Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Theo M. Starink"'
Autor:
Paul C Johannesma, Irma van de Beek, Tijmen J W T van der Wel, Rinze Reinhard, Lawrence Rozendaal, Theo M Starink, Jan Hein T M van Waesberghe, Simon Horenblas, Hans J J P Gille, Marianne A Jonker, Hanne E J Meijers-Heijboer, Pieter E Postmus, Arjan C Houweling, Jeroen R A van Moorselaar
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0212952 (2019)
Birt-Hogg-Dubé syndrome is associated with an increased risk for renal cell carcinoma. Surveillance is recommended, but the optimal imaging method and screening interval remain to be defined. The main aim of our study was to evaluate the outcomes of
Externí odkaz:
https://doaj.org/article/e061467c213648bc94569e95baa4bfc1
Autor:
Irma van de Beek, Iris E. Glykofridis, Michael W. T. Tanck, Monique N. H. Luijten, Theo M. Starink, Jesper A. Balk, Paul C. Johannesma, Eric Hennekam, Maurice J. B. van den Hoff, Quinn D. Gunst, Johan J. P. Gille, Abeltje M. Polstra, Pieter E. Postmus, Maurice A. M. van Steensel, Alex V. Postma, Rob M. F. Wolthuis, Fred H. Menko, Arjan C. Houweling, Quinten Waisfisz
Publikováno v:
van de Beek, I, Glykofridis, I E, Tanck, M W T, Luijten, M N H, Starink, T M, Balk, J A, Johannesma, P C, Hennekam, E, van den Hoff, M J B, Gunst, Q D, Gille, J J P, Polstra, A M, Postmus, P E, van Steensel, M A M, Postma, A V, Wolthuis, R M F, Menko, F H, Houweling, A C & Waisfisz, Q 2023, ' Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene ', Journal of human genetics, vol. 68, no. 4, pp. 273-279 . https://doi.org/10.1038/s10038-022-01113-1
Journal of human genetics. Nature Publishing Group
Journal of human genetics, 68(4), 273-279. Nature Publishing Group
Journal of human genetics. Nature Publishing Group
Journal of human genetics, 68(4), 273-279. Nature Publishing Group
Previously, we reported a series of families presenting with trichodiscomas, inherited in an autosomal dominant pattern. The phenotype was named familial multiple discoid fibromas (FMDF). The genetic cause of FMDF remained unknown so far. Trichodisco
Autor:
Irma, van de Beek, Iris E, Glykofridis, Michael W T, Tanck, Monique N H, Luijten, Theo M, Starink, Jesper A, Balk, Paul C, Johannesma, Eric, Hennekam, Maurice J B, van den Hoff, Quinn D, Gunst, Johan J P, Gille, Abeltje M, Polstra, Pieter E, Postmus, Maurice A M, van Steensel, Alex V, Postma, Rob M F, Wolthuis, Fred H, Menko, Arjan C, Houweling, Quinten, Waisfisz
Publikováno v:
Journal of human genetics.
Previously, we reported a series of families presenting with trichodiscomas, inherited in an autosomal dominant pattern. The phenotype was named familial multiple discoid fibromas (FMDF). The genetic cause of FMDF remained unknown so far. Trichodisco
Autor:
Lieke M C Gijezen, Marigje Vernooij, Herm Martens, Charlene E U Oduber, Charles J M Henquet, Theo M Starink, Martin H Prins, Fred H Menko, Patty J Nelemans, Maurice A M van Steensel
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e99071 (2014)
Birt-Hogg-Dubé syndrome (BHD) is a rare autosomal dominant disorder characterised by the occurrence of benign, mostly facial, skin tumours called fibrofolliculomas, multiple lung cysts, spontaneous pneumothorax and an increased renal cancer risk. Cu
Externí odkaz:
https://doaj.org/article/0442248d0e704b08977c88ccf54d3d75
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 164
This case concerns a girl with geometrically round blisters, mainly on the left arm since 1 month. Histopathologic examination of a skin biopsy showed a necrotic epidermis with subepidermalclefting suggesting thermal damage. Recently, similar thermal
Autor:
R. Jeroen A. van Moorselaar, Rinze Reinhard, Theo M. Starink, Fred H. Menko, Jan-Hein T M van Waesberghe, Johan J.P. Gille, I. van de Beek, Paul C Johannesma, Pieter E. Postmus, Arjan C. Houweling, Erik Thunnissen
Publikováno v:
Familial Cancer
Familial Cancer, 15(2), 297-300. Springer Netherlands
Johannesma, P C, Houweling, A C, Menko, F, van de Beek, I, Reinhard, R, Gille, J J P, van Waesberghe, J, Thunnissen, E, Starink, T M, Postmus, P E & van Moorselaar, R J A 2016, ' Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis? ', Familial Cancer, vol. 15, no. 2, pp. 297-300 . https://doi.org/10.1007/s10689-015-9853-5
Familial cancer, 15(2), 297-300. Springer Netherlands
Familial Cancer, 15(2), 297-300. Springer Netherlands
Johannesma, P C, Houweling, A C, Menko, F, van de Beek, I, Reinhard, R, Gille, J J P, van Waesberghe, J, Thunnissen, E, Starink, T M, Postmus, P E & van Moorselaar, R J A 2016, ' Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis? ', Familial Cancer, vol. 15, no. 2, pp. 297-300 . https://doi.org/10.1007/s10689-015-9853-5
Familial cancer, 15(2), 297-300. Springer Netherlands
