van der Knaap MS - Search Results

1

Natural History of Vanishing White Matter.

Hamilton EMC, van der Lei HDW, Vermeulen G, Gerver JAM, Lourenço CM, Naidu S, Mierzewska H, Gemke RJBJ, de Vet HCW, Uitdehaag BMJ, Lissenberg-Witte BI; VWM Research Group; van der Knaap MS. Hamilton EMC, et al. Among authors: van der lei hdw, van der knaap ms. Ann Neurol. 2018 Aug;84(2):274-288. doi: 10.1002/ana.25287. Epub 2018 Sep 6. Ann Neurol. 2018. PMID: 30014503 Free PMC article.

2

Leukoencephalopathy with swelling and a discrepantly mild clinical course in eight children.

van der Knaap MS, Barth PG, Stroink H, van Nieuwenhuizen O, Arts WF, Hoogenraad F, Valk J. van der Knaap MS, et al. Among authors: van nieuwenhuizen o. Ann Neurol. 1995 Mar;37(3):324-34. doi: 10.1002/ana.410370308. Ann Neurol. 1995. PMID: 7695231

3

Leber's hereditary optic neuropathy with the 11 778 mtDNA mutation and white matter disease resembling multiple sclerosis: clinical, MRI and MRS findings.

Jansen PH, van der Knaap MS, de Coo IF. Jansen PH, et al. Among authors: van der knaap ms. J Neurol Sci. 1996 Feb;135(2):176-80. doi: 10.1016/0022-510x(95)00287-c. J Neurol Sci. 1996. PMID: 8867076

4

A new leukoencephalopathy with vanishing white matter.

van der Knaap MS, Barth PG, Gabreëls FJ, Franzoni E, Begeer JH, Stroink H, Rotteveel JJ, Valk J. van der Knaap MS, et al. Neurology. 1997 Apr;48(4):845-55. doi: 10.1212/wnl.48.4.845. Neurology. 1997. PMID: 9109866 Free article.

5

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.

van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J. van der Knaap MS, et al. Ann Neurol. 1997 Jul;42(1):50-9. doi: 10.1002/ana.410420110. Ann Neurol. 1997. PMID: 9225685

6

Phenotypic variation in leukoencephalopathy with vanishing white matter.

van der Knaap MS, Kamphorst W, Barth PG, Kraaijeveld CL, Gut E, Valk J. van der Knaap MS, et al. Neurology. 1998 Aug;51(2):540-7. doi: 10.1212/wnl.51.2.540. Neurology. 1998. PMID: 9710032 Clinical Trial.

7

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?

van der Knaap MS, Jakobs C, Hoffmann GF, Nyhan WL, Renier WO, Smeitink JA, Catsman-Berrevoets CE, Hjalmarson O, Vallance H, Sugita K, Bowe CM, Herrin JT, Craigen WJ, Buist NR, Brookfield DS, Chalmers RA. van der Knaap MS, et al. Ann Neurol. 1999 Jan;45(1):111-9. doi: 10.1002/1531-8249(199901)45:1<111::aid-art17>3.0.co;2-n. Ann Neurol. 1999. PMID: 9894884

8

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

9

Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter.

van der Knaap MS, Wevers RA, Kure S, Gabreëls FJ, Verhoeven NM, van Raaij-Selten B, Jaeken J. van der Knaap MS, et al. Among authors: van raaij selten b. J Child Neurol. 1999 Nov;14(11):728-31. doi: 10.1177/088307389901401108. J Child Neurol. 1999. PMID: 10593550

10

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

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