Chemokine induction by all-trans retinoic acid and arsenic trioxide in acute promyelocytic leukemia: triggering the differentiation syndrome
Luesink, Maaike, Pennings, Jeroen L.A., Wissink, Willemijn M., Linssen, Peter C.M., Muus, Petra, Pfundt, Rolph, de Witte, Theo J.M., van der Reijden, Bert A., Jansen, Joop H.
Published in Blood (24.12.2009)
Published in Blood (24.12.2009)
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B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies
Maroofian, Reza, Riemersma, Moniek, Jae, Lucas T, Zhianabed, Narges, Willemsen, Marjolein H, Wissink-Lindhout, Willemijn M, Willemsen, Michèl A, de Brouwer, Arjan P M, Mehrjardi, Mohammad Yahya Vahidi, Ashrafi, Mahmoud Reza, Kusters, Benno, Kleefstra, Tjitske, Jamshidi, Yalda, Nasseri, Mojila, Pfundt, Rolph, Brummelkamp, Thijn R, Abbaszadegan, Mohammad Reza, Lefeber, Dirk J, van Bokhoven, Hans
Published in Genome medicine (22.12.2017)
Published in Genome medicine (22.12.2017)
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Homozygous SLC6A17 Mutations Cause Autosomal-Recessive Intellectual Disability with Progressive Tremor, Speech Impairment, and Behavioral Problems
Iqbal, Zafar, Willemsen, Marjolein H., Papon, Marie-Amélie, Musante, Luciana, Benevento, Marco, Hu, Hao, Venselaar, Hanka, Wissink-Lindhout, Willemijn M., Vulto-van Silfhout, Anneke T., Vissers, Lisenka E.L.M., de Brouwer, Arjan P.M., Marouillat, Sylviane, Wienker, Thomas F., Ropers, Hans Hilger, Kahrizi, Kimia, Nadif Kasri, Nael, Najmabadi, Hossein, Laumonnier, Frédéric, Kleefstra, Tjitske, van Bokhoven, Hans
Published in American journal of human genetics (05.03.2015)
Published in American journal of human genetics (05.03.2015)
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Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function
Willemsen, Marjolein H, Ba, Wei, Wissink-Lindhout, Willemijn M, de Brouwer, Arjan P M, Haas, Stefan A, Bienek, Melanie, Hu, Hao, Vissers, Lisenka E L M, van Bokhoven, Hans, Kalscheuer, Vera, Nadif Kasri, Nael, Kleefstra, Tjitske
Published in Journal of medical genetics (01.07.2014)
Published in Journal of medical genetics (01.07.2014)
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Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability
Willemsen, Marjolein H, Vallès, Astrid, Kirkels, Laurens A M H, Mastebroek, Mathilde, Olde Loohuis, Nikkie, Kos, Aron, Wissink-Lindhout, Willemijn M, de Brouwer, Arjan P M, Nillesen, Willy M, Pfundt, Rolph, Holder-Espinasse, Muriel, Vallée, Louis, Andrieux, Joris, Coppens-Hofman, Marjolein C, Rensen, Hanneke, Hamel, Ben C J, van Bokhoven, Hans, Aschrafi, Armaz, Kleefstra, Tjitske
Published in Journal of medical genetics (01.12.2011)
Published in Journal of medical genetics (01.12.2011)
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Interferon‐γ‐based mixed lymphocyte culture as a selection tool for allogeneic bone marrow donors other than identical siblings
Van Der Meer, Arnold, Wissink, Willemijn M., Schattenberg, Anton V. M. B., Joosten, Irma
Published in British journal of haematology (01.05.1999)
Published in British journal of haematology (01.05.1999)
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Chromosome 1p21.3 microdeletions comprising DPYD and MIR 137 are associated with intellectual disability
WILLEMSEN, Marjolein H, VALLES, Astrid, HOLDER-ESPINASSE, Muriel, VALLEE, Louis, ANDRIEUX, Joris, COPPENS-HOFMAN, Marjolein C, RENSEN, Hanneke, HAMEL, Ben C. J, VAN BOKHOVEN, Hans, ASCHRAFI, Armaz, KLEEFSTRA, Tjitske, KIRKELS, Laurens A.m H, MASTEBROEK, Mathilde, OLDE LOOHUIS, Nikkie, KOS, Aron, WISSINK-LINDHOUT, Willemijn M, DE BROUWER, Arian P. M, NILLESEN, Willy M, PFUNDT, Rolph
Published in Journal of medical genetics (2011)
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Published in Journal of medical genetics (2011)
Journal Article
MLC reactivity can be further differentiated by cytokine measurements
Wissink, Willemijn M., van der Meer, Arnold, Ruiter, Jos, Allebes, Wil, Joosten, Irma
Published in Immunology letters (01.05.1997)
Published in Immunology letters (01.05.1997)
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