Renal cell cancer (RCC) represents 2–3 % of all cancers and is the most lethal of the urologic malignancies, in a minority of cases caused by a genetic predisposition. Birt–Hogg–Dubé syndrome (BHD) is one of the hereditary renal cancer syndrom
Autor:
Elisabeth H Jaspars, N.C.T. van Grieken, M. B. A. van Doorn, Edward M Leter, Ernie M.H.F. Bongers, Paul C Johannesma, Pieter E. Postmus, Lieke Gijezen, J-H T. M. van Waesberghe, Theo M. Starink, M.A.M. van Steensel, Arjan C. Houweling, Rogier A. Oldenburg, R.J.A. Van Moorselaar, Marianne A. Jonker, T. A. M. van Os, Johan J.P. Gille, K. Y. van Spaendonck-Zwarts, M. M. de Jong, Fred H. Menko
Publikováno v:
British Journal of Cancer, 105(12), 1912-1919. Nature Publishing Group
Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A M, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J H T M, Starink, T M, van Steensel, M A M, Gille, J J P & Menko, F H 2011, ' Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families ', British Journal of Cancer, vol. 105, no. 12, pp. 1912-1919 . https://doi.org/10.1038/bjc.2011.463
British Jounal of Cancer, 105(12), 1912-1919. Nature Publishing Group
British Journal of Cancer
British journal of cancer, 105(12), 1912-1919. Nature Publishing Group
Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A M, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J H T M, Starink, T M, van Steensel, M A M, Gille, J J P & Menko, F H 2011, ' Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families ', British Journal of Cancer, vol. 105, no. 12, pp. 1912-1919 . https://doi.org/10.1038/bjc.2011.463
British Jounal of Cancer, 105(12), 1912-1919. Nature Publishing Group
British Journal of Cancer
British journal of cancer, 105(12), 1912-1919. Nature Publishing Group
Background: Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant condition caused by germline FLCN mutations, and characterised by fibrofolliculomas, pneumothorax and renal cancer. The renal cancer risk, cancer phenotype and pneumothorax risk of B
Autor:
Fred H. Menko, Theo M. Starink, Pieter E. Postmus, Jan-Hein T M van Waesberghe, Arjan C. Houweling, Paul C Johannesma, R. Jeroen A. van Moorselaar
Publikováno v:
Respirology. 19:1248-1250
The development and natural course of lung cysts in patients with Birt-Hogg-Dube syndrome (BHD) is still unclear, and the relationship between lung cysts and pneumothorax is not fully clarified. Based on the follow-up results of thoracic imaging in s
Autor:
Edward M Leter, Johan J.P. Gille, Gabriëlle G Vittoz, Elisabeth H Jaspars, Fred H. Menko, Theo M. Starink, Eric F L David, A Karijn Koopmans, Pieter E. Postmus, R. Jeroen A. van Moorselaar, M. E. Craanen, Theo A. M. van Os
Publikováno v:
Journal of investigative dermatology, 128(1), 45-49. Nature Publishing Group
Journal of Investigative Dermatology, 128(1), 45-49. Nature Publishing Group
Leter, E M, Koopmans, A K, Gille, J J P, van Os, T A M, Vittoz, G G, David, E F, Jaspars, E H, Postmus, P E, van Moorselaar, R J A, Craanen, M E, Starink, T M & Menko, F H 2008, ' Birt-Hogg-Dube syndrome: clinical and genetic studies of 20 families ', Journal of Investigative Dermatology, vol. 128, no. 1, pp. 45-49 . https://doi.org/10.1038/sj.jid.5700959
Journal of Investigative Dermatology, 128(1), 45-49. Nature Publishing Group
Leter, E M, Koopmans, A K, Gille, J J P, van Os, T A M, Vittoz, G G, David, E F, Jaspars, E H, Postmus, P E, van Moorselaar, R J A, Craanen, M E, Starink, T M & Menko, F H 2008, ' Birt-Hogg-Dube syndrome: clinical and genetic studies of 20 families ', Journal of Investigative Dermatology, vol. 128, no. 1, pp. 45-49 . https://doi.org/10.1038/sj.jid.5700959
Birt-Hogg-Dubé syndrome (BHD) is an autosomal-dominant genodermatosis characterized by skin fibrofolliculomas and an increased risk of spontaneous pneumothorax, renal and possibly other tumors. A causative gene (FLCN) on chromosome 17p has recently
Autor:
Marjolein Lettink, Theo M. Starink, Maaike C G Bleeker, Chris J.L.M. Meijer, Albertus T. Hesselink, Peter J.F. Snijders, Feja J. Voorhorst, Tom J Stoof, Cornelis J.A. Hogewoning, Adriaan J. C. van den Brule, Johannes Berkhof
Publikováno v:
Bleeker, M C G, Hogewoning, C J A, Voorhorst, F J, van den Brule, A J C, Berkhof, J, Hesselink, A T, Lettink, M, Starink, T M, Stoof, T J, Snijders, P J F & Meijer, C J L M 2005, ' HPV-associated flat penile lesions in men of a non-STD hospital population : less frequent and smaller in size than in male sexual partners of women with CIN ', International Journal of Cancer, vol. 113, no. 1, pp. 36-41 . https://doi.org/10.1002/ijc.20502
International Journal of Cancer, 113(1), 36-41. Wiley-Liss Inc.
International Journal of Cancer, 113(1), 36-41. Wiley-Liss Inc.
Human papillomavirus (HPV) infections and HPV-associated penile lesions are frequently found in male sexual partners of women with cervical intraepithelial neoplasia (CIN). To determine the significance of these findings, we studied the prevalence of