Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Christiana Willems"'
Autor:
Ellen Gelpi, Mathieu Vandenbulcke, Yalda Baradaran-Heravi, Alex Michotte, Alexandre de Mendonça, Elisa Bonomi, Peter Paul De Deyn, Peter Heutink, Bruno Bergmans, Matthew J. Fraidakis, Matthis Synofzik, Dirk Peeters, Eva Parobkova, Christine Van Broeckhoven, Patrick Santens, Peter De Jonghe, Radoslav Matej, Maria Rosário Almeida, Rik Vandenberghe, Hung Phuoc Nguyen, Pau Pastor, Alessandro Padovani, Gabriel Miltenberger-Miltenyi, Jan De Bleecker, Philip Van Damme, Sara Van Mossevelde, Isabel Santana, Ricard Rojas-García, Olivier Deryck, Julie van der Zee, Eric Salmon, Ana Verdelho, Christiana Willems, Nina De Klippel, Miquel Aguilar, Lubina Dillen, Alberto Lleó, Sergi Borrego-Écija, Sebastiaan Engelborghs, Sandro Sorbi, Jonathan Baets, Camilla Ferrari, Monica Diez-Fairen, Silvia Bagnoli, Barbara Borroni, Raquel Sánchez-Valle, Johan Goeman, Anne Sieben, Ignacio Illán-Gala, Patrick Cras, Panagiotis Alexopoulos, Janina Turon-Sans, Benedetta Nacmias, Adrian Ivanoiu, Irene Piaceri, Janine Diehl-Schmid, Jan Versijpt, Silvana Archettim, C. Ferreira, Frederico Simões do Couto, Jordi Clarimón, Dirk Nuytten, Javier Simón-Sánchez, Carlo Wilke
Publikováno v:
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging, Vol. 69, p. 293.e9-293.e11 (2018)
Neurobiology of aging
Neurobiology of aging 69, 293.e9-293.e11 (2018). doi:10.1016/j.neurobiolaging.2018.05.005
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging, Vol. 69, p. 293.e9-293.e11 (2018)
Neurobiology of aging
Neurobiology of aging 69, 293.e9-293.e11 (2018). doi:10.1016/j.neurobiolaging.2018.05.005
We evaluated the genetic contribution of the T cell-restricted intracellular antigen-1 gene (TIA1) in a European cohort of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) patients. Exonic resequencing of TIA1 in 1120 patients (6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32b1513e7629a84ce2ff2b34a8260b64
https://lirias.kuleuven.be/handle/123456789/661661
https://lirias.kuleuven.be/handle/123456789/661661
Autor:
Albert Lladó, Jordi Clarimón, Barbara Borroni, Roberta Ghidoni, Rik Vandenberghe, Giovanni B. Frisoni, Isabel Santana, Alberto Lleó, Sara Van Mossevelde, Christiana Willems, Benedetta Nacmias, Mathieu Vandenbulcke, Mercè Boada, Adrian Ivanoiu, Giuliano Binetti, Maria Rosário Almeida, Peter Paul De Deyn, Marc Cruts, Monica Diez-Fairen, Miquel Aguilar, Anne Sieben, Marleen Van den Broeck, Gabriel Miltenberger-Miltenyi, Eline Wauters, Christine Van Broeckhoven, Patrick Cras, Raquel Sánchez-Valle, Estrella Gómez-Tortosa, Sandro Sorbi, Isabel Hernández, Ellen Gelpi, Agustín Ruiz, Julie van der Zee, Lubina Dillen, Alexandre de Mendonça, Luisa Benussi, Karin Peeters, Sebastiaan Engelborghs, Alessandro Padovani, Pau Pastor, Stéphanie Philtjens
Publikováno v:
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of Aging, Vol. 66 (2018) pp. 181.e3-181.e10
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Neurobiology of aging
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of Aging, Vol. 66 (2018) pp. 181.e3-181.e10
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Neurobiology of aging
© 2018 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
We investigated the genetic role of sortilin (SORT1) in frontotemporal dementia (FTD
We investigated the genetic role of sortilin (SORT1) in frontotemporal dementia (FTD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae5d3acf43be2e53ceda38dda5b8884
https://hdl.handle.net/11379/576260
https://hdl.handle.net/11379/576260
Autor:
