Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Cohort-based association study of germline genetic variants with acute and chronic health complications of childhood cancer and its treatment: Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study protocol

Autor: Nicolas Waespe, Sven Strebel, Tiago Nava, Chakradhara Rao S Uppugunduri, Denis Marino, Veneranda Mattiello, Maria Otth, Fabienne Gumy-Pause, André O Von Bueren, Frederic Baleydier, Luzius Mader, Adrian Spoerri, Claudia E Kuehni, Marc Ansari

Publikováno v: BMJ Open, Vol 12, Iss 1 (2022)
BMJ Open
Waespe, Nicolas; Strebel, Sven; Nava, Tiago; Uppugunduri, Chakradhara Rao S; Marino, Denis; Mattiello, Veneranda; Otth, Maria; Gumy-Pause, Fabienne; Von Bueren, André O; Baleydier, Frederic; Mader, Luzius; Spoerri, Adrian; Kuehni, Claudia E; Ansari, Marc (2022). Cohort-based association study of germline genetic variants with acute and chronic health complications of childhood cancer and its treatment: Genetic Risks for Childhood Cancer Complications Switzerland (GECCOS) study protocol. BMJ open, 12(1), e052131. BMJ Publishing Group 10.1136/bmjopen-2021-052131

IntroductionChildhood cancer and its treatment may lead to various health complications. Related impairment in quality of life, excess in deaths and accumulated healthcare costs are relevant. Genetic variations are suggested to contribute to the wide

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91a5b5a14aa0f272595215507427877
https://bmjopen.bmj.com/content/12/1/e052131.full

Epidemiology, aetiology, interventions and genomics in children with arthrogryposis multiplex congenita: protocol for a multisite registry

Autor: Noémi Dahan-Oliel, Harold van Bosse, Vasiliki Betty Darsaklis, Frank Rauch, Tanya Bedard, Ghalib Bardai, Michelle James, Ellen Raney, Krister Freese, Lauren Hyer, Haluk Altiok, Jonathan Pellett, Philip Giampietro, Judith Hall, Reggie Charles Hamdy

Publikováno v: BMJ open, vol 12, iss 10

IntroductionArthrogryposis multiplex congenita (AMC) is an umbrella term including hundreds of conditions with the common clinical manifestation of multiple congenital contractures. AMC affects 1 in 3000 live births and is caused by lack of movement

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a13e6bf0799fd75616fcce5612a7c043
https://doi.org/10.1136/bmjopen-2021-060591

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.