Zobrazeno 1 - 10
of 274
pro vyhledávání: '"M. M. de Jong"'
Autor:
Cindy M. M. de Jong, Gudula J.A.M. Boon, Y. N. Jenny Le, Stefano Barco, Bob Siegerink, Frederikus A. Klok
Publikováno v:
Seminars in Thrombosis and Hemostasis.
A broad spectrum of long-term sequelae may be present in venous thromboembolism (VTE) survivors, affecting their quality of life and functioning. To monitor recovery and improve the prognosis of patients with persistent functional limitations, the de
Autor:
Adam M Gwozdz, Cindy M M de Jong, Luz Sousa Fialho, Theerawich Likitabhorn, Frieda Sossi, Paula Blancarte Jaber, Anette Arbjerg Højen, Juan I Arcelus, William R Auger, Cihan Ay, Stefano Barco, Marcelo B Gazzana, Julie Bayley, Laurent Bertoletti, Arina ten Cate-Hoek, Alexander T Cohen, Jean M Connors, Jean-Philippe Galanaud, Nicos Labropoulos, Nicole Langlois, Mark H Meissner, Simon Noble, Esther J Nossent, Paula Ponce de León Lovatón, Helia Robert-Ebadi, Rachel P Rosovsky, Noa Smolenaars, Mark Toshner, Cécile Tromeur, Kang-Ling Wang, Eli Westerlund, Kerstin de Wit, Stephen A Black, Frederikus A Klok
Publikováno v:
Gwozdz, A M, de Jong, C M M, Fialho, L S, Likitabhorn, T, Sossi, F, Jaber, P B, Højen, A A, Arcelus, J I, Auger, W R, Ay, C, Barco, S, Gazzana, M B, Bayley, J, Bertoletti, L, Cate-Hoek, A T, Cohen, A T, Connors, J M, Galanaud, J-P, Labropoulos, N, Langlois, N, Meissner, M H, Noble, S, Nossent, E J, de León Lovatón, P P, Robert-Ebadi, H, Rosovsky, R P, Smolenaars, N, Toshner, M, Tromeur, C C, Wang, K-L, Westerlund, E, de Wit, K, Black, S A & Klok, F A 2022, ' Development of an international standard set of outcome measures for patients with venous thromboembolism : an International Consortium for Health Outcomes Measurement consensus recommendation ', The Lancet Haematology, vol. 9, no. 9, pp. e698-e706 . https://doi.org/10.1016/S2352-3026(22)00215-0
Gwozdz, A M, de Jong, C M M, Fialho, L S, Likitabhorn, T, Sossi, F, Jaber, P B, Højen, A A, Arcelus, J I, Auger, W R, Ay, C, Barco, S, Gazzana, M B, Bayley, J, Bertoletti, L, Cate-Hoek, A T, Cohen, A T, Connors, J M, Galanaud, J P, Labropoulos, N, Langlois, N, Meissner, M H, Noble, S, Nossent, E J, de León Lovatón, P P, Robert-Ebadi, H, Rosovsky, R P, Smolenaars, N, Toshner, M, Tromeur, C, Wang, K L, Westerlund, E, de Wit, K, Black, S A & Klok, F A 2022, ' Development of an international standard set of outcome measures for patients with venous thromboembolism : an International Consortium for Health Outcomes Measurement consensus recommendation ', The Lancet Haematology, vol. 9, no. 9, pp. e698-e706 . https://doi.org/10.1016/S2352-3026(22)00215-0
The Lancet Haematology, 9(9), E698-E706. ELSEVIER SCI LTD
Gwozdz, A M, de Jong, C M M, Fialho, L S, Likitabhorn, T, Sossi, F, Jaber, P B, Højen, A A, Arcelus, J I, Auger, W R, Ay, C, Barco, S, Gazzana, M B, Bayley, J, Bertoletti, L, Cate-Hoek, A T, Cohen, A T, Connors, J M, Galanaud, J P, Labropoulos, N, Langlois, N, Meissner, M H, Noble, S, Nossent, E J, de León Lovatón, P P, Robert-Ebadi, H, Rosovsky, R P, Smolenaars, N, Toshner, M, Tromeur, C, Wang, K L, Westerlund, E, de Wit, K, Black, S A & Klok, F A 2022, ' Development of an international standard set of outcome measures for patients with venous thromboembolism : an International Consortium for Health Outcomes Measurement consensus recommendation ', The Lancet Haematology, vol. 9, no. 9, pp. e698-e706 . https://doi.org/10.1016/S2352-3026(22)00215-0
