, et al. · Pediatric Research
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Works count: 31
Citation count: 391
H-index: 12
I10-index: 13
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