Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jessica I. Hoell"'
Autor:
Jörg Schaper, Arndt Borkhardt, Sebastian Ginzel, Torsten Pietsch, Jessica I. Hoell, Thorsten Rosenbaum, Michaela Kuhlen, Celine Chiu, Stefanie Loth
Publikováno v:
Familial cancer 18(3), 353-358 (2019). doi:10.1007/s10689-019-00121-z
Medulloblastoma is the most frequent malignant brain tumor in childhood. This highly malignant neoplasm occurs usually before 10 years of age and more frequently in boys. The 5-year event-free survival rate for high-risk medulloblastoma is low at 62%
An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome
Autor:
Inbal Kedar, Christi J. van Asperen, Jeanine J. Houwing-Duistermaat, Laurence Brugières, Sergey Nikolaev, Michael Farrell, Anja Wagner, D. Gareth Evans, Lone Sunde, Yael Goldberg, Mar Rodríguez-Girondo, Jessica I. Hoell, Katharina Wimmer, Karl Heinimann, Stefan Aretz, Maartje Nielsen, Heleen M. van der Klift, Maria Grazia Tibiletti, Tim Ripperger, Leigha Senter, Sanne W. ten Broeke, Wenche Sjursen, Encarna B. Gomez-Garcia, Stefanie Y. Zimmermann, Daniel Rueda, Marjolijn C.J. Jongmans, Noémie Lavoine, Ingrid Winship, Christina Therkildsen, Gabriel Capellá Munar, Chrystelle Colas, Alison H. Trainer, Kory Jasperson, Maurizio Genuardi, Theo A. M. van Os, Yvonne J. Vos, Mitul Modi, Hans F. A. Vasen, Manon Suerink
Publikováno v:
Suerink, M, Rodríguez-Girondo, M, van der Klift, H M, Colas, C, Brugieres, L, Lavoine, N, Jongmans, M, Munar, G C, Evans, D G, Farrell, M P, Genuardi, M, Goldberg, Y, Gomez-Garcia, E, Heinimann, K, Hoell, J I, Aretz, S, Jasperson, K W, Kedar, I, Modi, M B, Nikolaev, S, van Os, T A M, Ripperger, T, Rueda, D, Senter, L, Sjursen, W, Sunde, L, Therkildsen, C, Tibiletti, M G, Trainer, A H, Vos, Y J, Wagner, A, Winship, I, Wimmer, K, Zimmermann, S Y, Vasen, H F, van Asperen, C J, Houwing-Duistermaat, J J, Ten Broeke, S W & Nielsen, M 2019, ' An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome ', Genetics in Medicine, vol. 21, no. 12, pp. 2706-2712 . https://doi.org/10.1038/s41436-019-0577-z
Evans, D G & et al. 2019, ' An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0577-z
Genetics in Medicine
Genetics in Medicine, 21, 2706. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Nature Publishing Group
Genetics in medicine. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Lippincott Williams & Wilkins
Genetics in Medicine, 21(12), 2706-2712
Evans, D G & et al. 2019, ' An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0577-z
Genetics in Medicine
Genetics in Medicine, 21, 2706. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Nature Publishing Group
Genetics in medicine. Lippincott Williams and Wilkins
Genetics in Medicine, 21(12), 2706-2712. Lippincott Williams & Wilkins
Genetics in Medicine, 21(12), 2706-2712
Purpose: Biallelic pathogenic variants in the mismatch repair (MMR) genes cause a recessive childhood cancer predisposition syndrome known as constitutional mismatch repair deficiency (CMMRD). Family members with a heterozygous MMR variant have Lynch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77776c64c226d28d2628f88134704b43
https://pure.au.dk/portal/da/publications/an-alternative-approach-to-establishing-unbiased-colorectal-cancer-risk-estimation-in-lynch-syndrome(44d3cbe1-e2d3-43cf-a924-6d04a2831e62).html
https://pure.au.dk/portal/da/publications/an-alternative-approach-to-establishing-unbiased-colorectal-cancer-risk-estimation-in-lynch-syndrome(44d3cbe1-e2d3-43cf-a924-6d04a2831e62).html
Autor:
Triantafyllia Brozou, Olivier Lascols, Michaela Kuhlen, Chrystelle Colas, Julia Taeubner, Christine Fauth, Jessica I. Hoell, Katharina Wimmer, Joerg Felsberg, Jasmin C. Riemer, Sebastian Ginzel, Arndt Borkhardt, Martine Muleris, Michael Gombert
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2018, 26 (3), pp.440-444. ⟨10.1038/s41431-017-0071-5⟩
European Journal of Human Genetics, Nature Publishing Group, 2018, 26 (3), pp.440-444. ⟨10.1038/s41431-017-0071-5⟩
Constitutional mismatch repair deficiency (CMMRD) is an autosomal recessively inherited childhood cancer susceptibility syndrome caused by biallelic germline mutations in one of the mismatch repair (MMR) genes. The spectrum of CMMRD-associated tumour
Autor:
M. Streiter, A. Prokop, Jessica I. Hoell, Sebastian Ginzel, S. Loth, Pablo Landgraf, V. Käfer, Ralf Thiele, Arndt Borkhardt, Michael Gombert, M. Weiss
Publikováno v:
Klinische Padiatrie. 226(6-7)
Background: Cases of children with more than one type of cancer either diagnosed simultaneously or successively, rarely occur in pediatric oncology. A second malignant neoplasm may be caused by mutagenic effects of the treatment of the primary malign
Autor:
Jessica I, Hoell, Michael, Gombert, Christoph, Bartenhagen, Sebastian, Ginzel, Peter, Husemann, Jörg, Felsberg, Guido, Reifenberger, Angelika, Eggert, Martin, Dugas, Stefan, Schönberger, Arndt, Borkhardt, Ute, Fischer
Publikováno v:
Genes, chromosomescancer. 52(10)