The Lancet Haematology, 9(9), E698-E706. ELSEVIER SCI LTD
The International Consortium for Health Outcomes Measurement assembled an international working group of venous thromboembolism experts and patient representatives to develop a standardised minimum set of outcomes and outcome measurements for integra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b7f5b38e35e1833ca2a3b98a8746d41
https://www.repository.cam.ac.uk/handle/1810/344391
https://www.repository.cam.ac.uk/handle/1810/344391
Autor:
S R Offerman, Marieke H A Lammertink, W. H. de Vos tot Nederveen Cappel, H. L. van Westreenen, Hans F. A. Vasen, M M de Jong, J.W.B. de Groot, Laura W. Leicher, Hans Morreau
Publikováno v:
Scandinavian Journal of Gastroenterology, 53(5), 632-636
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 53(5), 632-636. Taylor & Francis Group
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 53(5), 632-636. Taylor & Francis Group
Introduction: Mismatch repair deficiency (dMMR) can be found in Lynch syndrome (LS)-associated colorectal carcinoma and in 15% of sporadic colorectal cancer (CRC). Outcome of MMR-deficiency testing is important for surgical decisions as extended cole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37d69dca148354f77b8cd37f98957731
http://hdl.handle.net/1887/95476
http://hdl.handle.net/1887/95476
Autor:
Hendrika Boezen, M M de Jong, W.T.A. van der Graaf, Jelle Wesseling, Michael Schaapveld, Hermien Hartog
Publikováno v:
Breast, 22, 1155-60
Breast, 22, 6, pp. 1155-60
The Breast, 22(6), 1155-1160. Churchill Livingstone
Breast, 22, 6, pp. 1155-60
The Breast, 22(6), 1155-1160. Churchill Livingstone
Item does not contain fulltext High circulating insulin-like growth factor 1 (IGF-1) levels are firmly established as a risk factor for developing breast cancer, especially estrogen positive tumors. The effect of circulating IGF-1 on prognosis once a
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:
S. Kitsiou Tzeli, Hülya Kayserili, L. Giordano, B. Rodriguez, P. Collignon, V. Sabolic Avramovska, Silvana Briuglia, Christopher A. Walsh, Laila Bastaki, Amy Goldstein, Francesca Faravelli, F. Papadia, A. Permunian, Alessandro Simonati, S. Halldorsson, Gian Marco Ghiggeri, David G. Brooks, Clara Barbot, Kathryn J. Swoboda, Chiara Pantaleoni, O. D'Addato, Jason W. Caldwell, Maria Roberta Cilio, Soumaya Mougou-Zerelli, M. Vascotto, Andreas Zankl, Gaetano Tortorella, Julia Tantau, Elliott H. Sherr, Patrizia Accorsi, Maurizio Genuardi, Carmelo Salpietro, G. Marra, Pierangela Castorina, Petter Strømme, J. Johannsdottir, Bruno Dallapiccola, Kenton R. Holden, Donatella Greco, Maria Spanò, Pasquale Parisi, Roberta Battini, Paola Grammatico, P. Ludvigsson, Dorit Lev, Daria Riva, C. Ae Kim, WB