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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 4
1993 3
1994 1
1995 1
1996 4
1997 1
1998 1
1999 3
2002 1
2003 1
2005 2
2006 1
2008 1
2009 1
2010 2
2012 1
2015 1
2024 0

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29 results

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Page 1
Rhombencephalosynapsis: clinical findings and neuroimaging in 9 children.
Toelle SP, Yalcinkaya C, Kocer N, Deonna T, Overweg-Plandsoen WC, Bast T, Kalmanchey R, Barsi P, Schneider JF, Capone Mori A, Boltshauser E. Toelle SP, et al. Among authors: overweg plandsoen wc. Neuropediatrics. 2002 Aug;33(4):209-14. doi: 10.1055/s-2002-34498. Neuropediatrics. 2002. PMID: 12368992 Review.
Cerebellar hypoplasia-endosteal sclerosis: a long term follow-up.
Ozgen HM, Overweg-Plandsoen WC, Blees-Pelk J, Besselaar PP, Hennekam RC. Ozgen HM, et al. Among authors: overweg plandsoen wc. Am J Med Genet A. 2005 Apr 15;134A(2):215-9. doi: 10.1002/ajmg.a.30589. Am J Med Genet A. 2005. PMID: 15672385 Review.
Non-invasive pressure monitoring in infants.
Overweg-Plandsoen WC, de Jong DA, Avezaat CJ. Overweg-Plandsoen WC, et al. Eur J Pediatr Surg. 1992 Dec;2 Suppl 1:38. Eur J Pediatr Surg. 1992. PMID: 1489748 No abstract available.
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy.
Scoto M, Rossor AM, Harms MB, Cirak S, Calissano M, Robb S, Manzur AY, Martínez Arroyo A, Rodriguez Sanz A, Mansour S, Fallon P, Hadjikoumi I, Klein A, Yang M, De Visser M, Overweg-Plandsoen WC, Baas F, Taylor JP, Benatar M, Connolly AM, Al-Lozi MT, Nixon J, de Goede CG, Foley AR, Mcwilliam C, Pitt M, Sewry C, Phadke R, Hafezparast M, Chong WK, Mercuri E, Baloh RH, Reilly MM, Muntoni F. Scoto M, et al. Among authors: overweg plandsoen wc. Neurology. 2015 Feb 17;84(7):668-79. doi: 10.1212/WNL.0000000000001269. Epub 2015 Jan 21. Neurology. 2015. PMID: 25609763 Free PMC article.
GLUT-1 deficiency without epilepsy--an exceptional case.
Overweg-Plandsoen WC, Groener JE, Wang D, Onkenhout W, Brouwer OF, Bakker HD, De Vivo DC. Overweg-Plandsoen WC, et al. J Inherit Metab Dis. 2003;26(6):559-63. doi: 10.1023/a:1025999914822. J Inherit Metab Dis. 2003. PMID: 14605501
Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study.
Ketelslegers IA, Catsman-Berrevoets CE, Neuteboom RF, Boon M, van Dijk KG, Eikelenboom MJ, Gooskens RH, Niks EH, Overweg-Plandsoen WC, Peeters EA, Peeters-Scholte CM, Poll-The BT, de Rijk-van Andel JF, Samijn JP, Snoeck IN, Stroink H, Vermeulen RJ, Verrips A, Vles JS, Willemsen MA, Rodrigues Pereira R, Hintzen RQ. Ketelslegers IA, et al. Among authors: overweg plandsoen wc. J Neurol. 2012 Sep;259(9):1929-35. doi: 10.1007/s00415-012-6441-6. Epub 2012 Feb 17. J Neurol. 2012. PMID: 22349866 Free PMC article.
Molybdenum cofactor deficiency can mimic postanoxic encephalopathy.
Bakker HD, Abeling NG, ten Houten R, van den Blij JF, Overweg-Plandsoen WC, Wanders RJ, van Gennip AH. Bakker HD, et al. Among authors: overweg plandsoen wc. J Inherit Metab Dis. 1993;16(5):900-1. doi: 10.1007/BF00714290. J Inherit Metab Dis. 1993. PMID: 8295412 No abstract available.
Intracranial hypertension in 2 children with marfan syndrome.
Hilhorst-Hofstee Y, Kroft LJ, Pals G, van Vugt JP, Overweg-Plandsoen WC. Hilhorst-Hofstee Y, et al. Among authors: overweg plandsoen wc. J Child Neurol. 2008 Aug;23(8):954-5. doi: 10.1177/0883073808315341. Epub 2008 Mar 19. J Child Neurol. 2008. PMID: 18354149
Acute motor and sensory axonal neuropathy in LEOPARD syndrome.
Beukers RJ, van Bellegem AC, Gruppen M, Overweg-Plandsoen WC, Vermeulen M. Beukers RJ, et al. Among authors: overweg plandsoen wc. Pediatr Neurol. 2010 Apr;42(4):301-3. doi: 10.1016/j.pediatrneurol.2009.12.001. Pediatr Neurol. 2010. PMID: 20304339
29 results