Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population‐based study von Rosso, Sonia M., Kaat, Laura Donker, Baks, Timo, Joosse, Marijke, de Koning, Inge, Pijnenburg, Yolande, de Jong, Daniëlle, Dooijes, Dennis, Kamphorst, Wouter, Ravid, Rivka, Niermeijer, Martinus F., Verheij, Frans, Kremer, H. P., Scheltens, Philip, van Duijn, Cornelia M., Heutink, Peter, van Swieten, John C.

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Breast Cancer after Prophylactic Bilateral Mastectomy in Women with a BRCA1 or BRCA2 Mutation von Meijers-Heijboer, Hanne, van Geel, Bert, van Putten, Wim L.J, Henzen-Logmans, Sonja C, Seynaeve, Caroline, Menke-Pluymers, Marian B.E, Bartels, Carina C.M, Verhoog, Leon C, van den Ouweland, Ans M.W, Niermeijer, Martinus F, Brekelmans, Cecile T.M, Klijn, Jan G.M

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High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands von Rizzu, Patrizia, Van Swieten, John C., Joosse, Marijke, Hasegawa, Masato, Stevens, Martijn, Tibben, Aad, Niermeijer, Martinus F., Hillebrand, Marcel, Ravid, Rivka, Oostra, Ben A., Goedert, Michel, van Duijn, Cornelia M., Heutink, Peter

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Clinical studies on submicroscopic subtelomeric rearrangements: a checklist von de Vries, B B A, White, S M, Knight, S J L, Regan, R, Homfray, T, Young, I D, Super, M, McKeown, C, Splitt, M, Quarrell, O W J, Trainer, A H, Niermeijer, M F, Malcolm, S, Flint, J, Hurst, J A, Winter, R M

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Frontotemporal Dementia: Behavioral Symptoms and Caregiver Distress von Mourik, J.C., Rosso, S.M., Niermeijer, M.F., Duivenvoorden, H.J., van Swieten, J.C., Tibben, A.

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Genotype versus phenotype in families with androgen insensitivity syndrome von BOEHMER, Annemie L. M, BRÜGGENWIRTH, Hennie, KLEIJER, Wim J, VAN DER KWAST, Theo H, DE VROEDE, Monique A, DROP, Stenvert L. S, VAN ASSENDELFT, Cissy, OTTEN, Barto J, VERLEUN-MOOIJMAN, Marja C. T, NIERMEIJER, Martinus F, BRUNNER, Han G, ROUWE, Catrienus W, WAELKENS, J. J, OOSTDIJK, Wilma

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Phenotypic variation in hereditary frontotemporal dementia with tau mutations von Van Swieten, J. C., Stevens, M., Rosso, S. M., Rizzu, P., Joosse, M., De Koning, I., Kamphorst, W., Ravid, R., Spillantini, M. G., Niermeijer, M. F., Heutink, P.

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Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy von Seynaeve, C, Verhoog, L.C, van de Bosch, L.M.C, van Geel, A.N, Menke-Pluymers, M, Meijers-Heijboer, E.J, van den Ouweland, A.M.W, Wagner, A, Creutzberg, C.L, Niermeijer, M.F, Klijn, J.G.M, Brekelmans, C.T.M

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LMNA , encoding lamin A/C, is mutated in partial lipodystrophy von Trembath, Richard C, Shackleton, Sue, Lloyd, David J, Jackson, Stephen N.J, Evans, Richard, Niermeijer, Martinus F, Singh, Baldev M, Schmidt, Hartmut, Brabant, Georg, Kumar, Sudesh, Durrington, Paul N, Gregory, Simon, O'Rahilly, Stephen

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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree von Wagner, A, Hendriks, Y, Meijers-Heijboer, E J, de Leeuw, W J F, Morreau, H, Hofstra, R, Tops, C, Bik, E, Bröcker-Vriends, A H J T, van der Meer, C, Lindhout, D, Vasen, H F A, Breuning, M H, Cornelisse, C J, van Krimpen, C, Niermeijer, M F, Zwinderman, A H, Wijnen, J, Fodde, R

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One year follow-up of women opting for presymptomatic testing for BRCA1 and BRCA2: emotional impact of the test outcome and decisions on risk management (surveillance or prophylact... von LODDER, Litanja N, FRETS, Petra G, BREKELMANS, Cecile T. M, BURGER, Curt W, NIERMEIJER, Martinus F, TRIJSBURG, R. Willem, MEIJERS-HEIJBOER, E. Johanna, KLIJN, Jan G. M, SEYNAEVE, Caroline, VAN GEEL, Albertus N, TILANUS, Madeleine M. A, BARTELS, Carina C. M, VERHOOG, Leon C

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Familial aggregation in frontotemporal dementia von STEVENS, M, VAN DUIJN, C. M, VAN SWIETEN, J. C, KAMPHORST, W, DE KNIJFF, P, HEUTINK, P, VAN GOOL, W. A, SCHELTENS, P, RAVID, R, OOSTRA, B. A, NIERMEIJER, M. F

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A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease von Rosso, Sonia M., Van Herpen, Esther, Deelen, Wout, Kamphorst, Wouter, Severijnen, Lies-Anne, Willemsen, Rob, Ravid, Rivka, Niermeijer, Martinus F., Dooijes, Dennis, Smith, Michael J., Goedert, Michel, Heutink, Peter, Van Swieten, John C.

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Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three dutch families von Heutink, P., Stevens, M., Rizzu, P., Bakker, E., Kros, J. M., Tibben, A., Niermeijer, M. F., Van Duijn, C. M., Oostra, B. A., Van Swieten, J. C.

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Three new families with arterial tortuosity syndrome von Wessels, Marja W., Catsman-Berrevoets, Coriene E., Mancini, Grazia M.S., Breuning, Martijn H., Hoogeboom, Jeanette J.M., Stroink, Hans, Frohn-Mulder, Ingrid, Coucke, Paul J., Paepe, Anne De, Niermeijer, Martinus F., Willems, Patrick J.

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Psychological studies in Huntington's disease: making up the balance von Duisterhof, Magdalena, Trijsburg, Rutger W, Niermeijer, Martinus F, Roos, Raymund A C, Tibben, Aad

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Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey von de Vries, Bert B.A., van den Ouweland, Ans M.W., Mohkamsing, Serieta, Duivenvoorden, Hugo J., Mol, Esther, Gelsema, Kirsten, Rijn, Monique van, Halley, Dicky J.J., Sandkuijl, Lodewijk A., Oostra, Ben A., Tibben, Aad, Niermeijer, Martinus F.

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Autosomal dominant inheritance of left ventricular outflow tract obstruction von Wessels, Marja W., Berger, Rolf M.F., Frohn-Mulder, Ingrid M.E., Roos-Hesselink, Jolien W., Hoogeboom, Jeanette J.M., Mancini, Grazia S., Bartelings, Margot M., Krijger, Ronald de, Wladimiroff, Jury W., Niermeijer, Martinus F., Grossfeld, Paul, Willems, Patrick J.

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What do women really want to know? Motives for attending familial breast cancer clinics von van Asperen, C J, van Dijk, S, Zoeteweij, M W, Timmermans, D R M, de Bock, G H, Meijers-Heijboer, E J, Niermeijer, M F, Breuning, M H, Kievit, J, Otten, W

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The fragile X syndrome von de Vries, B B, Halley, D J, Oostra, B A, Niermeijer, M F

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