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Gijselinck, Ilse, Van Mossevelde, Sara, van der Zee, Julie, Sieben, Anne, Philtjens, Stephanie, Heeman, Bavo, Engelborghs, Sebastiaan, Vandenbulcke, Mathieu, De Baets, Greet, Baumer, Veerle, Cuijt, Ivy, Van den Broeck, Marleen, Peeters, Karin, Mattheijssens, Maria, Rousseau, Frederic, Vandenberghe, Rik, De Jonghe, Peter, Cras, Patrick, De Deyn, Peter P., Martin, Jean-Jacques, Cruts, Marc, Van Broeckhoven, Christine
Veröffentlicht in: Gijselinck , I , Van Mossevelde , S , van der Zee , J , Sieben , A , Philtjens , S , Heeman , B , Engelborghs , S , Vandenbulcke , M , De Baets , G , Baumer , V , Cuijt , I , Van den Broeck , M , Peeters , K , Mattheijssens , M , Rousseau , F , Vandenberghe , R , De Jonghe , P , Cras , P , De Deyn , P P , Martin , J-J , Cruts , M , Van Broeckhoven , C & BELNEU Consortium 2015 , ' Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort ' , Neurology , vol. 85 , no. 24 , pp. 2116-2125 . https://doi.org/10.1212/WNL.0000000000002220;
2015
Veröffentlicht in: Gijselinck , I , Van Mossevelde , S , van der Zee , J , Sieben , A , Philtjens , S , Heeman , B , Engelborghs , S , Vandenbulcke , M , De Baets , G , Baumer , V , Cuijt , I , Van den Broeck , M , Peeters , K , Mattheijssens , M , Rousseau , F , Vandenberghe , R , De Jonghe , P , Cras , P , De Deyn , P P , Martin , J-J , Cruts , M , Van Broeckhoven , C & BELNEU Consortium 2015 , ' Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort ' , Neurology , vol. 85 , no. 24 , pp. 2116-2125 . https://doi.org/10.1212/WNL.0000000000002220;
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Koning, H., Postma, D.S., Brunekreef, B., Duiverman, E.J., Smit, H.A., Thijs, C., Penders, J., Kerkhof, M., Koppelman, G.H.
Veröffentlicht in: Koning , H , Postma , D S , Brunekreef , B , Duiverman , E J , Smit , H A , Thijs , C , Penders , J , Kerkhof , M & Koppelman , G H 2012 , ' Protocadherin-1 polymorphisms are associated with eczema in two Dutch birth cohorts ' , Pediatric Allergy and Immunology , vol. 23 , no. 3 , pp. 270-277 . https://doi.org/10.1111/j.1399-3038.2011.01201.x;
2012
Veröffentlicht in: Koning , H , Postma , D S , Brunekreef , B , Duiverman , E J , Smit , H A , Thijs , C , Penders , J , Kerkhof , M & Koppelman , G H 2012 , ' Protocadherin-1 polymorphisms are associated with eczema in two Dutch birth cohorts ' , Pediatric Allergy and Immunology , vol. 23 , no. 3 , pp. 270-277 . https://doi.org/10.1111/j.1399-3038.2011.01201.x;
2012
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Reumers, S.F.I., Erasmus, C.E., Bouman, K., Pennings, M., Schouten, M., Kusters, B., Duijkers, F.A.M., van der Kooi, A., Jaeger, B., Verschuuren-Bemelmans, C.C., Faber, C.G., van Engelen, B.G., Kamsteeg, E.J., Jungbluth, H., Voermans, N.C.
Veröffentlicht in: Reumers , S F I , Erasmus , C E , Bouman , K , Pennings , M , Schouten , M , Kusters , B , Duijkers , F A M , van der Kooi , A , Jaeger , B , Verschuuren-Bemelmans , C C , Faber , C G , van Engelen , B G , Kamsteeg , E J , Jungbluth , H & Voermans , N C 2021 , ' Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands ' , Clinical Genetics , vol. 100 , no. 6 , pp. 692-702 . https://doi.org/10.1111/cge.14054;
2021
Veröffentlicht in: Reumers , S F I , Erasmus , C E , Bouman , K , Pennings , M , Schouten , M , Kusters , B , Duijkers , F A M , van der Kooi , A , Jaeger , B , Verschuuren-Bemelmans , C C , Faber , C G , van Engelen , B G , Kamsteeg , E J , Jungbluth , H & Voermans , N C 2021 , ' Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands ' , Clinical Genetics , vol. 100 , no. 6 , pp. 692-702 . https://doi.org/10.1111/cge.14054;
2021
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Forsberg, Simon K. G., Kierczak, Marcin, Ljungvall, Ingrid, Merveille, Anne-Christine, Gouni, Vassiliki, Wiberg, Maria, Willesen, Jakob Lundgren, Hanas, Sofia, Lequarre, Anne-Sophie, Sorensen, Louise Mejer, Tiret, Laurent, McEntee, Kathleen, Seppälä, Eija, Koch, Jorgen, Battaille, Geraldine, Lohi, Hannes, Fredholm, Merete, Chetboul, Valerie, Haggstrom, Jens, Carlborg, Orjan, Lindblad-Toh, Kerstin, Hoglund, Katja
2015
2015
100
ten Dam, Leroy, Frankhuizen, Wendy S., Linssen, Wim H. J. P., Straathof, Chiara S., Niks, Erik H., Faber, Karin, Fock, Annemarie, Kuks, Jan B., Brusse, Esther, de Coo, Rene, Voermans, Nicol, Verrips, Aad, Hoogendijk, Jessica E., van Der Pol, Ludo, Westra, Dineke, de Visser, Marianne, van der Kooi, Anneke J., Ginjaar, Ieke
Veröffentlicht in: ten Dam , L , Frankhuizen , W S , Linssen , W H J P , Straathof , C S , Niks , E H , Faber , K , Fock , A , Kuks , J B , Brusse , E , de Coo , R , Voermans , N , Verrips , A , Hoogendijk , J E , van Der Pol , L , Westra , D , de Visser , M , van der Kooi , A J & Ginjaar , I 2019 , ' Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands : The clinical and molecular spectrum of 244 patients ' , Clinical Genetics , vol. 96 , no. 2 , pp. 126-133 . https://doi.org/10.1111/cge.13544;
2019
Veröffentlicht in: ten Dam , L , Frankhuizen , W S , Linssen , W H J P , Straathof , C S , Niks , E H , Faber , K , Fock , A , Kuks , J B , Brusse , E , de Coo , R , Voermans , N , Verrips , A , Hoogendijk , J E , van Der Pol , L , Westra , D , de Visser , M , van der Kooi , A J & Ginjaar , I 2019 , ' Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands : The clinical and molecular spectrum of 244 patients ' , Clinical Genetics , vol. 96 , no. 2 , pp. 126-133 . https://doi.org/10.1111/cge.13544;
2019