de Wit MC - Search Results

1

Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus.

de Wit MC, de Coo IF, Julier C, Delépine M, Lequin MH, van de Laar I, Sibbles BJ, Bruining GJ, Mancini GM. de Wit MC, et al. Among authors: de coo if. Neurogenetics. 2006 Nov;7(4):259-63. doi: 10.1007/s10048-006-0061-1. Epub 2006 Sep 14. Neurogenetics. 2006. PMID: 16972080

2

Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency.

de Wit MC, de Coo IF, Verbeek E, Schot R, Schoonderwoerd GC, Duran M, de Klerk JB, Huijmans JG, Lequin MH, Verheijen FW, Mancini GM. de Wit MC, et al. Among authors: de coo if, de klerk jb. Mol Genet Metab. 2006 Feb;87(2):102-6. doi: 10.1016/j.ymgme.2005.09.009. Epub 2005 Nov 4. Mol Genet Metab. 2006. PMID: 16275149

3

Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects.

de Wit MC, Kros JM, Halley DJ, de Coo IF, Verdijk R, Jacobs BC, Mancini GM. de Wit MC, et al. Among authors: de coo if. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):426-8. doi: 10.1136/jnnp.2008.149419. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289478

4

Movement disorder and neuronal migration disorder due to ARFGEF2 mutation.

de Wit MC, de Coo IF, Halley DJ, Lequin MH, Mancini GM. de Wit MC, et al. Among authors: de coo if. Neurogenetics. 2009 Oct;10(4):333-6. doi: 10.1007/s10048-009-0192-2. Epub 2009 Apr 22. Neurogenetics. 2009. PMID: 19384555 Free PMC article.

5

Absence epilepsy and periventricular nodular heterotopia.

de Wit MC, Schippers HM, de Coo IF, Arts WF, Lequin MH, Brooks A, Visser GH, Mancini GM. de Wit MC, et al. Among authors: de coo if. Seizure. 2010 Sep;19(7):450-2. doi: 10.1016/j.seizure.2010.06.013. Epub 2010 Jul 15. Seizure. 2010. PMID: 20637656 Free article.

6

Lung disease in FLNA mutation: confirmatory report.

de Wit MC, Tiddens HA, de Coo IF, Mancini GM. de Wit MC, et al. Among authors: de coo if. Eur J Med Genet. 2011 May-Jun;54(3):299-300. doi: 10.1016/j.ejmg.2010.12.009. Epub 2010 Dec 29. Eur J Med Genet. 2011. PMID: 21194575

7

Validated age-specific reference values for CSF total protein levels in children.

Kahlmann V, Roodbol J, van Leeuwen N, Ramakers CRB, van Pelt D, Neuteboom RF, Catsman-Berrevoets CE, de Wit MCY, Jacobs BC. Kahlmann V, et al. Eur J Paediatr Neurol. 2017 Jul;21(4):654-660. doi: 10.1016/j.ejpn.2017.03.006. Epub 2017 Apr 8. Eur J Paediatr Neurol. 2017. PMID: 28461111

8

Acute flaccid myelitis and Guillain-Barré syndrome in children: A comparative study with evaluation of diagnostic criteria.

Helfferich J, Roodbol J, de Wit MC, Brouwer OF, Jacobs BC; 2016 Enterovirus D68 Acute Flaccid Myelitis Working Group and the Dutch Pediatric GBS Study Group. Helfferich J, et al. Among authors: de wit mc. Eur J Neurol. 2022 Feb;29(2):593-604. doi: 10.1111/ene.15170. Epub 2021 Nov 24. Eur J Neurol. 2022. PMID: 34747551 Free PMC article.

9

Recognizing Guillain-Barre syndrome in preschool children.

Roodbol J, de Wit MC, Walgaard C, de Hoog M, Catsman-Berrevoets CE, Jacobs BC. Roodbol J, et al. Among authors: de wit mc, de hoog m. Neurology. 2011 Mar 1;76(9):807-10. doi: 10.1212/WNL.0b013e31820e7b62. Neurology. 2011. PMID: 21357832

10

Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complex.

Overwater IE, Verhaar BJ, Lingsma HF, Bindels-de Heus GC, van den Ouweland AM, Nellist M, Ten Hoopen LW, Elgersma Y, Moll HA, de Wit MC. Overwater IE, et al. Among authors: de wit mc. J Neurol. 2017 Jan;264(1):161-167. doi: 10.1007/s00415-016-8335-5. Epub 2016 Nov 22. J Neurol. 2017. PMID: 27878438 Free PMC article.

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