Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Heinz, Hengartner"'
Autor:
Milenko Rakic, Heinz Hengartner, Sonja Lüer, Katrin Scheinemann, Bernice S. Elger, Michael Rost
Publikováno v:
Swiss Medical Weekly, Vol 152, Iss 3738 (2022)
BACKGROUND AND PURPOSE: Culturally diverse countries such as Switzerland face the challenge of providing cross-cultural competent care. Cross-cultural competent care needs an understanding of a patient's cultural context in order to provide safe and
Externí odkaz:
https://doaj.org/article/582bdf1de8824985ac8350a8ba6ef605
Autor:
Christian Kreis, Harris Héritier, Katrin Scheinemann, Heinz Hengartner, Kees de Hoogh, Martin Röösli, Ben D. Spycher
Publikováno v:
Environment International, Vol 166, Iss , Pp 107380- (2022)
Motor vehicle exhaust is a major contributor to air pollution, and exposure to benzene or other carcinogenic components may increase cancer risks. We aimed to investigate the association between traffic-related air pollution and risk of childhood can
Externí odkaz:
https://doaj.org/article/609669e63adf41b7a02e6d908b6b35e8
Publikováno v:
European journal of cancer care. 31(6)
In face of disparities in access to cancer care, it has been proposed to measure accessibility and to explore policy strategies for mitigating inequality of access. We aimed to determine the accessibility of Swiss paediatric oncology centres.We emplo
Autor:
Carlo R. Largiadèr, Thomas R. Braschler, Stefan Farese, Behrouz Mansouri Taleghani, Pierre-Yves Lovey, Heinz Hengartner, Johanna A. Kremer Hovinga, Florian Buchkremer, Erika Tarasco
Publikováno v:
Hämostaseologie. 40:S5-S14
The Hereditary TTP Registry is an international cohort study for patients with a confirmed or suspected diagnosis of hereditary thrombotic thrombocytopenic purpura (hTTP) and their family members. Hereditary TTP is an ultra-rare blood disorder (preva
Diamond-Blackfan anemia (DBA) is caused mainly by genetic mutations in large (RPL) or small ribosomal subunit genes (RPS) and presents with macrocytic anemia and congenital malformations. Clinical differences between genotypes are insufficiently unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4c2dda368e542d0bf4a5891e0823382
Autor:
Johanna A, Kremer Hovinga, Thomas R, Braschler, Florian, Buchkremer, Stefan, Farese, Heinz, Hengartner, Pierre-Yves, Lovey, Carlo R, Largiadèr, Behrouz, Mansouri Taleghani, Erika, Tarasco
Publikováno v:
Hamostaseologie. 40(S 01)
The
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:
Niklas Stabell, Michael A. Grotzer, Karolina Nemes, Stefan Rutkowski, Uwe Kordes, Veronica Biassoni, Maria Joao Gil-da-Costa, Paul-Gerhardt Schlegel, Pablo Hernáiz-Driever, Mona Steinbügl, Michael C. Frühwald, Harald Reinhard, Marianne D. van de Wetering, Beate Timmermann, Joachim Boos, Joachim Gerss, Monika Warmuth-Metz, Martin Hasselblatt, Rhoikos Furtwängler, Nicolas U. Gerber, Martha Perek-Polnik, Peter Hauser, Reinhard Schneppenheim, Jane Pears, Werner Paulus, Eduardo Quiroga, Reiner Siebert, Stefan Tippelt, Heinz Hengartner, Karsten Nysom, Pascal Johann, Kornelius Kerl, Martin Ebinger, David Sumerauer, Stefan Holm, Irene Schmid, Rolf-Dieter Kortmann, Palma Solano-Paez, Susanne Bens, Marcel Kool, N Graf
Publikováno v:
Neuro Oncol
Background Controversy exists as to what may be defined as standard of care (including markers for stratification) for patients with atypical teratoid/rhabdoid tumors (ATRTs). The European Rhabdoid Registry (EU-RHAB) recruits uniformly treated patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89fc297cdaf8a5b3ca41a226fb1d4895
https://www.ncbi.nlm.nih.gov/pubmed/31883020
https://www.ncbi.nlm.nih.gov/pubmed/31883020
Autor:
Domnita O Badarau, Bernice Simone Elger, Pierluigi Brazzola, Heinz Hengartner, Tenzin Wangmo, Katharina M. Ruhe
Publikováno v:
Psycho-Oncology. 25:1036-1042
Objective The aim of the present study is to explore patient's perspectives in pediatric oncology on participation in discussions and decision-making surrounding their cancer diagnosis. Methods Seventeen patients between 9 and 17 years of age receivi