Zobrazeno 1 - 10
of 39
pro vyhledávání: '"B. Gómez García"'
Autor:
Delal Akdeniz, Mark van Barele, Bernadette A.M. Heemskerk-Gerritsen, Ewout W. Steyerberg, Michael Hauptmann, Irma van de Beek, Klaartje van Engelen, Marijke R. Wevers, Encarnacion B. Gómez García, Margreet G.E.M. Ausems, Lieke P.V. Berger, Christi J. van Asperen, Muriel A. Adank, Margriet J. Collée, Denise J. Stommel-Jenner, Agnes Jager, Marjanka K. Schmidt, Maartje J. Hooning
Publikováno v:
Breast, Vol 61, Iss , Pp 98-107 (2022)
Aim: BRCA1/2 mutation carriers with primary breast cancer (PBC) are at high risk of contralateral breast cancer (CBC). In a nationwide cohort, we investigated the effects of chemotherapeutic agents given for PBC on CBC risk separately in BRCA1 and BR
Externí odkaz:
https://doaj.org/article/f07b5cdd82d14cf6b8c51743fa5578cb
Autor:
Mercedes Robledo, Anne-Paule Gimenez-Roqueplo, Graeme Eisenhofer, Giuseppe Opocher, Patricia L. M. Dahia, Massimo Mannelli, Karel Pacak, Felix Beuschlein, Miguel Urioste, Carli M.J. Tops, Henri J.L.M. Timmers, Elisa Taschin, Carlos Suarez, Alexander P.A. Stegmann, Frank Schillo, Macarena Ruiz-Ferrer, Giovanna Roncador, Nicole Reisch, Victoria Raymond, Elena Rapizzi, Nan Qin, Miguel Quesada-Charneco, Tamara Prodanov, Pierre-François Plouin, Peggy Pierre, Arnaud Murat, Luigi Mori, Anna Merlo, Arjen R. Mensenkamp, Rocío Letón, Jacques W.M. Lenders, Esther Korpershoek, Emiliano Honrado, Frederik J. Hes, Isabelle Guilhem, Álvaro Gómez-Graña, Encarna B. Gómez-García, Xavier Girerd, Tonino Ercolino, Ronald R. de Krijger, Mara Giacchè, Eleonora P.M. Corssmit, María-Dolores Chiara, Philippe Chanson, Maurizio Castellano, Salud Borrego, Sara Bobisse, Marinus J. Blok, Yves-Jean Bignon, Jérôme Bertherat, Sandra Bernaldo de Quirós, Marta Barontini, Laurence Amar, Aguirre A. de Cubas, Lucía Inglada-Pérez, Nasséra Abermil, Iñaki Comino-Méndez, Nicole Paes Morales, Francesca Schiavi, Alberto Cascón, Nelly Burnichon
Purpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest–derived neoplasms. Recently we identified germline mutations in a new tumor suppressor susceptibility gene, MAX (MYC-associated factor X), which pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e186187a379b455e8e5d962b4e1b154
https://doi.org/10.1158/1078-0432.c.6520958.v1
https://doi.org/10.1158/1078-0432.c.6520958.v1
Autor:
Anne M L Jansen, Marije A Geilenkirchen, Tom van Wezel, Shantie C Jagmohan-Changur, Dina Ruano, Heleen M van der Klift, Brendy E W M van den Akker, Jeroen F J Laros, Michiel van Galen, Anja Wagner, Tom G W Letteboer, Encarna B Gómez-García, Carli M J Tops, Hans F Vasen, Peter Devilee, Frederik J Hes, Hans Morreau, Juul T Wijnen
Publikováno v:
PLoS ONE, Vol 11, Iss 6, p e0157381 (2016)
BACKGROUND AND AIMS:Lynch Syndrome (LS) is caused by pathogenic germline variants in one of the mismatch repair (MMR) genes. However, up to 60% of MMR-deficient colorectal cancer cases are categorized as suspected Lynch Syndrome (sLS) because no path
Externí odkaz:
https://doaj.org/article/d3a653d49cec4ce4a0f3cab6d6023e4e
Autor:
Aben Essid, Lotfi Miladi, Jean Bergounioux, B. Mbieleu, Christophe Glorion, Mathilde Gaume, Viviane Azzi-Salameh, Ivana Dabaj, Audrey Benezit, Susana Quijano-Roy, Christine Barnerias, Isabelle Doehring, Isabelle Desguerre, Marta B. Gómez-García de la Banda, Etienne Saudeau, Delphine Verollet, Vicken Topouchian
Publikováno v:
Journal of Pediatric Orthopaedics.
