Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tomáš Sláma"'
Autor:
Eva-Maria Hau, Tomáš Sláma, Stefan Essig, Gisela Michel, Laura Wengenroth, Eva Bergstraesser, Nicolas X. von der Weid, Christina Schindera, Claudia E. Kuehni
Publikováno v:
BMC Primary Care, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Epidemiological studies often rely on self-reported health problems and validation greatly improves study quality. In a study of late effects after childhood cancer, we validated self-reported cardiovascular problems by contacting
Externí odkaz:
https://doaj.org/article/25acb7907f6f4ef7aa6c946161204cb2
Autor:
Sven Strebel, Luzius Mader, Tomáš Sláma, Nicolas Waespe, Annette Weiss, Ross Parfitt, Antoinette am Zehnhoff‐Dinnesen, Martin Kompis, Nicolas X. von der Weid, Marc Ansari, Claudia E. Kuehni
Publikováno v:
Strebel, Sven; Mader, Luzius; Sláma, Tomáš; Waespe, Nicolas; Weiss, Annette; Parfitt, Ross; Am Zehnhoff-Dinnesen, Antoinette; Kompis, Martin; von der Weid, Nicolas X; Ansari, Marc; Kuehni, Claudia E (2022). Severity of hearing loss after platinum chemotherapy in childhood cancer survivors. Pediatric blood & cancer, 69(9), e29755. Wiley-Liss 10.1002/pbc.29755
BACKGROUND Hearing loss is a potential side effect from childhood cancer treatment. We described the severity of hearing loss assessed by audiometry in a representative national cohort of childhood cancer survivors (CCS) and identified clinical risk
Autor:
Luzius Mader, Tomáš Sláma, Christina Schindera, Jochen Rössler, Nicolas X von der Weid, Fabiën N Belle, Claudia E Kuehni
Publikováno v:
Mader, Luzius; Sláma, Tomáš; Schindera, Christina; Rössler, Jochen; von der Weid, Nicolas X; Belle, Fabiën N; Kuehni, Claudia E (2022). Social, emotional, and behavioral functioning in young childhood cancer survivors with chronic health conditions. Pediatric blood & cancer, 69(9), e29756. Wiley-Liss 10.1002/pbc.29756
BACKGROUND The cancer diagnosis and its intensive treatment may affect the long-term psycho-social adjustment of childhood cancer survivors. We aimed to describe social, emotional, and behavioral functioning and their determinants in young childhood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4d020150386de23085c09f48891add6
Publikováno v:
Journal of Inherited Metabolic Disease. 42:295-302
Galactosialidosis (GS; OMIM #256540) is a rare multisystemic inborn glycoprotein storage disease caused by biallelic mutations in the cathepsin A gene resulting in combined deficiency of the lysosomal enzymes β-galactosidase and α-neuraminidase. Th
Autor:
Katrin Hinderhofer, Stefan Kölker, Georg F. Hoffmann, Konstantin Mechler, Markus Ries, William K Mountford, Shoko Komatsuzaki, Sven F. Garbade, Matthias Zielonka, Tomáš Sláma, Eugen Mengel
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 44(1)
The natural history of most rare diseases is incompletely understood and usually relies on studies with low level of evidence. Consistent with the goals for future research of rare disease research set by the International Rare Diseases Research Cons
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