Denisa Ilencikova
Bratislava, BL, Slovakia
Last Updated: 09/26/2026
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Found 27 publications
Myhre Syndrome Associated With Dunbar Syndrome and Urinary Tract Abnormalities: A Case Report.
Journal: Frontiers in pediatrics
Published: September 10, 2019
Chronic pancreatitis with polycystic kidney disease: A rare coincidence?
Journal: Nefrologia
Published: April 10, 2019
TRIM28 haploinsufficiency predisposes to Wilms tumor.
Journal: International journal of cancer
Published: October 08, 2018
Somatic mosaic monosomy 7 and UPD7q in a child with MIRAGE syndrome caused by a novel SAMD9 mutation.
Journal: Pediatric blood & cancer
Published: July 25, 2018
No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.
Journal: Frontiers in immunology
Published: March 23, 2018
Terminal 14q32.33 deletion as a novel cause of agammaglobulinemia.
Journal: Clinical immunology (Orlando, Fla.)
Published: July 02, 2017
High Yield of Pathogenic Germline Mutations Causative or Likely Causative of the Cancer Phenotype in Selected Children with Cancer.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: June 16, 2017
The first Slovak Legius syndrome patient carrying the SPRED1 gene mutation.
Journal: General physiology and biophysics
Published: May 02, 2016
Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection.
Journal: General physiology and biophysics
Published: October 13, 2015
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations.
Journal: Annals of human genetics
Published: April 19, 2015
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Journal: Gastroenterology
Published: February 19, 2015
Last Updated: 09/26/2026