Zobrazeno 1 - 8
of 8
pro vyhledávání: '"C R M, Lammens"'
Publikováno v:
Spelten, E R, Lammens, C R M, Engelen, V & Duijts, S F A 2020, ' An inventory of psychosocial oncological interventions in The Netherlands: identifying availability, gaps, and overlap in care provision ', Journal of Psychosocial Oncology, vol. 38, no. 1, pp. 36-62 . https://doi.org/10.1080/07347332.2019.1626965
Journal of psychosocial oncology, 38(1), 36-62. ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
Journal of Psychosocial Oncology, 38(1), 36-62. Routledge
Journal of psychosocial oncology, 38(1), 36-62. ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
Journal of Psychosocial Oncology, 38(1), 36-62. Routledge
Purpose: While a wide range of psychosocial oncological (PO) interventions has been developed, a systematic overview of interventions to inform patients, care providers, as well as researchers, policy makers and health insurers, is lacking. The aims
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56355ab5734bd1b8a15aa5bd088baf1e
https://research.vumc.nl/en/publications/3edb9cd4-8a04-452b-9799-5b836124fb92
https://research.vumc.nl/en/publications/3edb9cd4-8a04-452b-9799-5b836124fb92
Autor:
Danielle Majoor-Krakauer, S. Verhoef, Frederik J. Hes, Marielle W. G. Ruijs, T. A. M. van Os, Neil K. Aaronson, Rolf H. Sijmons, Liesbeth Spruijt, C. R. M. Lammens, E. M. A. Bleiker, Tanja Nagtegaal, Margreet G. E. M. Ausems, Encarna B. Gomez-Garcia, A. M. W. Van Den Ouweland, R. B. van der Luijt, Chad M. Gundy
Publikováno v:
Psycho-Oncology. 20:631-638
Objective: Li Fraumeni syndrome (LFS) and Von Hippel-Lindau disease (VHL) are two rare hereditary tumor syndromes, characterized by a high risk of developing multiple tumors at various sites and ages for which preventive and treatment options are lim
Autor:
Senno Verhoef, Tanja Nagtegaal, Liesbeth Spruijt, C. R. M. Lammens, Rolf H. Sijmons, Annette H. J. T. Vriends, Eveline M. A. Bleiker, Irma Kluijt, Margreet G. E. M. Ausems, Marielle W. G. Ruijs, Encarna B. Gomez Garcia, Neil K. Aaronson, Theo A. M. van Os, Anja Wagner
Publikováno v:
Lammens, C R M, Aaronson, N K, Wagner, A, Sijmons, RH, Ausems, M G E M, Vriends, A H J T, Ruijs, M W G, van Os, T A M, Spruijt, L, Garcia, E B G, Kluijt, I, Nagtegaal, T, Verhoef, S & Bleiker, E M A 2010, ' Genetic Testing in Li-Fraumeni Syndrome: Uptake and Psychosocial Consequences ', Journal of Clinical Oncology, vol. 28, no. 18, pp. 3008-3014 . https://doi.org/10.1200/JCO.2009.27.2112
Journal of Clinical Oncology, 28(18), 3008-3014. American Society of Clinical Oncology
Journal of clinical oncology, 28(18), 3008-3014. American Society of Clinical Oncology
Journal of Clinical Oncology, 28(18), 3008-3014
Journal of Clinical Oncology, 28(18), 3008-3014. AMER SOC CLINICAL ONCOLOGY
Journal of Clinical Oncology, 28, 3008-14
Journal of Clinical Oncology, 28, 18, pp. 3008-14
Journal of Clinical Oncology, 28(18), 3008-3014. American Society of Clinical Oncology
Journal of clinical oncology, 28(18), 3008-3014. American Society of Clinical Oncology
Journal of Clinical Oncology, 28(18), 3008-3014
Journal of Clinical Oncology, 28(18), 3008-3014. AMER SOC CLINICAL ONCOLOGY
Journal of Clinical Oncology, 28, 3008-14
Journal of Clinical Oncology, 28, 18, pp. 3008-14
Purpose Li-Fraumeni syndrome (LFS) is a hereditary cancer syndrome, characterized by a high risk of developing cancer at various sites and ages. To date, limited clinical benefits of genetic testing for LFS have been demonstrated, and there are conce
Autor:
Marielle W. G. Ruijs, Margreet G. E. M. Ausems, T. A. M. van Os, Tanja Nagtegaal, Neil K. Aaronson, Annemieke Cats, Annette H. J. T. Vriends, Senno Verhoef, Rolf H. Sijmons, C. R. M. Lammens, E. M. A. Bleiker, Anja Wagner, Liesbeth Spruijt, E. B. Gomez Garcia
Publikováno v:
Familial Cancer, 9(4), 647-654
Familial Cancer, 9(4), 647-654. Springer Netherlands
Familial Cancer, 9, 4, pp. 647-54
Familial Cancer, 9(4), 647-654. SPRINGER
Familial Cancer, 9(4), 647-654. Springer, Cham
