Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Łukasz Kuszel"'
Autor:
Joanna Walczak-Sztulpa, Anna Wawrocka, Łukasz Kuszel, Paulina Pietras, Marta Leśniczak-Staszak, Mirosław Andrusiewicz, Maciej R. Krawczyński, Anna Latos-Bieleńska, Marta Pawlak, Ryszard Grenda, Anna Materna-Kiryluk, Machteld M. Oud, Witold Szaflarski
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: 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 insufficien
Externí odkaz:
https://doaj.org/article/0e0d5cf622d04179ab39c703254bd1dc
Publikováno v:
Vaccines, Vol 11, Iss 1, p 118 (2023)
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 pathogens in the respiratory tract. Therefor
Externí odkaz:
https://doaj.org/article/9b3244c3b9da49f1bf3e40c4d33cdace
Autor:
Szymon P. Nowak, Paweł Zmora, Łukasz Pielok, Łukasz Kuszel, Ryszard Kierzek, Jerzy Stefaniak, Małgorzata Paul
Publikováno v:
Emerging Infectious Diseases, Vol 25, Iss 9, Pp 1772-1773 (2019)
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 of the parasite in Giemsa-stained microscopic smea
Externí odkaz:
https://doaj.org/article/0690ac81a31b42039787d76576471ec8
Publikováno v:
Journal of Applied Genetics.
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 of the disease in its advanced stage. Despite innovative diagnostic methods a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2480a90f4fee7e0320cd9df9b457ff03
https://doi.org/10.1007/s13353-023-00750-2
https://doi.org/10.1007/s13353-023-00750-2
Autor:
Magdalena Badura-Stronka, Łukasz Kuszel, Agnieszka Wencel-Warot, Kamila Cudnoch, Katarzyna Wołyńska, Karolina Rutkowska, Barbara Steinborn, Rafał Płoski
Publikováno v:
Epilepsy Research. 190:107101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59a5d53f97b743e4c61b569315d829e0
https://doi.org/10.1016/j.eplepsyres.2023.107101
https://doi.org/10.1016/j.eplepsyres.2023.107101
Autor:
Joanna Walczak-Sztulpa, Aleksander Jamsheer, Maciej R Krawczyński, Łukasz Kuszel, Magdalena Socha, Anna Skorczyk-Werner, Anna Wawrocka
Publikováno v:
Klinika Oczna. 2018:189-194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddc523b69b460c983552ad250ad1fcbb
https://doi.org/10.5114/ko.2018.82893
https://doi.org/10.5114/ko.2018.82893
Autor:
Magdalena Badura-Stronka, Anna Winczewska-Wiktor, Sarah I. Garry, Samuel F. Berkovic, Barbara Steinborn, Monika Starczewska, Jozef Gecz, Sunita Koirala, Alison Gardner, Marie Shaw, Łukasz Kuszel, Piotr Kowal, Ingrid E. Scheffer
Publikováno v:
European Journal of Medical Genetics. 63:103799
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 also been described as a poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39a1d8fc7f0dda32f00c97fa70f0258
https://doi.org/10.1016/j.ejmg.2019.103799
https://doi.org/10.1016/j.ejmg.2019.103799
Autor:
Paweł Zmora, Szymon Nowak, Ryszard Kierzek, Łukasz Pielok, Małgorzata Paul, Łukasz Kuszel, Jerzy Stefaniak
Publikováno v:
Emerging Infectious Diseases
Emerging Infectious Diseases, Vol 25, Iss 9, Pp 1772-1773 (2019)
Emerging Infectious Diseases, Vol 25, Iss 9, Pp 1772-1773 (2019)
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 of the parasite in Giemsa-stained microscopic smea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3da5dc6142c499216de6efda645ae64e
http://europepmc.org/articles/PMC6711224
http://europepmc.org/articles/PMC6711224
Autor:
Anna Wawrocka, Joanna Walczak-Sztulpa, Lukasz Kuszel, Zuzanna Niedziela-Schwartz, Anna Skorczyk-Werner, Jadwiga Bernardczyk-Meller, Maciej R. Krawczynski
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 5759 (2024)
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 as nonsyndromic or syndromic with complex
Externí odkaz:
https://doaj.org/article/a5abbf4d9d5947d68d3b4161e94a8bca
Autor:
Dagny Lorent, Rafal Nowak, Carolina Roxo, Elzbieta Lenartowicz, Aleksandra Makarewicz, Bartosz Zaremba, Szymon Nowak, Lukasz Kuszel, Jerzy Stefaniak, Ryszard Kierzek, Pawel Zmora
Publikováno v:
Vaccines, Vol 9, Iss 6, p 541 (2021)
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 (SARS-CoV-2) infections. To estimate the scale
Externí odkaz:
https://doaj.org/article/83b267b0e71a48f9bef8bd8b54a22037