Lukasz Kuszel
Overview
Explore the profile of Lukasz Kuszel including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
17
Citations
86
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Wawrocka A, Walczak-Sztulpa J, Kuszel L, Niedziela-Schwartz Z, Skorczyk-Werner A, Bernardczyk-Meller J, et al.
Int J Mol Sci
. 2024 Jun;
25(11).
PMID: 38891946
Retinitis pigmentosa (RP) is an inherited retinal dystrophy caused by the loss of photoreceptors and retinal pigment epithelial atrophy, leading to severe visual impairment or blindness. RP can be classified...
2.
Kuszel L, Trzeciak T, Begier-Krasinska B, Richter M, Li J, Czarny-Ratajczak M
J Cell Mol Med
. 2024 Jan;
28(3):e18107.
PMID: 38235989
Accelerated telomere shortening is associated with age-related diseases, including osteoarthritis (OA). We aimed to determine the relative telomere length (TL) in leukocytes and cartilage of patients with primary knee OA...
3.
Walczak-Sztulpa J, Wawrocka A, Kuszel L, Pietras P, Lesniczak-Staszak M, Andrusiewicz M, et al.
Front Mol Biosci
. 2024 Jan;
10:1285790.
PMID: 38161384
Cranioectodermal dysplasia (CED) is a skeletal autosomal recessive ciliopathy. The characteristic clinical features of CED are facial dysmorphisms, short limbs, narrow thorax, brachydactyly, ectodermal abnormalities, and renal insufficiency. Thus far,...
4.
Frydrychowicz M, Kuszel L, Dworacki G, Budna-Tukan J
J Appl Genet
. 2023 Feb;
64(3):459-477.
PMID: 36821071
Lung cancer is the most common cause of cancer-related deaths in the world. One of the reasons of poor prognosis and high mortality of lung cancer patients is the diagnosis...
5.
Badura-Stronka M, Kuszel L, Wencel-Warot A, Cudnoch K, Wolynska K, Rutkowska K, et al.
Epilepsy Res
. 2023 Feb;
190:107101.
PMID: 36758444
Missense variants in the synaptic vesicle glycoprotein SV2A gene have been previously found in a few individuals with epilepsy. Adverse reaction to levetiracetam in individuals with various variants of this...
6.
Lorent D, Nowak R, Jankowska M, Kuszel L, Zmora P
Vaccines (Basel)
. 2023 Jan;
11(1).
PMID: 36679962
Children are among the best vectors to spread respiratory viruses, including emerging variants of SARS-CoV-2 due to the asymptomatic or relatively mild course of infection and simultaneously high titres of...
7.
Wawrocka A, Walczak-Sztulpa J, Socha M, Kuszel L, Sowinska-Seidler A, Budny B, et al.
Am J Med Genet A
. 2021 Nov;
188(2):642-647.
PMID: 34773354
Aniridia is usually an autosomal dominant, rare disorder characterized by a variable degree of hypoplasia or the absence of iris tissue, with additional ocular abnormalities. Pathogenic variants in the PAX6...
8.
Lorent D, Nowak R, Roxo C, Lenartowicz E, Makarewicz A, Zaremba B, et al.
Vaccines (Basel)
. 2021 Jun;
9(6).
PMID: 34064028
In comparison to other European countries, during the first months of the COVID-19 pandemic, Poland reported a relatively low number of confirmed cases of severe acute respiratory syndrome coronavirus 2...
9.
Shaw M, Winczewska-Wiktor A, Badura-Stronka M, Koirala S, Gardner A, Kuszel L, et al.
Eur J Med Genet
. 2019 Oct;
63(4):103799.
PMID: 31655144
Mutations in ATP6V1B2, which encodes the B2 subunit of the vacuolar H + ATPase have previously been associated with Zimmermann-Laband syndrome 2 (ZLS2) and deafness-onychodystrophy (DDOD) syndrome. Recently epilepsy has...
10.
Nowak S, Zmora P, Pielok L, Kuszel L, Kierzek R, Stefaniak J, et al.
Emerg Infect Dis
. 2019 Aug;
25(9):1772-1773.
PMID: 31441757
We report a case of Plasmodium knowlesi malaria imported to central Europe from Southeast Asia. Laboratory suspicion of P. knowlesi infection was based on the presence of atypical developmental forms...