List of works by Katarzyna Niepokój

Analysis of causes and treatment of hearing loss in children from Department of Infant Diseases the Children's Memorial Health Institute, Warsaw

scientific article published in January 2011

CHRONIC PANCREATITIS IN A PATIENT WITH THE p.Asn34Ser HOMOZYGOUS SPINK1 MUTATION--OWN EXPERIENCE.

scientific article published in July 2015

Gene conversion between cationic trypsinogen (PRSS1) and the pseudogene trypsinogen 6 (PRSS3P2) in patients with chronic pancreatitis

scientific article

Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.

scientific article published on 18 November 2017

Novel and recurrent COL7A1 mutation in a Polish population

scientific article published on 01 January 2012

Novel and recurrent variants of ATP2C1 identified in patients with Hailey-Hailey disease

scientific article published on 25 January 2020

Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation

scientific article published on 2 October 2015

Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics

scientific article

[Inherited skin diseases - a review of selected genodermatoses]

scientific article published on 01 July 2012

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