Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anna Szoszkiewicz"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-21 (2024)
Abstract Vertebral malformations (VMs) pose a significant global health problem, causing chronic pain and disability. Vertebral defects occur as isolated conditions or within the spectrum of various congenital disorders, such as Klippel–Feil syndro
Externí odkaz:
https://doaj.org/article/711aa8083926476e936d8852e29436fd
Autor:
Anna Sowińska-Seidler, Magdalena Socha, Anna Szoszkiewicz, Anna Materna-Kiryluk, Aleksander Jamsheer
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: Split-hand/foot malformation type 1 (SHFM1) refers to the group of rare congenital limb disorders defined by the absence or hypoplasia of the central rays of the autopods with or without accompanying anomalies, such as hearing loss, crani
Externí odkaz:
https://doaj.org/article/c356fd9be67a45c69532cb8d09bcf961
Autor:
Aleksandra Majchrzak-Celińska, Robert Kleszcz, Elżbieta Studzińska-Sroka, Agnieszka Łukaszyk, Anna Szoszkiewicz, Ewelina Stelcer, Karol Jopek, Marcin Rucinski, Judyta Cielecka-Piontek, Violetta Krajka-Kuźniak
Publikováno v:
Cells, Vol 11, Iss 7, p 1084 (2022)
Lichens are a source of secondary metabolites with significant pharmacological potential. Data regarding their possible application in glioblastoma (GBM) treatment are, however, scarce. The study aimed at analyzing the mechanism of action of six lich
Externí odkaz:
https://doaj.org/article/671d936ba46b436aa2b59f37cf135a9c
Publikováno v:
Journal of applied genetics.
Partial 16p trisomy syndrome is a rare disorder typically characterized by psychomotor retardation, prenatal and postnatal growth deficiency, cleft palate, and facial dysmorphism, with some patients also presenting with heart defects and urogenital a