Background Treatment of spinal muscular atrophy (SMA) scoliosis has evolved in the last decade, with the emergence of fusionless surgical techniques that allow correction of the deformity before the end of growth spurt. These techniques are expected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e923bdc2295d4c62dfd4f7c2b8c28d8
https://doi.org/10.1097/bpo.0000000000001897
https://doi.org/10.1097/bpo.0000000000001897
Autor:
Alessandro Amaddeo, Julien Durigneux, Christine Barnerias, Ivana Dabaj, Susana Quijano-Roy, Robert Carlier, Brigitte Fauroux, Isabelle Desguerre, Audrey Benezit, Sandrine Pruvost, Marta B. Gómez-García de la Banda, Sonia Khirani
Publikováno v:
Pediatric Pulmonology
Pediatric Pulmonology, Wiley, 2021, 56 (1), pp.299-306. ⟨10.1002/ppul.25142⟩
Pediatric Pulmonology, Wiley, 2021, 56 (1), pp.299-306. ⟨10.1002/ppul.25142⟩
International audience; Introduction: Nusinersen is associated with an improvement in motor function in children with spinal muscular atrophy (SMA) but data on respiratory muscles strength are scarce. Respiratory muscles performance and lung function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9daee0d4d3afe250cfbbb75e245f7e5e
https://hal.archives-ouvertes.fr/hal-03127510
https://hal.archives-ouvertes.fr/hal-03127510
Autor:
Tomas Kirchhoff, Mia M Gaudet, Antonis C Antoniou, Lesley McGuffog, Manjeet K Humphreys, Alison M Dunning, Stig E Bojesen, Børge G Nordestgaard, Henrik Flyger, Daehee Kang, Keun-Young Yoo, Dong-Young Noh, Sei-Hyun Ahn, Thilo Dork, Peter Schürmann, Johann H Karstens, Peter Hillemanns, Fergus J Couch, Janet Olson, Celine Vachon, Xianshu Wang, Angela Cox, Ian Brock, Graeme Elliott, Malcolm W R Reed, Barbara Burwinkel, Alfons Meindl, Hiltrud Brauch, Ute Hamann, Yon-Dschun Ko, GENICA Network, Annegien Broeks, Marjanka K Schmidt, Laura J Van 't Veer, Linde M Braaf, Nichola Johnson, Olivia Fletcher, Lorna Gibson, Julian Peto, Clare Turnbull, Sheila Seal, Anthony Renwick, Nazneen Rahman, Pei-Ei Wu, Jyh-Cherng Yu, Chia-Ni Hsiung, Chen-Yang Shen, Melissa C Southey, John L Hopper, Fleur Hammet, Thijs Van Dorpe, Anne-Sophie Dieudonne, Sigrid Hatse, Diether Lambrechts, Irene L Andrulis, Natalia Bogdanova, Natalia Antonenkova, Juri I Rogov, Daria Prokofieva, Marina Bermisheva, Elza Khusnutdinova, Christi J van Asperen, Robert A E M Tollenaar, Maartje J Hooning, Peter Devilee, Sara Margolin, Annika Lindblom, Roger L Milne, José Ignacio Arias, M Pilar Zamora, Javier Benítez, Gianluca Severi, Laura Baglietto, Graham G Giles, kConFab, AOCS Study Group, Amanda B Spurdle, Jonathan Beesley, Xiaoqing Chen, Helene Holland, Sue Healey, Shan Wang-Gohrke, Jenny Chang-Claude, Arto Mannermaa, Veli-Matti Kosma, Jaana Kauppinen, Vesa Kataja, Bjarni A Agnarsson, Maria A Caligo, Andrew K Godwin, Heli Nevanlinna, Tuomas Heikkinen, Zachary Fredericksen, Noralane Lindor, Katherine L Nathanson, Susan M