Diagnostic tests for the detection of peripheral neuropathy von VERHOEVEN KRISTIEN, BROECKHOVEN CHRISTINE V, JONGHE PETER D, TIMMERMAN VINCENT

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Diagnostic tests for the detection of motor neuropathy von DE JONGHE PETER, BROECKHOVEN CHRISTINE V, TIMMERMAN VINCENT, IROBI JOY

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APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy von Sleegers, Kristel, Brouwers, Nathalie, Gijselinck, Ilse, Theuns, Jessie, Goossens, Dirk, Wauters, Jan, Del-Favero, Jurgen, Cruts, Marc, Duijn, Cornelia M. van, Broeckhoven, Christine Van

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Promoter Mutations That Increase Amyloid Precursor-Protein Expression Are Associated with Alzheimer Disease von Theuns, Jessie, Brouwers, Nathalie, Engelborghs, Sebastiaan, Sleegers, Kristel, Bogaerts, Veerle, Corsmit, Ellen, De Pooter, Tim, van Duijn, Cornelia M., De Deyn, Peter P., Van Broeckhoven, Christine

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Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease von Brouwers, Nathalie, Sleegers, Kristel, Engelborghs, Sebastiaan, Bogaerts, Veerle, Serneels, Sally, Kamali, Kenan, Corsmit, Ellen, Leenheir, Evelyn De, Martin, Jean-Jacques, De Deyn, Peter P., Broeckhoven, Christine Van, Theuns, Jessie

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis von Aulchenko, Yurii S, Hoppenbrouwers, Ilse A, Ramagopalan, Sreeram V, Broer, Linda, Jafari, Naghmeh, Hillert, Jan, Link, Jenny, Lundström, Wangko, Greiner, Eva, Dessa Sadovnick, A, Goossens, Dirk, Van Broeckhoven, Christine, Del-Favero, Jurgen, Ebers, George C, Oostra, Ben A, van Duijn, Cornelia M, Hintzen, Rogier Q

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Highly efficient gene delivery by mRNA electroporation in human hematopoietic cells: superiority to lipofection and passive pulsing of mRNA and to electroporation of plasmid cDNA f... von Van Tendeloo, Viggo F.I., Ponsaerts, Peter, Lardon, Filip, Nijs, Griet, Lenjou, Marc, Van Broeckhoven, Christine, Van Bockstaele, Dirk R., Berneman, Zwi N.

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Clinical Phenotypes of Different MPZ (P 0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination von Warner, Laura E, Hilz, Max J, Appel, Stanley H, Killian, James M, Kolodny, Edwin H, Karpati, George, Carpenter, Stirling, Watters, Gordon V, Wheeler, Calvin, Witt, David, Bodell, Adria, Nelis, Eva, Van Broeckhoven, Christine, Lupski, James R

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PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease von Dermaut, Bart, Croes, Esther A., Rademakers, Rosa, Van Den Broeck, Marleen, Cruts, Marc, Hofman, Albert, Van Duijn, Cornelia M., Van Broeckhoven, Christine

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Genetic Association of Apolipoprotein E with Age-Related Macular Degeneration von Klaver, Caroline C.W., Kliffen, Mike, van Duijn, Cornelia M., Hofman, Albert, Cruts, Marc, Grobbee, Diederick E., van Broeckhoven, Christine, de Jong, Paulus T.V.M.

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Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E von De Jonghe, Peter, Mersivanova, Irina, Nelis, Eva, Del Favero, Jurgen, Martin, Jean-Jacques, Van Broeckhoven, Christine, Evgrafov, Oleg, Timmerman, Vincent

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Molecular biological characterization of an azole-resistant Candida glabrata isolate von MARICHAL, P, VANDEN BOSSCHE, H, ODDS, F. C, NOBELS, G, WARNOCK, D. W, TIMMERMAN, V, VAN BROECKHOVEN, C, FAY, S, MOSE-LARSEN, P

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Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression von THEUNS, J, DEL-FAVERO, J, DERMAUT, B, VAN DUIJN, C. M, BACKHOVENS, H, VAN DEN BROECK, M, SERNEELS, S, CORSMIT, E, VAN BROECKHOVEN, C, CRUTS, M

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Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study von Nelis, E, Van Broeckhoven, C, De Jonghe, P, Löfgren, A, Vandenberghe, A, Latour, P, Le Guern, E, Brice, A, Mostacciuolo, M L, Schiavon, F, Palau, F, Bort, S, Upadhyaya, M, Rocchi, M, Archidiacono, N, Mandich, P, Bellone, E, Silander, K, Savontaus, M L, Navon, R, Goldberg-Stern, H, Estivill, X, Volpini, V, Friedl, W, Gal, A

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Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients von Mersiyanova, Irina V., Ismailov, Sookhrat M., Polyakov, Alexandr V., Dadali, Elena L., Fedotov, Valeriy P., Nelis, Eva, Löfgren, Ann, Timmerman, Vincent, Van Broeckhoven, Christine, Evgrafov, Oleg V.

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Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies von BORT, S, NELIS, E, VAN BROECKHOVEN, C, PALAU, F, TIMMERMAN, V, SEVILLA, T, CRUZ-MARTINEZ, A, MARTINEZ, F, MILLAN, J. M, ARPA, J, VILCHEZ, J. J, PRIETO, F

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Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene von Hendriks, Lydia, van Duijn, Cornelia M., Cras, Patrick, Cruts, Marc, Van Hul, Wim, van Harskamp, Frans, Warren, Andrew, McInnis, Melvin G., Antonarakis, Stylianos E., Martin, Jean-Jacques, Hofman, Albert, Van Broeckhoven, Christine

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A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21 von Ismailov, S M, Fedotov, V P, Dadali, E L, Polyakov, A V, Van Broeckhoven, C, Ivanov, V I, De Jonghe, P, Timmerman, V, Evgrafov, O V

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Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3 von Van Broeckhoven, Christine, Backhovens, Hubert, Cruts, Marc, De Winter, Goedele, Bruyland, Marc, Cras, Patrick, Martin, Jean-Jacques

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Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease von Cruts, Marc, Dermaut, Bart, Rademakers, Rosa, Roks, Gerwin, Van den Broeck, Marleen, Munteanu, Gabriela, van Duijn, Cornelia M, Van Broeckhoven, Christine

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