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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
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
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.
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
87 results