Domchek, SWE-BRCA, Niklas Loman, Per Karlsson, Marie Stenmark Askmalm, Beatrice Melin, Anna von Wachenfeldt, HEBON, Frans B L Hogervorst, Martijn Verheus, Matti A Rookus, Caroline Seynaeve, Rogier A Oldenburg, Marjolijn J Ligtenberg, Margreet G E M Ausems, Cora M Aalfs, Hans J P Gille, Juul T Wijnen, Encarna B Gómez García, EMBRACE, Susan Peock, Margaret Cook, Clare T Oliver, Debra Frost, Craig Luccarini, Gabriella Pichert, Rosemarie Davidson, Carol Chu, Diana Eccles, Kai-Ren Ong, Jackie Cook, Fiona Douglas, Shirley Hodgson, D Gareth Evans, Rosalind Eeles, Bert Gold, Paul D P Pharoah, Kenneth Offit, Georgia Chenevix-Trench, Douglas F Easton, BCAC/CIMBA
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e35706 (2012)
Recently, a locus on chromosome 6q22.33 (rs2180341) was reported to be associated with increased breast cancer risk in the Ashkenazi Jewish (AJ) population, and this association was also observed in populations of non-AJ European ancestry. In the pre
Externí odkaz:
https://doaj.org/article/1433592c7c844e02a12dd57e5bf1a0a8
Autor:
E. B. Gómez García, M. B. I. Lobbes, K. van de Vijver, K. Keymeulen, F. van der Ent, H. G. Yntema, V. C. Tjan-Heijnen, C. Boetes
Publikováno v:
Case Reports in Radiology, Vol 2012 (2012)
Cowden syndrome (CS) is an autosomal dominant disorder characterized by presence of multiple hamartomas, and other benign and malignant abnormalities of the breasts, skin, thyroid, endometrium, gastrointestinal tract, and central nervous system. Hama
Externí odkaz:
https://doaj.org/article/4457536be757438691b47df22ae58343
Publikováno v:
Leerboek oncologie ISBN: 9789036804417
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e586645f19b1ed6966d348c9b86ae577
https://doi.org/10.1007/978-90-368-0442-4_2
https://doi.org/10.1007/978-90-368-0442-4_2
Autor:
M.J. Richart Rufino, J. Navas Cutanda, F. Rivera Casares, B. Gómez García, E. Rodríguez Górriz, C. Gómez Moruno
Publikováno v:
Atención Primaria. 36(1):14-18
ObjetivoVerificar si la información contenida en los soportes escritos que la industria farmacéutica entrega a los medicos de familia se deriva de los estudios científicos que la avalan.DiseñoEstudio transversal.EmplazamientoCentro de salud de la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0a46e4708eb4065d126e4ee55d3810f
Autor:
Encarna B. Gómez García, Diederik W.J. Dippel, Marie-Louise van Goor, Geert Jan Brouwers, Peter J. Koudstaal, Frank W.G. Leebeek
Publikováno v:
Thrombosis and Haemostasis. 93:92-96
SummaryHigh levels of plasminogen activator inhibitor type 1 (PAI-1) have been implicated as a risk factor for cardiovascular disease, but its precise role remains controversial.The 4G allele of the PAI-1 4G/5G promoter polymorphism is associated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f1e3a7fb24f67f9330cf20be1e60844
https://doi.org/10.1160/th04-09-0560
https://doi.org/10.1160/th04-09-0560