Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lillian Bomme Ousager"'
Autor:
Marie Louise Mølgaard Binderup, Søs Marie Luise Bisgaard, Vibeke Harbud, Hans Ulrik Møller, Steen Gimsing, Lennart Jan Friis-Hansen, Thomas van Overeem Hansen, Per Bagi, Ulrich Knigge, Michael Kosteljanetz, Lars Bøgeskov, Carsten Thomsen, Anne-Marie Axø Gerdes, Lillian Bomme Ousager, Lone Sunde
Publikováno v:
Aarhus University
Binderup, M L M, Bisgaard, S M L, Harbud, V, Møller, H U, Gimsing, S, Friis-Hansen, L J, Hansen, T V O, Bagi, P, Knigge, U, Kosteljanetz, M, Bøgeskov, L, Thomsen, C, Gerdes, A-M A, Ousager, L B & Sunde, L 2013, ' Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition ', Danish Medical Journal, vol. 60, no. 12, pp. B4763 .
Binderup, M L M, Bisgaard, S M L, Harbud, V, Møller, H U, Gimsing, S, Friis-Hansen, L J, Hansen, T V O, Bagi, P, Knigge, U, Kosteljanetz, M, Bøgeskov, L, Thomsen, C, Gerdes, A-M A, Ousager, L B & Sunde, L 2013, ' Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition ', Danish Medical Journal, vol. 60, no. 12, pp. B4763 .
These clinical guidelines outline the criteria and recommendations for diagnostic and genetic work-up of families suspected of von Hippel-Lindau disease (vHL), as well as recommendations for prophylactic surveillance for vHL patients. The guideline h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fb5a061663542d6fbeb141cd2dde5472
https://pubmed.ncbi.nlm.nih.gov/24355456
https://pubmed.ncbi.nlm.nih.gov/24355456
Autor:
Jacopo Celli, Marcel A. M. M. Mannens, Maria Paola Lombardi, Michael T. Gabbett, Jasper J. van der Smagt, Lillian Bomme Ousager, Raoul C.M. Hennekam, Saskia Bulk, Maria Soller, Robert Smigiel, Eva-Lena Stattin, AK Lampe
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2011, 32 (7), pp.723. ⟨10.1002/humu.21505⟩
Human mutation, 32(7), 723-728. Wiley-Liss Inc.
Lombardi, M P, Bulk, S, Celli, J, Lampe, A, Gabbett, M T, Ousager, L B, van der Smagt, J J, Soller, M, Stattin, E-L, Mannens, M A M M, Smigiel, R & Hennekam, R C 2011, ' Mutation update for the PORCN gene ', Human Mutation, vol. 32, no. 7, pp. 723-8 . https://doi.org/10.1002/humu.21505
Human Mutation; Vol 32
Human Mutation, Wiley, 2011, 32 (7), pp.723. ⟨10.1002/humu.21505⟩
Human mutation, 32(7), 723-728. Wiley-Liss Inc.
Lombardi, M P, Bulk, S, Celli, J, Lampe, A, Gabbett, M T, Ousager, L B, van der Smagt, J J, Soller, M, Stattin, E-L, Mannens, M A M M, Smigiel, R & Hennekam, R C 2011, ' Mutation update for the PORCN gene ', Human Mutation, vol. 32, no. 7, pp. 723-8 . https://doi.org/10.1002/humu.21505
Human Mutation; Vol 32
International audience; Mutations in the PORCN gene were first identified in Goltz-Gorlin syndrome patients in 2007. Since then several reports have been published describing a large variety of genetic defects resulting in the Goltz-Gorlin syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e86b3508bceb0ceb9f10ff7ebbc17556
https://hal.archives-ouvertes.fr/hal-00654141/file/PEER_stage2_10.1002%2Fhumu.21505.pdf
https://hal.archives-ouvertes.fr/hal-00654141/file/PEER_stage2_10.1002%2Fhumu.21505.pdf
Autor:
Inge Bernstein, Lillian Bomme Ousager, Anders Bojesen, Katrine Urth Hansen, Michael Hardt-Madsen, Lars Henrik Jensen, Lene Byriel, Christian Ladefoged, Jan Lindebjerg, Tine Plato Hansen
Publikováno v:
Web of Science
6600 Background: A myriad of molecular markers has been proposed and tested with the promise of improving cancer care. Few have been validated and even fewer have been implemented in daily clinic. The most common hereditary colorectal cancer entity,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::331ad011a10295f9cd675669fe00dfa4
https://doi.org/10.1200/jco.2013.31.15_suppl.6600
https://doi.org/10.1200/jco.2013.31.15_suppl.6600