Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Łukasz, Kępczyński"'
Autor:
Daria Gierach, Łukasz Kępczyński
Publikováno v:
Przegląd Dermatologiczny, Vol 110, Iss 4, Pp 567-573 (2023)
Externí odkaz:
https://doaj.org/article/22805b47b37f4a82a5e5716c0622d25f
Autor:
Agata Kucińska, Wanda Hawuła, Lena Rutkowska, Urszula Wysocka, Łukasz Kępczyński, Małgorzata Piotrowicz, Tatiana Chilarska, Nina Wieczorek-Cichecka, Katarzyna Połatyńska, Łukasz Przysło, Agnieszka Gach
Publikováno v:
Brain Sciences, Vol 14, Iss 6, p 529 (2024)
In the original publication [...]
Externí odkaz:
https://doaj.org/article/7c4b047a288746fb81c6ec2e98d34646
Autor:
Kinga Sałacińska, Iwona Pinkier, Lena Rutkowska, Danuta Chlebna-Sokół, Elżbieta Jakubowska-Pietkiewicz, Izabela Michałus, Łukasz Kępczyński, Dominik Salachna, Nina Wieczorek-Cichecka, Małgorzata Piotrowicz, Tatiana Chilarska, Aleksander Jamsheer, Paweł Matusik, Małgorzata Wilk, Elżbieta Petriczko, Maria Giżewska, Iwona Stecewicz, Mieczysław Walczak, Magda Rybak-Krzyszkowska, Andrzej Lewiński, Agnieszka Gach
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Osteogenesis imperfecta (OI) is a rare genetic disorder of the connective tissue. It presents with a wide spectrum of skeletal and extraskeletal features, and ranges in severity from mild to perinatal lethal. The disease is characterized by a heterog
Externí odkaz:
https://doaj.org/article/f46f73cf625d46ddb2885a7702d86c5c
Autor:
Agata Kucińska, Wanda Hawuła, Lena Rutkowska, Urszula Wysocka, Łukasz Kępczyński, Małgorzata Piotrowicz, Tatiana Chilarska, Nina Wieczorek-Cichecka, Katarzyna Połatyńska, Łukasz Przysło, Agnieszka Gach
Publikováno v:
Brain Sciences, Vol 14, Iss 3, p 273 (2024)
Autism spectrum disorders (ASDs) encompass a broad group of neurodevelopmental disorders with varied clinical symptoms, all being characterized by deficits in social communication and repetitive behavior. Although the etiology of ASD is heterogeneous
Externí odkaz:
https://doaj.org/article/0ebf1a4289cd4ffb8a9329a9e541b01c
Autor:
Kinga Sałacińska, Izabela Michałus, Iwona Pinkier, Lena Rutkowska, Danuta Chlebna‐Sokół, Elżbieta Jakubowska‐Pietkiewicz, Łukasz Kępczyński, Dominik Salachna, Agnieszka Gach
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Background Osteogenesis imperfecta (OI) is a genetic disorder of connective tissue with variable phenotype and heterogeneous genetic background. Majority of reported mutations are glycine substitutions, whose clinical outcome ranges from mil
Externí odkaz:
https://doaj.org/article/d6f1f8f7e9954f2a972ca884ec1ee2d5
Autor:
Łukasz Kępczyński, Szymon Wcisło, Irmina Korzeniewska-Dyl, Katarzyna Połatyńska, Agnieszka Gach, Dariusz Moczulski
Publikováno v:
Adipocyte, Vol 10, Iss 1, Pp 153-159 (2021)
TBC1D1 and TBC1D4 proteins play analogous, but not identical role in governing insulin-signalling pathway. Little is known about changes in expression levels of TBC1D1 and TBC1D4 genes in mammals, including humans. Number of factors were studied, but
Externí odkaz:
https://doaj.org/article/a1c5a3b24d2942b3bdeb251b5d099437
Autor:
Katarzyna Połatyńska, Łukasz Kępczyński, Marta Jankowska, Magdalena Pokorska, Piotr Grzelak, Łukasz Przysło
Publikováno v:
Pediatric Anesthesia and Critical Care Journal (PACCJ), Vol 8, Iss 2, Pp 129-132 (2020)
This report presents first case of severe multi-organ trauma, complicated with SARS-CoV-2 infection. The child suffered from trauma resulting from falling out of the window. Imaging revealed head trauma, areas of lung contusion and abdominal organ tr
Externí odkaz:
https://doaj.org/article/726f77caa7094b6185d8a99d05e49421
Autor:
Łukasz Kępczyński, Katarzyna Połatyńska, Anna Nykel, Jordan Sałamunia, Tadeusz Kałużewski, Andrzej Kużawczyk, Agnieszka Gach
Publikováno v:
Menopause Review, Vol 19, Iss 4, Pp 171-173 (2021)
Externí odkaz:
https://doaj.org/article/c80f8ccf58c5486896125aae80c2a4cf
Autor:
Kinga Sałacińska, Iwona Pinkier, Lena Rutkowska, Danuta Chlebna-Sokół, Elżbieta Jakubowska-Pietkiewicz, Izabela Michałus, Łukasz Kępczyński, Dominik Salachna, Aleksander Jamsheer, Ewelina Bukowska-Olech, Ilona Jaszczuk, Lucjusz Jakubowski, Agnieszka Gach
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
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 is recogniz
Externí odkaz:
https://doaj.org/article/6b234bb895cc4552bbacaa244b5a5826
Publikováno v:
Studia Medyczne, Vol 35, Iss 4, Pp 312-318 (2019)
The symmetry of a newborn baby’s head and face, including the symmetry of a palpebral fissure, auricles, nose, and the movement of eyelids and mouth, is evaluated during a newborn baby’s overall examination. Asymmetric crying facies (ACF) is a co
Externí odkaz:
https://doaj.org/article/5a08dfe31b954a7b8231ccf04ea07ff2