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pro vyhledávání: '"Frölich, Saskia"'
Autor:
Ammann-Schnell, Louisa, Groeschel, Samuel, Kehrer, Christiane, Frölich, Saskia, Krägeloh-Mann, Ingeborg
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-16 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-16 (2021)
Background Rare and severe neurological disorders in childhood not only heavily affect the life perspective of the patients, but also their caregivers and families. The aim of this study was to investigate the impact of such diseases on the family, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8be81b0238c9e365567e9aaf9d5fc4f0
http://europepmc.org/articles/PMC8111977
http://europepmc.org/articles/PMC8111977
Autor:
Sánchez-Albisua, Iciar1 iciar.sanchez@med.uni-tuebingen.de, Frölich, Saskia1 saskia.froelich@gmail.com, Barth, Peter G.2 p.g.barth@amc.uva.nl, Steinlin, Maja3 maja.steinlin@insel.ch, Krägeloh-Mann, Ingeborg1 ingeborg.kraegeloh-mann@med.uni-tuebingen.de
Publikováno v:
Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p1-23. 23p.
Autor:
Ekert, Kaspar, Groeschel, Samuel, Sánchez-Albisua, Iciar, Frölich, Saskia, Dieckmann, Andrea, Engel, Corinna, Krägeloh-Mann, Ingeborg
Longitudinal data demonstrating increase in volumes over the first years of life and some volume decrease in one long-term follow-up over 10 years. (PDF 125 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0776809122d647feb7367a08f378ea0e
Autor:
Ekert, Kaspar, Groeschel, Samuel, Sánchez-Albisua, Iciar, Frölich, Saskia, Dieckmann, Andrea, Engel, Corinna, Krägeloh-Mann, Ingeborg
Extracts of scatterplots of figure 2 and 3 of the manuscript over only the first 4 years of life in order to illustrate the early postnatal increase of all brain structures, with the infratentorial structures (A–C) growing to a slower degree compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf9286d252ddd6f92a613d8b7d675b38
Autor:
Frölich, Saskia
Die vorliegende Studie möchte den natürlichen Verlauf der Pontocerebellären Hypoplasie an einer möglichst großen, aber genetisch homogenen, Kohorte näher beschreiben, um neue Erkenntnisse insbesondere über die Entwicklung, das Wachstum und den
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______707::ced9c8d3fed668b1b74092a6c519c191
https://hdl.handle.net/10900/58477
https://hdl.handle.net/10900/58477
Akademický článek
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