Dobyns, L. Martorell Sampol, Robert P. Cruse, H. Raynes, Sabrina Signorini, A. Seward, Raoul C.M. Hennekam, Elena Andreucci, Manuela Priolo, Banu Anlar, Bernard Stuart, Christopher P. Bennett, S. Comu, Christopher Geoffrey Woods, Vlatka Mejaški-Bošnjak, J. Milisa, Eamonn Sheridan, Melissa Lees, C. Moco, Ender Karaca, Miriam Iannicelli, Annalisa Mazzotta, C. Dacou-Voutetakis, Tania Attié-Bitach, Philippe Loget, D. Petkovic, L. Demerleir, Loredana Boccone, Meriem Tazir, Kalpathy S. Krishnamoorthy, Damir Lončarević, Dominika Swistun, Yves Sznajer, Stefano D'Arrigo, Ginevra Zanni, Angela Barnicoat, Marina Michelson, L. I. Al Gazali, Vincenzo Leuzzi, G. Uziel, A. Adami, B. Gener Querol, V. Udani, M. Di Giacomo, Maryse Bonnière, Enrico Bertini, K. Dias, Edward Blair, Johannes M. Penzien, M. Cazzagon, Susana Quijano-Roy, Trine Prescott, Barbara Scelsa, Giuseppina Vitiello, Francesco Brancati, Gilda Stringini, Trudy McKanna, Roser Pons, Renato Borgatti, M. Gentile, Dean Sarco, C. Von Der Lippe, Eugen Boltshauser, Luigina Spaccini, A. Pessagno, Alex Magee, Marilena Briguglio, Margherita Silengo, Lena Starck, M. L. Di Sabato, Roshan Koul, Nicole I. Wolf, A. M. Laverda, Elizabeth Flori, Clotilde Lagier-Tourenne, A. Matuleviciene, Matloob Azam, Kathrin Ludwig, Ghada M H Abdel-Salam, Atıl Yüksel, Johannes R. Lemke, Stefania Bigoni, Elizabeth Said, Anna Rajab, Mary Kay Koenig, Andreas R. Janecke, Asma A. Al-Tawari, Agnese Suppiej, Henry Sanchez, Wendy K. Chung, P. Guanciali, Heike Philippi, Silvia Majore, E. DeMarco, J. Hahn, Gianluca Caridi, Marc D'Hooghe, M. M. De Jong, M. Akcakus, Franco Stanzial, Silvia Battaglia, Gian Luigi Ardissino, Giangennaro Coppola, Jane A. Hurst, Terry D. Sanger, Alessandra Renieri, Nadia Elkhartoufi, Rita Fischetto, Alex E. Clark, S. Strozzi, S. Romano, Alain Verloes, Marzia Pollazzon, Elisa Fazzi, L. Yates, Faustina Lalatta, Sabine Sigaudy, Alessandra D'Amico, Brigitte Leroy, Joel Victor Fluss, David Viskochil, Alice Abdel-Aleem, Darryl C. De Vivo, Padraic Grattan-Smith, Corrado Romano, D. Nicholl, Regine Schubert, A. Moreira, Claudia Izzi, Barbara Gentilin, Gustavo Maegawa, Céline Gomes, László Sztriha, C. Donahue, Luciana Rigoli, Jean Messer, Sophie Thomas, E. Del Giudice, R. Van Coster, André Mégarbané, Ignacio Pascual-Castroviejo, Alessandra Ferlini, Topcu, R. Touraine, Ginevra Guanti, Lorena Travaglini, L. Ali Pacha, R. De Vescovi, Enza Maria Valente, Filippo Bernardi, L. Carr, Shubha R. Phadke, S. Bernes, Maria Teresa Divizia, C. Daugherty, M. Akgul, C. Macaluso, Maha S. Zaki, E. Finsecke, Itxaso Marti, Lorenzo Pinelli, F. McKay, Maria Amorini, Joseph G. Gleeson, F. Benedicenti, Bruria Ben-Zeev, Carla Uggetti, R. Romoli, Richard J. Leventer, Francesco Emma, T. E. Gallager, P. De Lonlay, Marco Seri, Bernard L. Maria, M.A. Donati, Bosanka Jocic-Jakubi
Publikováno v:
International JSRD Study Group 2010, ' Novel TMEM67 mutations and genotype-phenotype correlates in meckelin-related ciliopathies ', Human Mutation, vol. 31, no. 5, pp. E1319-E1331 . https://doi.org/10.1002/humu.21239
Human Mutation, 31(5), E1319-E1331. Wiley-Liss Inc.
