Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Teresa Schätzl"'
Autor:
Teresa Schätzl, Vanessa Todorow, Lars Kaiser, Helga Weinschrott, Benedikt Schoser, Hans-Peter Deigner, Peter Meinke, Matthias Kohl
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-14 (2024)
Abstract Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common autosomal dominant muscle disorders, yet no cure or amelioration exists. The clinical presentation is diverse, making it difficult to identify the actual driving pathome
Externí odkaz:
https://doaj.org/article/37e93bddba1946c9ac887873619d2419
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 17, p 9344 (2024)
Atopic dermatitis (AD) is a common inflammatory skin disease, in particular among infants, and is characterized, among other things, by a modification in fatty acid and ceramide composition of the skin’s stratum corneum. Palmitic acid and stearic a
Externí odkaz:
https://doaj.org/article/43be2a06536a4ddda7c81da615183311
Autor:
Teresa Gerhalter, Christina Müller, Elke Maron, Markus Thielen, Teresa Schätzl, Anja Mähler, Till Schütte, Michael Boschmann, René Herzer, Simone Spuler, Elisabetta Gazzerro
Publikováno v:
Frontiers in Physiology, Vol 14 (2023)
Objective: In the field of non-treatable muscular dystrophies, promising new gene and cell therapies are being developed and are entering clinical trials. Objective assessment of therapeutic effects on motor function is mandatory for economical and e
Externí odkaz:
https://doaj.org/article/52da30c9c13740d991f389719653d0cb
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-26 (2021)
Abstract Whilst a disease-modifying treatment for Facioscapulohumeral muscular dystrophy (FSHD) does not exist currently, recent advances in complex molecular pathophysiology studies of FSHD have led to possible therapeutic approaches for its targete
Externí odkaz:
https://doaj.org/article/6962fa1e9abd4ab3a1e09d7a1e621d29