Ilona Jaszczuk
Overview
Explore the profile of Ilona Jaszczuk including associated specialties, affiliations and a list of published articles.
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13
Citations
59
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Recent Articles
1.
Wertheim-Tysarowska K, Osipowicz K, Wozniak K, Sawicka J, Mika A, Kutkowska-Kazmierczak A, et al.
Orphanet J Rare Dis
. 2024 Nov;
19(1):413.
PMID: 39501396
Background: The Mendelian Disorders of Cornification (MeDOC) comprise a large number of disorders that present with either localised (palmoplantar keratoderma, PPK) or generalised (ichthyoses) signs. The MeDOC are highly heterogenic...
2.
Kondracka A, Kondracki B, Jaszczuk I, Staniczek J, Kwasniewski W, Filip A, et al.
Ginekol Pol
. 2023 Apr;
95(12):952-958.
PMID: 37042323
Objectives: MicroRNAs have been observed to play a major role in various physiological processes, for instance, programmed cell death, cell division, pregnancy development, and proliferation. With the help of profiling...
3.
Kondracka A, Jaszczuk I, Koczkodaj D, Kondracki B, Fraszczak K, Oniszczuk A, et al.
J Clin Med
. 2022 Dec;
11(23).
PMID: 36498625
Preeclampsia and hypertension complicate several pregnancies. Identifying women at risk of developing these conditions is essential to establish potential treatment modalities. Biomarkers such as C19MC microRNA in pregnant patients wopuld...
4.
Jaszczuk I, Winkler I, Koczkodaj D, Skrzypczak M, Filip A
Int J Mol Sci
. 2022 Nov;
23(22).
PMID: 36430313
Pre-eclampsia is a placenta-related complication occurring in 2-10% of all pregnancies. miRNAs are a group of non-coding RNAs regulating gene expression. There is evidence that C19MC miRNAs are involved in...
5.
Winkler I, Jaszczuk I, Gogacz M, Szkodziak P, Paszkowski T, Skorupska K, et al.
Int J Environ Res Public Health
. 2022 May;
19(9).
PMID: 35564421
Background: The aim of the present study is to report a rare occurrence of a successful twin pregnancy in a woman with pure 46,XY gonadal dysgenesis. Result(s): A patient with...
6.
Jaszczuk I, Koczkodaj D, Kondracka A, Kwasniewska A, Winkler I, Filip A
Ann Med
. 2022 May;
54(1):1350-1356.
PMID: 35543206
MicroRNAs (miRNAs) are a class of small non-coding, single-stranded RNAs (ribonucleic acids) that play important roles in many vital processes through their impact on gene expression. One such miRNA, miR210,...
7.
Salacinska K, Pinkier I, Rutkowska L, Chlebna-Sokol D, Jakubowska-Pietkiewicz E, Michalus I, et al.
Front Genet
. 2021 Jul;
12:692978.
PMID: 34306033
Osteogenesis imperfecta (OI) is a rare genetic disorder demonstrating considerable phenotypic and genetic heterogeneity. The extensively studied genotype-phenotype correlation is a crucial issue for a reliable counseling, as the disease...
8.
Winkler I, Miotla P, Lejman M, Pietrzyk A, Kacprzak M, Kubiak M, et al.
BMC Med Genomics
. 2021 May;
14(1):131.
PMID: 34006278
Background: Autosomal recessive mutations in the AP-4 (adaptor protein complex 4) complex subunit ϵ - 1 (AP-4E1) gene on chromosome 15q21.2 are known to cause spastic paraplegia 51 (SPG51). The...
9.
Szelest M, Stefaniak M, Reka G, Jaszczuk I, Lejman M
BMC Med Genomics
. 2021 Mar;
14(1):76.
PMID: 33691695
Background: 16p11.2 microdeletion is a known chromosomal anomaly associated mainly with neurocognitive developmental delay, predisposition to obesity, and variable dysmorphism. Although this deletion is relatively rare among the general population,...
10.
Poluha A, Bernaciak J, Jaszczuk I, Kedzior M, Nowakowska B
Mol Cytogenet
. 2017 Sep;
10:34.
PMID: 28912834
Background: Three distinct contiguous gene deletion syndromes are located at 10p chromosomal region. The deletion, involving 10p15.3 region, has been characterized by (DeScipio et al., Am J Med Genet A...