Desmin-related myopathy
van Spaendonck-Zwarts, KY, van Hessem, L, Jongbloed, JDH, de Walle, HEK, Capetanaki, Y, van der Kooi, AJ, van Langen, IM, van den Berg, MP, van Tintelen, JP
Published in Clinical genetics (01.10.2011)
Published in Clinical genetics (01.10.2011)
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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
Smit, DL, Mensenkamp, AR, Badeloe, S, Breuning, MH, Simon, MEH, Van Spaendonck, KY, Aalfs, CM, Post, JG, Shanley, S, Krapels, IPC, Hoefsloot, LH, Van Moorselaar, RJA, Starink, TM, Bayley, J-P, Frank, J, Van Steensel, MAM, Menko, FH
Published in Clinical genetics (01.01.2011)
Published in Clinical genetics (01.01.2011)
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Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers
van Gaalen, J., Maas, R. P. P. W. M., Ippel, E. F., Elting, M. W., van Spaendonck-Zwarts, K. Y., Vermeer, S., Verschuuren-Bemelmans, C., Timmann, D., van de Warrenburg, Bart P.
Published in Experimental brain research (01.02.2019)
Published in Experimental brain research (01.02.2019)
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Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families
Houweling, A C, Gijezen, L M, Jonker, M A, van Doorn, M B A, Oldenburg, R A, van Spaendonck-Zwarts, K Y, Leter, E M, van Os, T A, van Grieken, N C T, Jaspars, E H, de Jong, M M, Bongers, E M H F, Johannesma, P C, Postmus, P E, van Moorselaar, R J A, van Waesberghe, J-Htm, Starink, T M, van Steensel, M A M, Gille, J J P, Menko, F H
Published in British journal of cancer (06.12.2011)
Published in British journal of cancer (06.12.2011)
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Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?
Badeloe, S., Van Spaendonck-Zwarts, K.Y., Van Steensel, M.A.M., Van Marion, A.M.W., Van Essen, A.J., Jonkman, M.F., Steijlen, P.M., Poblete-Gutiérrez, P., Van Geel, M., Frank, J.
Published in British journal of dermatology (1951) (01.03.2009)
Published in British journal of dermatology (1951) (01.03.2009)
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Cognitive evaluation in adult patients with Möbius syndrome
VERZIJL, H. T. F. M, VAN ES, N, BERGER, H. J. C, PADBERG, G. W, VAN SPAENDONCK, K. P. M
Published in Journal of neurology (01.02.2005)
Published in Journal of neurology (01.02.2005)
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Circulating matrix γ‐carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome
CRANENBURG, E. C. M., VAN SPAENDONCK‐ZWARTS, K. Y., BONAFE, L., MITTAZ CRETTOL, L., RÖDIGER, L. A., DIKKERS, F. G., VAN ESSEN, A. J., SUPERTI‐FURGA, A., ALEXANDRAKIS, E., VERMEER, C., SCHURGERS, L. J., LAVERMAN, G. D.
Published in Journal of thrombosis and haemostasis (01.06.2011)
Published in Journal of thrombosis and haemostasis (01.06.2011)
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A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects
van der Linde, I. H. M., Hiemstra, Y. L., Bökenkamp, R., van Mil, A. M., Breuning, M. H., Ruivenkamp, C., ten Broeke, S. W., Veldkamp, R. F., van Waning, J. I., van Slegtenhorst, M. A., van Spaendonck-Zwarts, K. Y., Lekanne Deprez, R. H., Herkert, J. C., Boven, L., van der Zwaag, P. A., Jongbloed, J. D. H., Bootsma, M., Barge-Schaapveld, D. Q. C. M.
Published in Netherlands heart journal (01.12.2017)
Published in Netherlands heart journal (01.12.2017)
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Journal Article
Riboflavin transporter deficiency diagnosed 30 years after onset of symptoms
van der Kooi, A, Jaeger, B, van Spaendonck, K, Bosch, A
Published in Neuromuscular disorders : NMD (01.10.2016)
Published in Neuromuscular disorders : NMD (01.10.2016)
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Genetic advances in sarcomeric cardiomyopathies: state of the art
Ho, Carolyn Y, Charron, Philippe, Richard, Pascale, Girolami, Francesca, Van Spaendonck-Zwarts, Karin Y, Pinto, Yigal
Published in Cardiovascular research (01.04.2015)
Published in Cardiovascular research (01.04.2015)
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Cognitive deficits following stroke in the basal ganglia
Hochstenbach, Jacqueline, van Spaendonck, Karel PM, Cools, Alexander R, Horstink, Martin WIM, Mulder, Theo
Published in Clinical rehabilitation (01.12.1998)
Published in Clinical rehabilitation (01.12.1998)
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A live-born child with a mosaic chromosomal pattern of either monosomy 21 or trisomy 4 in different embryonal germ layers
van der Kevie-Kersemaekers, A. M. F., Suijkerbuijk, R. F., Moll, F. C. P., Dijkhuizen, T., van Spaendonck-Zwarts, K. Y., Drok, G., Bouman, K., Sikkema-Raddatz, B.
Published in Prenatal diagnosis (01.01.2010)
Published in Prenatal diagnosis (01.01.2010)
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Cognitive function in early adult and adult onset myotonic dystrophy
Van Spaendonck, K P, Ter Bruggen, J P, Weyn Banningh, E W, Maassen, B A, Van de Biezenbos, J B, Gabreëls, F J
Published in Acta neurologica Scandinavica (01.06.1995)
Published in Acta neurologica Scandinavica (01.06.1995)
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Haloperidol and cognitive shifting
Berger, H J, van Hoof, J J, van Spaendonck, K P, Horstink, M W, van den Bercken, J H, Jaspers, R, Cools, A R
Published in Neuropsychologia (1989)
Published in Neuropsychologia (1989)
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Peripartum cardiomyopathy: Euro Observational Research Program
Hoes, M. F., van Hagen, I., Russo, F., Van Veldhuisen, D. J., Van den Berg, M. P., Roos-Hesselink, J., van Spaendonck-Zwarts, K. Y., van der Meer, P.
Published in Netherlands heart journal (01.09.2014)
Published in Netherlands heart journal (01.09.2014)
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Memory and learning strategies in patients with Parkinson's disease
Buytenhuijs, E L, Berger, H J, Van Spaendonck, K P, Horstink, M W, Borm, G F, Cools, A R
Published in Neuropsychologia (01.03.1994)
Published in Neuropsychologia (01.03.1994)
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Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D
van Spaendonck-Zwarts, K. Y., van der Kooi, A. J., van den Berg, M. P., Ippel, E. F., Boven, L. G., Yee, W.-C., van den Wijngaard, A., Brusse, E., Hoogendijk, J. E., Doevendans, P. A., de Visser, M., Jongbloed, J. D. H., van Tintelen, J. P.
Published in Netherlands heart journal (01.05.2012)
Published in Netherlands heart journal (01.05.2012)
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Journal Article
Spasmodic torticollis: the problem of pathophysiology and assessment
van Hoof, J J, Horstink, M W, Berger, H J, van Spaendonck, K P, Cools, A R
Published in Journal of neurology (01.06.1987)
Published in Journal of neurology (01.06.1987)
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