van der Knaap MS - Search Results

1

Reply: TUBB4A novel mutation reinforces the genotype-phenotype correlation of hypomyelination with atrophy of the basal ganglia and cerebellum.

Hamilton EM, Wolf NI, van der Knaap MS. Hamilton EM, et al. Among authors: van der knaap ms. Brain. 2015 Feb;138(Pt 2):e328. doi: 10.1093/brain/awu243. Epub 2014 Aug 27. Brain. 2015. PMID: 25168211 No abstract available.

2

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.

3

Severe hypomyelination associated with increased levels of N-acetylaspartylglutamate in CSF.

Wolf NI, Willemsen MA, Engelke UF, van der Knaap MS, Pouwels PJ, Harting I, Zschocke J, Sistermans EA, Rating D, Wevers RA. Wolf NI, et al. Among authors: van der knaap ms. Neurology. 2004 May 11;62(9):1503-8. doi: 10.1212/01.wnl.0000123094.13406.20. Neurology. 2004. PMID: 15136672

4

Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathology.

van der Knaap MS, Linnankivi T, Paetau A, Feigenbaum A, Wakusawa K, Haginoya K, Köhler W, Henneke M, Dinopoulos A, Grattan-Smith P, Brockmann K, Schiffmann R, Blaser S. van der Knaap MS, et al. Neurology. 2007 Jul 10;69(2):166-71. doi: 10.1212/01.wnl.0000265592.74483.a6. Neurology. 2007. PMID: 17620549

5

AGC1 deficiency and cerebral hypomyelination.

Wolf NI, van der Knaap MS. Wolf NI, et al. Among authors: van der knaap ms. N Engl J Med. 2009 Nov 12;361(20):1997-8; author reply 1998. doi: 10.1056/NEJMc091723. N Engl J Med. 2009. PMID: 19907050 No abstract available.

6

Megalencephalic leukoencephalopathy with cysts without MLC1 defect.

van der Knaap MS, Lai V, Köhler W, Salih MA, Fonseca MJ, Benke TA, Wilson C, Jayakar P, Aine MR, Dom L, Lynch B, Kálmánchey R, Pietsch P, Errami A, Scheper GC. van der Knaap MS, et al. Ann Neurol. 2010 Jun;67(6):834-7. doi: 10.1002/ana.21980. Ann Neurol. 2010. PMID: 20517947

7

Hypomyelination versus delayed myelination.

van der Knaap MS, Wolf NI. van der Knaap MS, et al. Ann Neurol. 2010 Jul;68(1):115. doi: 10.1002/ana.21751. Ann Neurol. 2010. PMID: 20582949 No abstract available.

8

Magnetic resonance imaging pattern recognition in hypomyelinating disorders.

Steenweg ME, Vanderver A, Blaser S, Bizzi A, de Koning TJ, Mancini GM, van Wieringen WN, Barkhof F, Wolf NI, van der Knaap MS. Steenweg ME, et al. Among authors: van wieringen wn, van der knaap ms. Brain. 2010 Oct;133(10):2971-82. doi: 10.1093/brain/awq257. Brain. 2010. PMID: 20881161 Free PMC article.

9

Genotype-phenotype correlation in vanishing white matter disease.

van der Lei HD, van Berkel CG, van Wieringen WN, Brenner C, Feigenbaum A, Mercimek-Mahmutoglu S, Philippart M, Tatli B, Wassmer E, Scheper GC, van der Knaap MS. van der Lei HD, et al. Among authors: van wieringen wn, van berkel cg, van der knaap ms. Neurology. 2010 Oct 26;75(17):1555-9. doi: 10.1212/WNL.0b013e3181f962ae. Neurology. 2010. PMID: 20975056

10

Hypomyelination with atrophy of the basal ganglia and cerebellum in an infant with Down syndrome.

Narumi Y, Shiihara T, Yoshihashi H, Sakazume S, van der Knaap MS, Nishimura-Tadaki A, Matsumoto N, Fukushima Y. Narumi Y, et al. Among authors: van der knaap ms. Clin Dysmorphol. 2011 Jul;20(3):166-167. doi: 10.1097/MCD.0b013e32834659a8. Clin Dysmorphol. 2011. PMID: 21471810 No abstract available.

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