van der Knaap MS - Search Results

1

Update on Leukodystrophies: A Historical Perspective and Adapted Definition.

Kevelam SH, Steenweg ME, Srivastava S, Helman G, Naidu S, Schiffmann R, Blaser S, Vanderver A, Wolf NI, van der Knaap MS. Kevelam SH, et al. Among authors: van der knaap ms. Neuropediatrics. 2016 Dec;47(6):349-354. doi: 10.1055/s-0036-1588020. Epub 2016 Aug 26. Neuropediatrics. 2016. PMID: 27564080 Review.

2

Cortical laminar abnormalities--occurrence and clinical significance.

van der Knaap MS, Smit LS, Nauta JJ, Lafeber HN, Valk J. van der Knaap MS, et al. Neuropediatrics. 1993 Jun;24(3):143-8. doi: 10.1055/s-2008-1071532. Neuropediatrics. 1993. PMID: 8355819

3

Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach.

van der Knaap MS, Breiter SN, Naidu S, Hart AA, Valk J. van der Knaap MS, et al. Radiology. 1999 Oct;213(1):121-33. doi: 10.1148/radiology.213.1.r99se01121. Radiology. 1999. PMID: 10540652

4

Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids.

van der Knaap MS, Naidu S, Kleinschmidt-Demasters BK, Kamphorst W, Weinstein HC. van der Knaap MS, et al. Neurology. 2000 Jan 25;54(2):463-8. doi: 10.1212/wnl.54.2.463. Neurology. 2000. PMID: 10668715

5

Alexander disease: diagnosis with MR imaging.

van der Knaap MS, Naidu S, Breiter SN, Blaser S, Stroink H, Springer S, Begeer JC, van Coster R, Barth PG, Thomas NH, Valk J, Powers JM. van der Knaap MS, et al. Among authors: van coster r. AJNR Am J Neuroradiol. 2001 Mar;22(3):541-52. AJNR Am J Neuroradiol. 2001. PMID: 11237983 Free PMC article.

6

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

Leegwater PA, Vermeulen G, Könst AA, Naidu S, Mulders J, Visser A, Kersbergen P, Mobach D, Fonds D, van Berkel CG, Lemmers RJ, Frants RR, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS. Leegwater PA, et al. Among authors: van berkel cg, van der knaap ms. Nat Genet. 2001 Dec;29(4):383-8. doi: 10.1038/ng764. Nat Genet. 2001. PMID: 11704758

7

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.

van der Knaap MS, Leegwater PA, Könst AA, Visser A, Naidu S, Oudejans CB, Schutgens RB, Pronk JC. van der Knaap MS, et al. Ann Neurol. 2002 Feb;51(2):264-70. doi: 10.1002/ana.10112. Ann Neurol. 2002. PMID: 11835386

8

Molecular findings in symptomatic and pre-symptomatic Alexander disease patients.

Gorospe JR, Naidu S, Johnson AB, Puri V, Raymond GV, Jenkins SD, Pedersen RC, Lewis D, Knowles P, Fernandez R, De Vivo D, van der Knaap MS, Messing A, Brenner M, Hoffman EP. Gorospe JR, et al. Among authors: van der knaap ms. Neurology. 2002 May 28;58(10):1494-500. doi: 10.1212/wnl.58.10.1494. Neurology. 2002. PMID: 12034785

9

New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.

van der Knaap MS, Naidu S, Pouwels PJ, Bonavita S, van Coster R, Lagae L, Sperner J, Surtees R, Schiffmann R, Valk J. van der Knaap MS, et al. Among authors: van coster r. AJNR Am J Neuroradiol. 2002 Oct;23(9):1466-74. AJNR Am J Neuroradiol. 2002. PMID: 12372733 Free PMC article.

10

A new leukoencephalopathy with brainstem and spinal cord involvement and high lactate.

van der Knaap MS, van der Voorn P, Barkhof F, Van Coster R, Krägeloh-Mann I, Feigenbaum A, Blaser S, Vles JS, Rieckmann P, Pouwels PJ. van der Knaap MS, et al. Among authors: van der voorn p, van coster r. Ann Neurol. 2003 Feb;53(2):252-8. doi: 10.1002/ana.10456. Ann Neurol. 2003. PMID: 12557294

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