Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jessica I. Hoell"'
Autor:
Thomas Keller, Hannah L. Weber, Jessica I. Hoell, Michaela Kuhlen, Gabriele Gagnon, Laura Trocan, Stefan Balzer, Jens Warfsmann, Mareike Danneberg, G. Janßen
Publikováno v:
European Journal of Pediatrics. 178:1893-1902
Life-limiting conditions in children in specialized pediatric palliative care (PPC) are manifold. The "Together for Short Lives" (TfSL) association established four disease categories, which represent the most common illness trajectories. Better unde
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:
Michaela Kuhlen, G. Janßen, Jens Warfsmann, Jessica I. Hoell, Felix Distelmaier, Arndt Borkhardt
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-7 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Our objective was to evaluate children with metabolic diseases in paediatric palliative home care (PPC) and the process of decision-making. This study was conducted as single-centre retrospective cohort study of patients in the care of a l
Autor:
Hannah L. Weber, Mareike Danneberg, Michaela Kuhlen, G. Janßen, Jessica I. Hoell, Laura Trocan, Arndt Borkhardt, Gabriele Gagnon, Stefan Balzer
Publikováno v:
Oncotarget
// Jessica I. Hoell 1 , Hannah L. Weber 1 , Stefan Balzer 1 , Mareike Danneberg 1 , Gabriele Gagnon 1 , Laura Trocan 1 , Arndt Borkhardt 1 , Gisela Jansen 1 and Michaela Kuhlen 1 1 University of Duesseldorf, Medical Faculty, Department of Pediatric O
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:
Michaela Kuhlen, Florian Babor, Daniel Hein, Salih Demir, Andreas Kloetgen, Ute Fischer, Cornelia Eckert, Jean-Pierre Bourquin, Arndt Borkhardt, Arend von Stackelberg, Ralf Thiele, Martin Schrappe, Anja Moericke, Alice C. McHardy, Christina Peters, Brigitte Strahm, Stefan Krause, Martin Stanulla, Lüder Hinrich Meyer, Jessica I. Hoell, Gabriele Escherich, Peter Bader, Beat Bornhauser, Juergen Enczmann, Julia Alten, Roland Meisel, Friedhelm R. Schuster, Sebastian Ginzel, Michael Gombert, Udo zur Stadt
Publikováno v:
Blood advances
Survival of patients with pediatric acute lymphoblastic leukemia (ALL) after allogeneic hematopoietic stem cell transplantation (allo-SCT) is mainly compromised by leukemia relapse, carrying dismal prognosis. As novel individualized therapeutic appro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bd69364d17cee698258dac0d854488b
Publikováno v:
European Journal of Paediatric Neurology. 20:261-269
Brain tumors have the highest disease-related mortality rate of all pediatric cancers. The goal of this study was to determine whether all children with incurable brain tumors cared for by a pediatric palliative care team in a home setting suffer fro
Autor:
Jessica I. Hoell, Jens Warfsmann, Laura Trocan, Prasad T. Oommen, Arndt Borkhardt, Michaela Kuhlen, G. Janßen, Stefan Balzer, Gabriele Gagnon
Publikováno v:
European journal of pediatrics. 176(10)
The number of children without a diagnosis in pediatric palliative home care and the process of decision-making in these children are widely unknown. The study was conducted as single-center retrospective cohort study. Between January 2013 and Septem
Autor:
Isaac Yaniv, Ulrike Poetschger, Thomas Klingebiel, Michaela Kuhlen, Peter Lang, Martin Schrappe, Jean-Hugues Dalle, Sabina Sufliarska, Petr Sedlacek, Jacek Wachowiak, Evgenia Glogova, Adriana Balduzzi, Irene von Luettichau, Tayfun Guengoer, Brigitte Strahm, Andre Willasch, Arndt Borkhardt, Christina Peters, Jessica I. Hoell, Arend von Stackelberg, Peter Bader, Marianne Ifversen, Roland Meisel
Publikováno v:
British journal of haematology. 180(1)
Relapse remains the major cause of treatment failure in children with high-risk acute lymphoblastic leukaemia (ALL) undergoing allogeneic haematopoietic stem-cell transplantation (allo-SCT). Prognosis is considered dismal but data on risk factors and