Juan Fortea, Marc Cruts, Tobi Van den Bossche, Jan Versijpt, Alessandro Padovani, Luisa Benussi, Roberta Ghidoni, Alexandre de Mendonça, Elena Lorenzo, Manuel Seijo-Martínez, Jaume Campdelacreu, Sandro Sorbi, Radoslav Matej, Peter Paul De Deyn, Panagiotis Alexopoulos, Olivier Deryck, Albert Lladó, Pau Pastor, Frederico Simões do Couto, Rik Vandenberghe, Estrella Gómez-Tortosa, Zdenek Rohan, Jordi Clarimón, Anne Sieben, Jordi Gascon, Isabel Santana, Maria A. Pastor, Maria Koutroumani, Madalena Martins, Sebastiaan Engelborghs, Janine Diehl-Schmid, Christine Van Broeckhoven, Benedetta Nacmias, Patrick Santens, Lubina Dillen, Ilse Gijselinck, Giuliano Binetti, Silvia Bagnoli, Bruno Bergmans, Agustín Ruiz, Raquel Sánchez-Valle, Barbara Borroni, Maria Rosário Almeida, Kristel Sleegers, Ellen Gelpi, Adrian Ivanoiu, Bavo Heeman, Cristina Razquin, Magda Tsolaki, Elena Iglesias, Caroline Graff, Johan Goeman, Alberto Lleó, Valentina Bessi, Laura Fratiglioni, Jan Verheijen, Alex Michotte, Jan De Bleecker, Rafael Blesa, Julie van der Zee, Eric Salmon, Ramón Reñé, Dirk Nuytten, Mathieu Vandenbulcke, Bart Dermaut, Håkan Thonberg, Christiana Willems
Publikováno v:
Neurobiology of Aging
Neurobiology of aging, Vol. 62, p. 245.e1-245.e7 (2018)
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging
Neurobiology of aging, Vol. 62, p. 245.e1-245.e7 (2018)
NEUROBIOLOGY OF AGING
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurobiology of aging
TANK-binding kinase 1 (TBK1) loss-of-function (LoF) mutations are known to cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), often combined with memory deficits early in the disease course. We performed targeted resequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ed5857598d419a89a3fe6fb32883e4
http://hdl.handle.net/2158/1107096
http://hdl.handle.net/2158/1107096
Autor:
Eline Wauters, Sara Van Mossevelde, Kristel Sleegers, Julie van der Zee, Sebastiaan Engelborghs, Anne Sieben, Rik Vandenberghe, Stéphanie Philtjens, Marleen Van den Broeck, Karin Peeters, Ivy Cuijt, Wouter De Coster, Tim Van Langenhove, Patrick Santens, Adrian Ivanoiu, Patrick Cras, Jan L. De Bleecker, Jan Versijpt, Roeland Crols, Nina De Klippel, Jean-Jacques Martin, Peter P. De Deyn, Marc Cruts, Christine Van Broeckhoven, Johan Goeman, Dirk Nuytten, Mathieu Vandenbulcke, Alex Michotte, Eric Salmon, Olivier Deryck, Bruno Bergmans, Christiana Willems, Jean Delbeck
Publikováno v:
NEUROBIOLOGY OF AGING
Neurobiology of aging
Neurobiology of aging
We previously reported a granulin (GRN) null mutation, originating from a common founder, in multiple Belgian families with frontotemporal dementia. Here, we used data of a 10-year follow-up study to describe in detail the clinical heterogeneity obse
Autor:
Mathieu Vandenbulcke, Anne Sieben, Jonathan Baets, Rik Vandenberghe, Jan Versijpt, Christiana Willems, Olivier Deryck, Dirk Nuytten, Alex Michotte, Matthieu Moisse, Katrien Smets, Philip Van Damme, Jan De Bleecker, Jean Delbeck, Federica Perrone, Adrian Ivanoiu, Julie van der Zee, Eric Salmon, Sara Van Mossevelde, Jean-Jacques Martin, Christine Van Broeckhoven, Patrick Santens, Peter Paul De Deyn, Sebastiaan Engelborghs, Peter De Jonghe, Patrick Cras, Hung Phuoc Nguyen, Bruno Bergmans, Marc Bruyland
Publikováno v:
Neurobiology of aging
Mutation screening and phenotypic profiling of 2 amyotrophic lateral sclerosis-(ALS) and frontotemporal dementia-(FTD) associated genes, CHCHD10 and TUBA4A, were performed in a Belgian cohort of 459 FTD, 28 FTD-ALS, and 429 ALS patients. In CHCHD10,
Autor:
Isabel Santana, Estrella Gómez-Tortosa, Federica Perrone, Patrick Cras, Alexandre de Mendonça, Jonathan Baets, Panagiotis Alexopoulos, Peter De Jonghe, Alessandro Padovani, Giovanni B. Frisoni, Frederico Simões do Couto, Håkan Thonberg, Philip Van Damme, Silvia Testi, Peter Paul De Deyn, Roberta Ghidoni, Matthew J. Fraidakis, Marc Bruyland, Maria Rosário Almeida, Alex Michotte, Jordi Clarimón, Agustín Ruiz, Jean Delbeck, Ilse Gijselinck, Jennifer Just, Olivier Deryck, Raquel Sánchez-Valle, Wim Robberecht, Matthis Synofzik, Giuliano Binetti, Adrian Ivanoiu, Sara Ortega-Cubero, Rik Vandenberghe, Isabel