Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Ursula G. Froster"'
Autor:
Ralf Porzig, Sina Neugebauer, Thomas Heckmann, Daniela Adolf, Peter Kaskel, Ursula G. Froster
Publikováno v:
BMC Health Services Research, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background Concepts for the nursing and care of cancer patients through a “navigation service” have attracted much interest. However, there is still room for improvement in terms of their funding and coverage. The Saxon Cancer Society de
Externí odkaz:
https://doaj.org/article/f98e9725f19b460eb6044aa4d405fd5b
Autor:
Volker F. H. Brauer, Frank Reichenberger, Anke Müller, Matthias Steinert, Ursula G. Froster, Hubert R. W. Wirtz, Joachim Schauer
Publikováno v:
Sarcoma, Vol 6, Iss 4, Pp 141-143 (2002)
We describe a patient who underwent thoracic radiation therapy for biopsy-proven pulmonary spindle cell sarcoma in the left lower lobe, 15 months after birth. At the age of 37 she developed shoulder pain, fatigue, and progressive exertion dyspnoea. C
Externí odkaz:
https://doaj.org/article/3fce4649b10f47ad9c6b773f6ffcfcf8
Autor:
Sina Neugebauer, Peter Kaskel, Thomas Heckmann, Ursula G. Froster, Daniela Adolf, Ralf Porzig
Publikováno v:
BMC Health Services Research, Vol 18, Iss 1, Pp 1-8 (2018)
Concepts for the nursing and care of cancer patients through a “navigation service” have attracted much interest. However, there is still room for improvement in terms of their funding and coverage. The Saxon Cancer Society designed a prospective
Autor:
Gamze Cömertpay, Ümit Lüleyap, Ayfer Pazarbaşı, Ursula G. Froster, Davut Alptekin, Perçin Pazarcı, Halise Neslihan Önenli, Halil Kasap
Publikováno v:
Volume: 41, Issue: 4 702-708
Cukurova Medical Journal
Cukurova Medical Journal
Amaç: Fenilketonüri, hepatik bir enzim olan fenilalanin hidroksilazın otozomal resesif bozukluğu sonucu ortaya çıkan bir durumdur. Bu çalışmada, Türk popülasyonunda en sık görülen fenilalanin hidroksilaz geni mutasyonlarını belirlemek
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe1e885188c8583a80c14991e0f84d0
https://dergipark.org.tr/tr/pub/cumj/issue/23861/254199
https://dergipark.org.tr/tr/pub/cumj/issue/23861/254199
Publikováno v:
Journal of Chromatographic Science. 48:55-58
Expansion of an unstable trinucleotide (CAG)(n) repeat region within exon 1 of the gene IT15 causes autosomal, dominantly inherited Huntington's disease (HD). The number of CAG-repeats varies from 6 to 35 in normal individuals, whereas in affected pa
Autor:
Markus Loeffler, Monika Graeser, Carolin Nestle-Kraemling, Mohammad Zaino, Marion Kiechle, Sabine Preisler-Adams, Karin Kast, Dorothea Gadzicki, Norbert Arnold, Christoph Engel, Astrid Bechtold, Ursula G. Froster, Rita K. Schmutzler, Dominic Varga, Alfons Meindl, Ulrich Bick, B. Schlehe, Kerstin Rhiem
Publikováno v:
Journal of Clinical Oncology. 27:5887-5892
Purpose To estimate the risk for contralateral breast cancer in members of BRCA1- and BRCA2-positive families and to determine predictive risk factors. Patients and Methods A retrospective, multicenter, cohort study was performed from 1996 until 2008
Autor:
Ignacio Blanco, Heli Nevanlinna, Norbert Arnold, Gad Rennert, Catherine Noguès, Javier Benitez, Etienne Rouleau, Embrace, Gemo, Irene Konstantopoulou, David J. Hughes, Flavio Lejbkowicz, kConFab, Rita K. Schmutzler, Mercedes Durán, Carole Brewer, Beatrix Versmold, Georgia Chenevix-Trench, Paolo Radice, Trevor Cole, Alfons Meindl, Ivan Bièche, Rosalind A. Eeles, Isabelle Coupier, Olga M. Sinilnikova, Hebon, A L Laborde, Florence Coulet, Kristiina Aittomäki, M. Cook, Ana Osorio, D. G. Evans, Dieter Schaefer, S. Giraud, Craig Luccarini, Jacques Simard, Hans J. J. P. Gille, Fiona Lalloo, Liliane Demange, Xiaoqing Chen, Florent Soubrier, Susan Peock, Amanda B. Spurdle, Rosemarie Davidson, Lesley McGuffog, T. A. M. van Os, Henry T. Lynch, Jacqueline Cook, Ursula G. Froster, Douglas F. Easton, Sara Dishon, Siranoush Manoukian, Christian Sutter, Gabriella Pichert, Frans B. L. Hogervorst, Mélanie Léoné, Jonathan Beesley, Katherine L. Nathanson, Rosette Lidereau, Sue Healey, Daniel Sinnett, Gc-Hboc, Christoph Engel, Joan Paterson, Chrystelle Colas, Mark H. Greene, U Hamann, Dominique Stoppa-Lyonnet, Ocgn, Irene L. Andrulis, Helmut Deissler, Jennifer T. Loud, A C Antoniou, Susan M. Domchek
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
BRITISH JOURNAL OF CANCER
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Recercat. Dipósit de la Recerca de Catalunya
British Journal of Cancer