Human Mutation, 31(5), E1319-E1331. Wiley-Liss Inc.
Human ciliopathies are hereditary conditions caused by defects of proteins expressed at the primary cilium. Among ciliopathies, Joubert syndrome and related disorders (JSRD), Meckel syndrome (MKS) and nephronophthisis (NPH) present clinical and genet
Autor:
G. J. Te Meerman, W.T.A. van der Graaf, M M de Jong, R. M. W. Hofstra, Marcel Bruinenberg, Michael Schaapveld, Ilja M. Nolte, Jan H. Kleibeuker, E.G.E. de Vries, G van der Steege, Rolf H. Sijmons, Marcel Mulder
Publikováno v:
Digestive and Liver Disease, 36(12), 821-823. ELSEVIER SCIENCE INC
Background and aims. In one small study, the DCC Arg201Gly polymorphism has been observed more frequently in colorectal cancer cases compared with controls. We wondered whether these results could be replicated in a much larger study.Methodology. The
Autor:
M. M. de Jong, A. Mohan, J. K. Rath, R. E. I. Schropp, Vladimir Yu. Nosenko, Padma K. Shukla, Markus H. Thoma, Hubertus M. Thomas
Publikováno v:
AIP Conference Proceedings.
Using an energy resolved mass spectrometer we measured the ion energy and abundance of SinH2n+1+(n = 1…5) ions reaching the growing surface as a function of temperature and pressure in a very high frequency (VHF) hydrogen diluted silane plasma. We
Autor:
S. Halldorsson, Elliott H. Sherr, Susana Quijano-Roy, Gaetano Tortorella, Marc D'Hooghe, M. M. De Jong, J. Caldwell, Gian M. Ghiggeri, Josseline Kaplan, Christopher P. Bennett, S. Comu, Vincenzo Leuzzi, Anna Rajab, Mary Kay Koenig, Serap Teber, Barbara Scelsa, G. Marra, S. Kitsiou Tzeli, D. Petkovic, Alex E. Clark, Bruno Dallapiccola, P. Collignon, V. Sabolic Avramovska, Richard J. Leventer, Robert P. Cruse, Sabrina Signorini, Raoul C.M. Hennekam, Nicole I. Wolf, A. M. Laverda, Brunella Mancuso, Clotilde Lagier-Tourenne, Kathrin Ludwig, C. Moco, Ender Karaca, Amy Goldstein, Stefania Bigoni, L. I. Al Gazali, Laila Bastaki, Jean Messer, E. Del Giudice, M. Cazzagon, A. Permunian, C. Ae Kim, Edward Blair, M. Di Giacomo, E. DeMarco, Melissa Lees, Renato Borgatti, Marilena Briguglio, H. Raynes, Renaud Touraine, Andreas Zankl, E. Finsecke, Itxaso Marti, Lorenzo Pinelli, S. Romano, Isabelle Perrault, Jane A. Hurst, Eamonn Sheridan, Kenton R. Holden, T. E. Gallager, P. De Lonlay, M. L. Di Sabato, Marina Michelson, Hülya Kayserili, Terry D. Sanger, Heike Philippi, Patrizia Accorsi, M. Silengo, Miriam Iannicelli, Lorena Travaglini, K. Dias, Gianluca Caridi, Loredana Boccone, J. Johannsdottir, R. De Vescovi, P. Ludvigsson, J. Hahn, Tania Attié-Bitach, Franco Stanzial, Silvia Battaglia, Francesco Brancati, Ghada M. H. Abdel-Salam, William B Dobyns, Enrico Bertini, Daria Riva, F. Benedicenti, Joseph G. Gleeson, Ryan D. Schubert, Roshan Koul, Kalpathy S. Krishnamoorthy, Luigina