Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Veneranda Mattiello"'
Autor:
Nicolas Waespe, Sven Strebel, Denis Marino, Veneranda Mattiello, Fanny Muet, Tiago Nava, Christina Schindera, Fabien N. Belle, Luzius Mader, Adrian Spoerri, Claudia E. Kuehni, Marc Ansari
Publikováno v:
BMC Medical Research Methodology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Research on germline genetic variants relies on enough eligible participants which is difficult to achieve for rare diseases such as childhood cancer. With self-collection kits, participants can contribute genetic samples convenie
Externí odkaz:
https://doaj.org/article/e689c70912504f71b6d0877e5485ef61
Autor:
Claudia E Kuehni, André O von Bueren, Adrian Spoerri, Maria Otth, Nicolas Waespe, Sven Strebel, Tiago Nava, Chakradhara Rao S Uppugunduri, Denis Marino, Veneranda Mattiello, Fabienne Gumy-Pause, Frederic Baleydier, Luzius Mader, Marc Ansari
Publikováno v:
BMJ Open, Vol 12, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/1625ca1818dc40fcb7c8f626c2573d10
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
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
Autor:
Veneranda Mattiello, Stéphane Sizonenko, Fréderic Baleydier, Fanette Bernard, Manuel Diezi, Raffaele Renella
Publikováno v:
Revue Médicale Suisse. 15:376-381
Autor:
Denis Marino, Tiago Nava, Claudia E. Kuehni, Marc Ansari, Adrian Spoerri, Christina Schindera, Veneranda Mattiello, Nicolas Waespe, Luzius Mader, Fabiën N. Belle, Sven Strebel, Fanny Muet
Publikováno v:
BMC Medical research methodology, Vol. 21, No 1 (2021) P. 236
BMC Medical Research Methodology, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Medical Research Methodology
Waespe, Nicolas; Strebel, Sven; Marino, Denis; Mattiello, Veneranda; Muet, Fanny; Nava, Tiago; Schindera, Christina; Belle, Fabien N.; Mader, Luzius; Spoerri, Adrian; Kuehni, Claudia E.; Ansari, Marc (2021). Predictors for participation in DNA self-sampling of childhood cancer survivors in Switzerland. BMC Medical research methodology, 21(1), p. 236. BioMed Central 10.1186/s12874-021-01428-1
BMC Medical Research Methodology, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Medical Research Methodology
Waespe, Nicolas; Strebel, Sven; Marino, Denis; Mattiello, Veneranda; Muet, Fanny; Nava, Tiago; Schindera, Christina; Belle, Fabien N.; Mader, Luzius; Spoerri, Adrian; Kuehni, Claudia E.; Ansari, Marc (2021). Predictors for participation in DNA self-sampling of childhood cancer survivors in Switzerland. BMC Medical research methodology, 21(1), p. 236. BioMed Central 10.1186/s12874-021-01428-1
Background Research on germline genetic variants relies on enough eligible participants which is difficult to achieve for rare diseases such as childhood cancer. With self-collection kits, participants can contribute genetic samples conveniently from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcdef057a71866b85dcacb8a1af2cb51
https://archive-ouverte.unige.ch/unige:157186
https://archive-ouverte.unige.ch/unige:157186
Autor:
Markus Schmugge, Nicolas von der Weid, Veneranda Mattiello, Heinz Hengartner, Raffaele Renella
Publikováno v:
Pediatric bloodcancerREFERENCES. 68(3)
Autor:
Nicolas von der Weid, Markus Schmugge, Raffaele Renella, Heinz Hengartner, Veneranda Mattiello
Iron deficiency is the most prevalent nutritional deficiency affecting children and adolescents worldwide. A consistent body of epidemiological data demonstrates an increased incidence of iron deficiency at three timepoints: in the neonatal period, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66e0ddfaf750a4ce3897a9fcb9f66624
https://www.zora.uzh.ch/id/eprint/199946/
https://www.zora.uzh.ch/id/eprint/199946/
Autor:
Veneranda, Mattiello, Stéphane, Sizonenko, Fréderic, Baleydier, Fanette, Bernard, Manuel, Diezi, Raffaele, Renella
Publikováno v:
Revue medicale suisse. 15(638)
Non anemic iron deficiency (NAID) is the most common nutritional deficiency. Symptoms more frequently observed in children and adolescents include fatigue, delayed psychomotor development as well as decreased school and athletic performances. Iron tr
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