Sinilnikova, O M, Antoniou, A C, Simard, J, Healey, S, Leone, M, Sinnett, D, Spurdle, A B, Beesley, J, Chen, X, Greene, M H, Loud, J T, Lejbkowicz, F, Rennert, G, Dishon, S, Andrulis, I L, Domchek, S M, Nathanson, K L, Manoukian, S, Radice, P, Konstantopoulou, I, Blanco, I, Laborde, A L, Duran, M, Osorio, A, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A M, Gille, J J P, Peock, S, Cook, M, Luccarini, C, Evans, D G, Lalloo, F, Eeles, R, Pichert, G, Davidson, R, Cole, T, Cook, J, Paterson, J, Brewer, C, Hughes, D J, Coupier, I, Giraud, S, Coulet, F, Colas, C, Soubrier, F, Rouleau, E, Bieche, I, Lidereau, R, Demange, L, Nogues, C, Lynch, H T, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Arnold, N, Sutter, C, Deissler, H, Schaefer, D, Froster, U G, Aittomaki, K, Nevanlinna, H, McGuffog, L, Easton, D F, Chenevix-Trench, G & Stoppa-Lyonnet, D 2009, ' The TP53 Arg72Pro and MDM2 309G > T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers ', British Journal of Cancer, vol. 101, no. 8, pp. 1456-1460 . https://doi.org/10.1038/sj.bjc.6605279
British Journal of Cancer, 101(8), 1456-1460. Nature Publishing Group
Universidad de Barcelona
BRITISH JOURNAL OF CANCER
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Recercat. Dipósit de la Recerca de Catalunya
British Journal of Cancer
Sinilnikova, O M, Antoniou, A C, Simard, J, Healey, S, Leone, M, Sinnett, D, Spurdle, A B, Beesley, J, Chen, X, Greene, M H, Loud, J T, Lejbkowicz, F, Rennert, G, Dishon, S, Andrulis, I L, Domchek, S M, Nathanson, K L, Manoukian, S, Radice, P, Konstantopoulou, I, Blanco, I, Laborde, A L, Duran, M, Osorio, A, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A M, Gille, J J P, Peock, S, Cook, M, Luccarini, C, Evans, D G, Lalloo, F, Eeles, R, Pichert, G, Davidson, R, Cole, T, Cook, J, Paterson, J, Brewer, C, Hughes, D J, Coupier, I, Giraud, S, Coulet, F, Colas, C, Soubrier, F, Rouleau, E, Bieche, I, Lidereau, R, Demange, L, Nogues, C, Lynch, H T, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Arnold, N, Sutter, C, Deissler, H, Schaefer, D, Froster, U G, Aittomaki, K, Nevanlinna, H, McGuffog, L, Easton, D F, Chenevix-Trench, G & Stoppa-Lyonnet, D 2009, ' The TP53 Arg72Pro and MDM2 309G > T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers ', British Journal of Cancer, vol. 101, no. 8, pp. 1456-1460 . https://doi.org/10.1038/sj.bjc.6605279
British Journal of Cancer, 101(8), 1456-1460. Nature Publishing Group
BACKGROUND: The TP53 pathway, in which TP53 and its negative regulator MDM2 are the central elements, has an important role in carcinogenesis, particularly in BRCA1- and BRCA2-mediated carcinogenesis. A single nucleotide polymorphism (SNP) in the pro
Publikováno v:
Fetal Diagnosis and Therapy. 26:219-222
We report on partial duplication 21q resulting from a paternal insertion identified during prenatal diagnosis. While performing interphase fluorescence in situ hybridization (I-FISH), we were able to identify 3 signals of the LSI 21 Spectrum Orange p
Autor:
Heli Nevanlinna, Carol Anne Gardiner, Alan Donaldson, Philippe Vennin, Michel Longy, Claude Adenis, Gemo, Timothy R. Rebbeck, Karin Kast, Amanda B. Spurdle, Jacques Simard, Allison M. Male, Jean-Pierre Fricker, Antonis C. Antoniou, Dominique Stoppa-Lyonnet, Virginia G. Kaklamani, kConFab, Ursula G. Froster, Rita K. Schmutzler, Fergus J. Couch, Lucy Side, Boris Pasche, Embrace, Ute Hamann, Jean-Philippe Peyrat, Christoph Engel, Beatrix Versmold, Danièle Muller, Irene L. Andrulis, Susan Peock, Dieter Schaefer, J. Fournier, Ian O. Ellis, Mark H. Greene, Csilla Szabo, Georgia Chenevix-Trench, Margaret Cook, Trinidad Caldés Llopis, Anne C. Robinson, Kristiina Aittomäki, Alfons Meindl, Olga M. Sinilnikova, Helen Gregory, Lutecia Pereira, Douglas F. Easton, Patricia Harrington, Louise Emmerson
Publikováno v:
Breast Cancer Research and Treatment. 115:185-192
BACKGROUND: The transforming growth factor beta-1 gene (TGFB1) is a plausible candidate for breast cancer susceptibility. The L10P variant of TGFB1 is associated with higher circulating levels and secretion of TGF-beta, and recent large-scale studies
Autor:
Claudia Gruenauer-Kloevekorn, Ursula G. Froster, G.I.W Duncker, Saskia Braeutigam, Wolfram Heinritz
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 246:1441-1447
The objective of this study was to investigate genotype-phenotype correlations, the consequences for surgical treatment, and the therapeutical options in patients with macular corneal dystrophy (MCD). We investigated MCD genotype by using polymerase