Patients with obesity have more inflamed joints and higher CRP levels during the disease course in ACPA-positive RA but not in ACPA-negative RA
Hollander, N K den, Boeren, A M P, van der Helm-van Mil, A H M, van Steenbergen, H W
Published in Arthritis research & therapy (07.02.2024)
Published in Arthritis research & therapy (07.02.2024)
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Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
Halgren, C, Kjaergaard, S, Bak, M, Hansen, C, El-Schich, Z, Anderson, CM, Henriksen, KF, Hjalgrim, H, Kirchhoff, M, Bijlsma, EK, Nielsen, M, den Hollander, NS, Ruivenkamp, CAL, Isidor, B, Le Caignec, C, Zannolli, R, Mucciolo, M, Renieri, A, Mari, F, Anderlid, B-M, Andrieux, J, Dieux, A, Tommerup, N, Bache, I
Published in Clinical genetics (01.09.2012)
Published in Clinical genetics (01.09.2012)
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Journal Article
Further delineation of Pitt–Hopkins syndrome: phenotypic and genotypic description of 16 novel patients
Zweier, C, Sticht, H, Bijlsma, E K, Clayton-Smith, J, Boonen, S E, Fryer, A, Greally, M T, Hoffmann, L, den Hollander, N S, Jongmans, M, Kant, S G, King, M D, Lynch, S A, McKee, S, Midro, A T, Park, S-M, Ricotti, V, Tarantino, E, Wessels, M, Peippo, M, Rauch, A
Published in Journal of medical genetics (01.11.2008)
Published in Journal of medical genetics (01.11.2008)
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Journal Article
Advanced glycation end products and the absence of premature atherosclerosis in glycogen storage disease Ia
den Hollander, N. C, Mulder, D. J, Graaff, R, Thorpe, S. R, Baynes, J. W, Smit, G. P. A, Smit, A. J
Published in Journal of inherited metabolic disease (01.11.2007)
Published in Journal of inherited metabolic disease (01.11.2007)
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Disentangling heterogeneity in contemporary undifferentiated arthritis - A large cohort study using latent class analysis
den Hollander, N K, Verstappen, M, van Dijk, B T, van der Helm-van Mil, A H M, van Steenbergen, H W
Published in Seminars in arthritis and rheumatism (01.12.2023)
Published in Seminars in arthritis and rheumatism (01.12.2023)
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Journal Article
X-chromosome duplications in males with mental retardation: pathogenic or benign variants?
Gijsbers, ACJ, Den Hollander, NS, Helderman-van de Enden, ATJM, Schuurs-Hoeijmakers, JHM, Vijfhuizen, L, Bijlsma, EK, Van Haeringen, A, Hansson, KBM, Bakker, E, Breuning, MH, Ruivenkamp, CAL
Published in Clinical genetics (01.01.2011)
Published in Clinical genetics (01.01.2011)
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Journal Article
Early prenatal sonographic diagnosis and follow‐up of Jeune syndrome
Den Hollander, N. S., Robben, S. G. F., Hoogeboom, A. J. M., Niermeijer, M. F., Wladimiroff, J. W.
Published in Ultrasound in obstetrics & gynecology (01.10.2001)
Published in Ultrasound in obstetrics & gynecology (01.10.2001)
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Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting
Goobie, S., Knijnenburg, J., FitzPatrick, D., Sharkey, F.H., Lionel, A.C., Marshall, C.R., Azam, T., Shago, M., Chong, K., Mendoza-Londono, R., den Hollander, N.S., Ruivenkamp, C., Maher, E., Tanke, H.J., Szuhai, K., Wintle, R.F., Scherer, S.W.
Published in Cytogenetic and genome research (01.01.2008)
Published in Cytogenetic and genome research (01.01.2008)
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Early fetal anomaly scanning in a population at increased risk of abnormalities
Den Hollander, N. S., Wessels, M. W., Niermeijer, M. F., Los, F. J., Wladimiroff, J. W.
Published in Ultrasound in obstetrics & gynecology (01.06.2002)
Published in Ultrasound in obstetrics & gynecology (01.06.2002)
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Journal Article
Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia
Sung, L., Dix, D., Cellot, S., Gillmeister, B., Ethier, M.C., Roslin, N.M., Johnston, D.L., Feusner, J., Mitchell, D., Lewis, V., Aplenc, R., Yanofsky, R., Portwine, C., Price, V., Zelcer, S., Silva, M., Bowes, L., Michon, B., Stobart, K., Traubici, J., Allen, U., Beyene, J., den Hollander, N., Paterson, A.D.
Published in Clinical microbiology and infection (01.06.2016)
Published in Clinical microbiology and infection (01.06.2016)
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In‐utero diagnosis of mucopolysaccharidosis type VII in a fetus with an enlarged nuchal translucency
Den Hollander, N. S., Kleijer, W. J., Schoonderwaldt, E. M., Los, F. J., Wladimiroff, J. W., Niermeijer, M. F.
Published in Ultrasound in obstetrics & gynecology (01.07.2000)
Published in Ultrasound in obstetrics & gynecology (01.07.2000)
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Prenatal diagnosis of type A1 brachydactyly
Den Hollander, N. S., Hoogeboom, A. J. M., Niermeijer, M. F., Wladimiroff, J. W.
Published in Ultrasound in obstetrics & gynecology (01.06.2001)
Published in Ultrasound in obstetrics & gynecology (01.06.2001)
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Journal Article
Congenital Disorder of Glycosylation type Ia presenting with hydrops fetalis
van de Kamp, Jiddeke Matuja, Lefeber, Dirk J, Ruijter, George JG, Steggerda, Sylke J, den Hollander, Nicolette S, Willems, Stefan M, Matthijs, Gert, Poorthuis, Ben JHM, Wevers, Ron A
Published in Journal of medical genetics (01.04.2007)
Published in Journal of medical genetics (01.04.2007)
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Journal Article
Prenatal diagnosis of congenital diaphragmatic hernia: a retrospective analysis of 28 cases
Manni, M, Heydanus, R, Den Hollander, N S, Stewart, P A, De Vogelaere, C, Wladimiroff, J W
Published in Prenatal diagnosis (01.03.1994)
Published in Prenatal diagnosis (01.03.1994)
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