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PURPOSE Malignant optic glioma of adulthood is a rare, invasive neoplasm of the anterior visual pathway with 66 cases reported in the literature. It presents as anaplastic astrocytoma (WHO grade III) or glioblastoma (WHO grade IV). The present case s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3266d67a3f25843249a819c98e5515e8
http://doc.rero.ch/record/332505/files/417_2015_Article_3045.pdf
http://doc.rero.ch/record/332505/files/417_2015_Article_3045.pdf
Autor:
Landau K
Publikováno v:
Ergonomics International Journal. 4
Plane deicing is mandatory to insure safe plane take-off. Previous human factors studies have shown that open-basket deicing activity can be improved. The objective of the paper is to compare heart rate assessment models within a field study with num
Autor:
Landau K
Publikováno v:
Ergonomics International Journal. 4
Publikováno v:
J Physiol
Motor unit activity in human eye muscles during the vestibulo-ocular reflex (VOR) is not well understood, since the associated head and eye movements normally preclude single unit recordings. Therefore we recorded single motor unit activity following
Autor:
Landau, K
Publikováno v:
Fallbeispiele Augenheilkunde ISBN: 9783642422188
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd15ef09caeb697da3ce46b16e366093
https://doi.org/10.1007/978-3-642-42219-5_33
https://doi.org/10.1007/978-3-642-42219-5_33
Autor:
Attenhofer, C, Rohrbach, M, Matyas, G, Schönhoff, Florian, Baumgartner, M, Oxenius, D, Carrel, Thierry, Huebler, M, Min, K, De Pasquale, G, Landau, K, Kretschmar, O, Odavic, D, Vogt, P, Faletra, F, Greutmann, M
Publikováno v:
Attenhofer, C; Rohrbach, M; Matyas, G; Schönhoff, Florian; Baumgartner, M; Oxenius, D; Carrel, Thierry; Huebler, M; Min, K; De Pasquale, G; Landau, K; Kretschmar, O; Odavic, D; Vogt, P; Faletra, F; Greutmann, M (2015). Marfan-Syndrom: Wissenswertes zu Diagnose und Therapie für die Praxis. Swiss Medical Forum, 15(29-30), pp. 674-683. EMH Swiss Medical Publishers
• Das M arfan-Syndrom ist die häufigste h ereditäre Bindegewebskrankheit mit einer Häufigkeit (Prävalenz) von etwa 1:5000. • Die Ursache ist eine Mutation im FBN1-Gen. Die Vererbung erfolgt autosomal- dominant, bei etwa 30% der Fälle handelt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ba885475e469636711d4b66a379dff
https://boris.unibe.ch/75672/1/smf-02350.pdf
https://boris.unibe.ch/75672/1/smf-02350.pdf