van der Knaap M - Search Results

1

No evidence that polymorphisms of the vanishing white matter disease genes are risk factors in multiple sclerosis.

Pronk J, Scheper G, van Andel R, van Berkel C, Polman Ch, Uitdehaag B, van der Knaap M. Pronk J, et al. Among authors: van berkel c, van andel r, van der knaap m. Mult Scler. 2008 Sep;14(8):1123-6. doi: 10.1177/1352458508093618. Epub 2008 Jul 16. Mult Scler. 2008. PMID: 18632786

2

Vanishing white matter disease associated with progressive macrocephaly.

Pineda M, R-Palmero A, Baquero M, O'Callaghan M, Aracil A, van der Knaap M, Scheper GC. Pineda M, et al. Among authors: van der knaap m. Neuropediatrics. 2008 Feb;39(1):29-32. doi: 10.1055/s-2008-1076738. Neuropediatrics. 2008. PMID: 18504679

3

Bergmann glia translocation: a new disease marker for vanishing white matter identifies therapeutic effects of Guanabenz treatment.

Dooves S, Bugiani M, Wisse LE, Abbink TEM, van der Knaap MS, Heine VM. Dooves S, et al. Among authors: van der knaap ms. Neuropathol Appl Neurobiol. 2018 Jun;44(4):391-403. doi: 10.1111/nan.12411. Epub 2017 Aug 1. Neuropathol Appl Neurobiol. 2018. PMID: 28953319

4

A child with macrocephaly: case report of a patient with megalencephalic leukoencephalopathy with subcortical cysts and a compound heterozygosity for two mutations in the MLC1 gene.

Delmonaco AG, Gaidolfi E, Scheper GC, Girardo E, Molinatto C, Belligni E, Ferrero GB, Cirillo Silengo M, Van Der Knaap M. Delmonaco AG, et al. Among authors: van der knaap m. Minerva Pediatr. 2011 Apr;63(2):125-9. Minerva Pediatr. 2011. PMID: 21487377

5

Translation initiation factor eIF2Bε promotes Wnt-mediated clonogenicity and global translation in intestinal epithelial cells.

Smit WL, de Boer RJ, Meijer BJ, Spaan CN, van Roest M, Koelink PJ, Koster J, Dekker E, Abbink TEM, van der Knaap MS, van den Brink GR, Muncan V, Heijmans J. Smit WL, et al. Among authors: van roest m, van den brink gr, van der knaap ms. Stem Cell Res. 2021 Aug;55:102499. doi: 10.1016/j.scr.2021.102499. Epub 2021 Aug 11. Stem Cell Res. 2021. PMID: 34399164 Free article.

6

Plasmacytoid dendritic cells and interferon-alpha in Aicardi-Goutières syndrome.

van Heteren JT, van der Knaap MS, Poll The BW, Kuijpers TW. van Heteren JT, et al. Among authors: van der knaap ms. Neuropediatrics. 2007 Dec;38(6):269-75. doi: 10.1055/s-2008-1065352. Neuropediatrics. 2007. PMID: 18461501

7

Kearns-Sayre syndrome with a phenocopy of choroideremia instead of pigmentary retinopathy.

Herzberg NH, van Schooneveld MJ, Bleeker-Wagemakers EM, Zwart R, Cremers FP, van der Knaap MS, Bolhuis PA, de Visser M. Herzberg NH, et al. Among authors: van schooneveld mj, van der knaap ms. Neurology. 1993 Jan;43(1):218-21. doi: 10.1212/wnl.43.1_part_1.218. Neurology. 1993. PMID: 8423892

8

Hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC). Report of a new case.

Mercimek-Mahmutoglu S, van der Knaap MS, Baric I, Prayer D, Stoeckler-Ipsiroglu S. Mercimek-Mahmutoglu S, et al. Among authors: van der knaap ms. Neuropediatrics. 2005 Jun;36(3):223-6. doi: 10.1055/s-2005-865715. Neuropediatrics. 2005. PMID: 15944912

9

Megalencephalic Leukoencephalopathy With Subcortical Cysts in an Adult.

Bartsch AJ, van der Knaap M. Bartsch AJ, et al. Among authors: van der knaap m. Dtsch Arztebl Int. 2024 Oct 18;121(21):702. doi: 10.3238/arztebl.m2024.0086. Dtsch Arztebl Int. 2024. PMID: 39841498 No abstract available.

10

Optimising diagnostics for hard-of-hearing infants: factors associated with successful MRI scanning without general anaesthesia.

van der Veen MD, Kaman I, Jasperse B, Goderie T, Ebbens FA, Slot KM, van der Knaap MS, Merkus P. van der Veen MD, et al. Among authors: van der knaap ms. Eur Arch Otorhinolaryngol. 2025 Jan 17. doi: 10.1007/s00405-024-09118-6. Online ahead of print. Eur Arch Otorhinolaryngol. 2025. PMID: 39825196

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