Hernández, Walter Maetzler, Ludger Schöls, Robert Perneczky, Kristel Sleegers, Ellen Gelpi, Alberto Lleó, Christine Van Broeckhoven, Julie van der Zee, Mercè Boada, Lubina Dillen, Eric Salmon, Marc Cruts, Patrick Santens, Sebastiaan Engelborghs, Janine Diehl-Schmid, Albert Lladó, Gian Maria Fabrizi, Radoslav Matej, Silvia Bagnoli, Pau Pastor, Frank Jessen, Barbara Borroni, Dirk Nuytten, Adrian Danek, Jan Versijpt, Bavo Heeman, Stayko Sarafov, Caroline Graff, Benedetta Nacmias, Luisa Benussi, Bart Dermaut, Johan Goeman, Michael T. Heneka, Katrien Smets, Gabor G. Kovacs, Christiana Willems, Sara Van Mossevelde, Albena Jordanova, Jan De Bleecker, Ricardo Rojas-García, Alfredo Ramirez, Bruno Bergmans, Ivailo Tournev, Veerle Bäumer, Gabriel Miltenberger-Miltenyi, Sandro Sorbi
Publikováno v:
Human Mutation, Vol. 38, No 3 (2017) pp. 297-309
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Human Mutation
Human mutation
Human mutation 38(3), 297-309 (2017). doi:10.1002/humu.23161
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
HUMAN MUTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Instituto de Salud Carlos III (ISCIII)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Human Mutation
Human mutation
Human mutation 38(3), 297-309 (2017). doi:10.1002/humu.23161
© 2016 The Authors. **Human Mutation published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::109e18977c1b5c191638868beaace792
http://hdl.handle.net/10044/1/45933
http://hdl.handle.net/10044/1/45933
Autor:
Marie-Claire D'Hooghe, Véronique Bissay, Eric De Smet, Erwin Van Ingelghem, Olivier Bouquiaux, Etienne Urbain, Katelijne Peeters, Daniel Guillaume, Andreas Lysandropoulos, Johan Caekebeke, Jana Debruyne, Pierrette Seeldrayers, Annick Melin, Pierre Denayer, Vincent Van Pesch, Ludo Vanopdenbosch, D Decoo, Inge Declercq, Patrick Vanderdonckt, Robert Medaer, Rémy Phan Ba, Bart Van Wijmeersch, Christian Sindic, Christiana Willems, Souraya El Sankari, Michel Dupuis, Anoek Symons, Barbara Willekens, Alain Maertens De Noordhout, Cécile Retif, Bénédicte Dubois, William van Landegem, Michel Bureau, Karine Geens, Emmanuel Bartholomé, Erwin Vanroose
Publikováno v:
Acta neurologica Belgica
Natalizumab (Tysabri(A (R))) is highly efficacious in controlling disease activity in relapsing multiple sclerosis (MS) patients. As it is one of the more recent therapies for MS, there remains a need for long-term safety and efficacy data of nataliz
Autor:
Veerle Bäumer, Alex Michotte, Jan De Bleecker, Patrick Cras, Githa Maes, Tim Van Langenhove, Anne Sieben, Mathieu Vandenbulcke, Christine Van Broeckhoven, Patrick Santens, Julie van der Zee, Peter De Jonghe, Olivier Deryck, Marleen Van den Broeck, Karin Peeters, Rik Vandenberghe, Maria Mattheijssens, Jan Versijpt, Ilse Gijselinck, Adrian Ivanoiu, Marc Cruts, Jean-Jacques Martin, Lubina Dillen, Sebastiaan Engelborghs, Peter Paul De Deyn, Christiana Willems, Stéphanie Philtjens
Publikováno v:
Jama neurology, 70(3), 365-373. AMER MEDICAL ASSOC
JAMA neurology
Vrije Universiteit Brussel
JAMA neurology
Vrije Universiteit Brussel
Objective: To characterize patients with frontotemporal lobar degeneration (FTLD) with a repeat expansion mutation in the gene C9orf72, and to determine whether there are differences in the clinical presentation compared with FTLD carriers of a mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c49b1401db83b0e60db76d381cbe7c7b
https://research.rug.nl/en/publications/d0a36128-e8ba-4600-b356-d7b1f74a77e8
https://research.rug.nl/en/publications/d0a36128-e8ba-4600-b356-d7b1f74a77e8
Publikováno v:
European journal of biochemistry. 8(1)
Under appropriate conditions, thyrotropin stimulated the binding of [131I]iodide to proteins in sheep, calf and dog thyroid slices. In dog thyroid slices, thyrotropin, dibutyl cyclic 3′:5′-adenosine monophosphate, and cyclic 3′:5′-AMP in the