Familial Cancer, 9, 647-54
Lammens, C R M, Bleiker, E M A, Aaronson, N K, Wagner, A, Sijmons, RH, Ausems, M G E M, Vriends, A H J T, Ruijs, M W G, van Os, T A M, Spruijt, L, Garcia, E B G, Cats, A, Nagtegaal, T & Verhoef, S 2010, ' Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits ', Familial Cancer, vol. 9, no. 4, pp. 647-654 . https://doi.org/10.1007/s10689-010-9368-z
Familial Cancer
Familial cancer, 9(4), 647-654. Springer Netherlands
Familial Cancer, 9(4), 647-654. Springer Netherlands
Familial Cancer, 9, 4, pp. 647-54
Familial Cancer, 9(4), 647-654. SPRINGER
Familial Cancer, 9(4), 647-654. Springer, Cham
Familial Cancer, 9, 647-54
Lammens, C R M, Bleiker, E M A, Aaronson, N K, Wagner, A, Sijmons, RH, Ausems, M G E M, Vriends, A H J T, Ruijs, M W G, van Os, T A M, Spruijt, L, Garcia, E B G, Cats, A, Nagtegaal, T & Verhoef, S 2010, ' Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits ', Familial Cancer, vol. 9, no. 4, pp. 647-654 . https://doi.org/10.1007/s10689-010-9368-z
Familial Cancer
Familial cancer, 9(4), 647-654. Springer Netherlands
Contains fulltext : 89461.pdf (Publisher’s version ) (Closed access) Li Fraumeni Syndrome (LFS) is a hereditary cancer syndrome characterized by a high risk of developing various types of cancer from birth through late adulthood. Clinical benefits
Autor:
Senno Verhoef, Neil K. Aaronson, Bernard A. Zonnenberg, Liselot P. van Hest, Danielle Majoor-Krakauer, Frederik J. Hes, Rob B. van der Luijt, Jacques W.M. Lenders, Theo A. Mvan Os, Ans M.W. van den Ouweland, Thera P. Links, Encarna B. Gomez-Garcia, C. R. M. Lammens, Eveline M. A. Bleiker, Wouter W. de Herder
Publikováno v:
Genetics in Medicine, 13(6), 519-527. Nature Publishing Group
Genetics in medicine, 13(6), 519-527. Lippincott Williams and Wilkins
Genetics in Medicine, 13(6), 519-527. Lippincott Williams & Wilkins
Genetics in Medicine, 13(6), 519-527. Lippincott Williams and Wilkins
Lammens, C R M, Aaronson, N K, Hes, F J, Links, T P, Zonnenberg, B A, Lenders, J W M, Majoor-Krakauer, D, van Os, T A M, Gomez-Garcia, E B, de Herder, W, van der Luijt, R B, van den Ouweland, A M W, van Hest, L P, Verhoef, S & Bleiker, E M A 2011, ' Compliance with periodic surveillance for Von-Hippel-Lindau disease ', Genetics in Medicine, vol. 13, no. 6, pp. 519-527 . https://doi.org/10.1097/GIM.0b013e3182091a1d
Genetics in Medicine, 13, 6, pp. 519-27
Genetics in Medicine, 13, 519-27
Genetics in medicine, 13(6), 519-527. Lippincott Williams and Wilkins
Genetics in Medicine, 13(6), 519-527. Lippincott Williams & Wilkins
Genetics in Medicine, 13(6), 519-527. Lippincott Williams and Wilkins
Lammens, C R M, Aaronson, N K, Hes, F J, Links, T P, Zonnenberg, B A, Lenders, J W M, Majoor-Krakauer, D, van Os, T A M, Gomez-Garcia, E B, de Herder, W, van der Luijt, R B, van den Ouweland, A M W, van Hest, L P, Verhoef, S & Bleiker, E M A 2011, ' Compliance with periodic surveillance for Von-Hippel-Lindau disease ', Genetics in Medicine, vol. 13, no. 6, pp. 519-527 . https://doi.org/10.1097/GIM.0b013e3182091a1d
Genetics in Medicine, 13, 6, pp. 519-27
Genetics in Medicine, 13, 519-27
Purpose: To assess compliance with a periodic surveillance regimen for Von Hippel-Lindau disease. Methods: In this nationwide study, Von Hippel-Lindau disease mutation carriers and those at 50% risk were invited to complete a questionnaire assessing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::804d646dadad03c1b2c337960c0bc581
https://research.rug.nl/en/publications/f4ad3c2f-cb75-4a2f-b37e-87d04fba36d6
https://research.rug.nl/en/publications/f4ad3c2f-cb75-4a2f-b37e-87d04fba36d6
Autor:
C R M, Lammens, E M A, Bleiker, S, Verhoef, M G E M, Ausems, D, Majoor-Krakauer, R H, Sijmons, F J, Hes, E B, Gómez-García, T A M, Van Os, L, Spruijt, R B, van der Luijt, A M W, van den Ouweland, M W G, Ruijs, C, Gundy, T, Nagtegaal, N K, Aaronson
Publikováno v:
Psycho-oncology. 20(6)