Spaccini, G. Uziel, Jean-Michel Rozet, M.A. Donati, Marzia Pollazzon, Sophie Audollent, Matloob Azam, Alex Magee, A. Adami, Ignacio Pascual-Castroviejo, Bernard Stuart, Rita Fischetto, Darryl C. De Vivo, Christopher A. Walsh, Asma A. Al-Tawari, Carla Uggetti, Alessandra Ferlini, Atıl Yüksel, Enza Maria Valente, Agnese Suppiej, Faustina Lalatta, Lucio Giordano, Maria Roberta Cilio, Bernard L. Maria, Trudy McKanna, S. Sigaudy, L. Demerleir, Carmelo Salpietro, Henry Sanchez, Bruria Ben-Zeev, A. Pessagno, Elisa Fazzi, J. Milisa, Shubha R. Phadke, D. Greco, Dominika Swistun, Yves Sznajer, B. Rodriguez, Silvana Briuglia, V. Udani, Francesca Faravelli, Maha S. Zaki, S. Bernes, Maria Teresa Divizia, C. Daugherty, David G. Brooks, Clara Barbot, László Sztriha, C. Donahue, Wendy K. Chung, Dean Sarco, Pierangela Castorina, Petter Strømme, Pasquale Parisi, Andreas R. Janecke, Roberta Battini, L. Martorell Sampol, M. Akcakus, Angela Barnicoat, Jerlyn C Tolentino, Dorit Lev, A. Seward, Banu Anlar, Corrado Romano, D. Nicholl, A. Moreira, Alice Abdel-Aleem, Padraic Grattan-Smith, C. G. Woods, Gustavo Maegawa, Alessandro Simonati, Kathryn J. Swoboda, David Viskochil, Luciana Rigoli, R. Van Coster, André Mégarbané
Publikováno v:
American Journal of Medical Genetics, Part A, 149(10), 2173-2180. Wiley-Liss Inc.
American journal of medical genetics. Part A, 149A(10), 2173-2180. Wiley-Liss Inc.
International JSRD Study Group 2009, ' Expanding CEP290 mutational spectrumin ciliopathies ', American Journal of Medical Genetics, Part A, vol. 149, no. 10, pp. 2173-2180 . https://doi.org/10.1002/ajmg.a.33025
American journal of medical genetics. Part A, 149A(10), 2173-2180. Wiley-Liss Inc.
International JSRD Study Group 2009, ' Expanding CEP290 mutational spectrumin ciliopathies ', American Journal of Medical Genetics, Part A, vol. 149, no. 10, pp. 2173-2180 . https://doi.org/10.1002/ajmg.a.33025
Ciliopathies are an expanding group of rare conditions characterized by multiorgan involvement, that are caused by mutations in genes encoding for proteins of the primary cilium or its apparatus. Among these genes, CEP290 bears an intriguing allelic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f64afa39636eb3bd0d703cd79fea0af0
https://doi.org/10.1002/ajmg.a.33025
https://doi.org/10.1002/ajmg.a.33025
Autor:
W.T.A. van der Graaf, E.G.E. de Vries, Michael Schaapveld, Ilja M. Nolte, M M de Jong, Jan H. Kleibeuker, G. J. Te Meerman, Jan C. Oosterwijk
Publikováno v:
Journal of medical genetics. 39(4)
This review focuses on genes other than the high penetrance genes BRCA1 and BRCA2 that are involved in breast cancer susceptibility. The goal of this review is the discovery of polymorphisms that are either associated with breast cancer or that are i