Li Fraumeni syndrome (LFS) and Von Hippel-Lindau disease (VHL) are two rare hereditary tumor syndromes, characterized by a high risk of developing multiple tumors at various sites and ages for which preventive and treatment options are limited. For p
Autor:
R. B. van der Luijt, Neil K. Aaronson, Nicoline Hoogerbrugge, Danielle Majoor-Krakauer, Rolf H. Sijmons, E. B. Gomez Garcia, A. M. W. Van Den Ouweland, Frederik J. Hes, S. Verhoef, Chad M. Gundy, C. R. M. Lammens, Charlotte J. Dommering, E. M. A. Bleiker, Margreet G. E. M. Ausems, T. A. M. van Os
Publikováno v:
Clinical Genetics, 77(5), 483-491
Clinical Genetics, 77(5), 483-491. Wiley
Clinical Genetics, 77, 483-91
Clinical genetics, 77(5), 483-491. Wiley-Blackwell
Lammens, C R M, Bleiker, E M A, Verhoef, S, Hes, F J, Ausems, M G E M, Majoor-Krakauer, D, Sijmons, RH, van der Luijt, R B, van den Ouweland, A M W, Van Os, T, Hoogerbrugge, N, Garcia, E B G, Dommering, C J, Gundy, C & Aaronson, N K 2010, ' Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress ', Clinical Genetics, vol. 77, no. 5, pp. 483-491 . https://doi.org/10.1111/j.1399-0004.2009.01333.x
Clinical Genetics, 77(5), 483-491. Wiley-Blackwell
Clinical Genetics, 77(5), 483-491. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 77, 5, pp. 483-91
Clinical Genetics, 77(5), 483-491. Wiley
Clinical Genetics, 77, 483-91
Clinical genetics, 77(5), 483-491. Wiley-Blackwell
Lammens, C R M, Bleiker, E M A, Verhoef, S, Hes, F J, Ausems, M G E M, Majoor-Krakauer, D, Sijmons, RH, van der Luijt, R B, van den Ouweland, A M W, Van Os, T, Hoogerbrugge, N, Garcia, E B G, Dommering, C J, Gundy, C & Aaronson, N K 2010, ' Psychosocial impact of Von Hippel-Lindau disease: levels and sources of distress ', Clinical Genetics, vol. 77, no. 5, pp. 483-491 . https://doi.org/10.1111/j.1399-0004.2009.01333.x
Clinical Genetics, 77(5), 483-491. Wiley-Blackwell
Clinical Genetics, 77(5), 483-491. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 77, 5, pp. 483-91
Contains fulltext : 89552.pdf (Publisher’s version ) (Closed access) Von Hippel-Lindau disease (VHL) is a hereditary tumor susceptibility syndrome, characterized by an increased risk of developing multiple benign and malignant tumors at various sit
Autor:
Eveline M. A. Bleiker, Neil K. Aaronson, Encarna Gomez Garcia, Ans M.W. van den Ouweland, Senno Verhoef, Liesbeth Spruijt, Anja Wagner, Annette H. J. T. Vriends, C. R. M. Lammens, Marielle W. G. Ruijs, Rolf H. Sijmons, Rob B. van der Luijt, Maaike Jansweijer, Margreet G. E. M. Ausems
Publikováno v:
Familial Cancer, 8, 457-64
Familial cancer, 8(4), 457-464. Springer Netherlands
Familial Cancer, 8(4), 457-464. Springer Netherlands
Lammens, C, Bleiker, E, Aaronson, N, Vriends, A, Ausems, M, Jansweijer, M, Wagner, A, Sijmons, R, van den Ouweland, A, van der Luijt, R, Spruijt, L, Garcia, E G, Ruijs, M W G & Verhoef, S 2009, ' Attitude towards pre-implantation genetic diagnosis for hereditary cancer ', Familial Cancer, vol. 8, no. 4, pp. 457-464 . https://doi.org/10.1007/s10689-009-9265-5
Familial Cancer, 8(4), 457-464. SPRINGER
Familial Cancer
Familial Cancer, 8, 4, pp. 457-64
Familial cancer, 8(4), 457-464. Springer Netherlands
Familial Cancer, 8(4), 457-464. Springer Netherlands
Lammens, C, Bleiker, E, Aaronson, N, Vriends, A, Ausems, M, Jansweijer, M, Wagner, A, Sijmons, R, van den Ouweland, A, van der Luijt, R, Spruijt, L, Garcia, E G, Ruijs, M W G & Verhoef, S 2009, ' Attitude towards pre-implantation genetic diagnosis for hereditary cancer ', Familial Cancer, vol. 8, no. 4, pp. 457-464 . https://doi.org/10.1007/s10689-009-9265-5
Familial Cancer, 8(4), 457-464. SPRINGER
Familial Cancer
Familial Cancer, 8, 4, pp. 457-64
Contains fulltext : 80314.pdf (Publisher’s version ) (Closed access) The use of pre-implantation genetic diagnosis (PGD) for hereditary cancer is subject to on-going debate, particularly among professionals. This study evaluates the attitude toward
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffec84b079a41eb998f3835070ab97b6
http://hdl.handle.net/2066/80314
http://hdl.handle.net/2066/80314