Küsters B - Search Results

1

TDP-43 accumulation is common in myopathies with rimmed vacuoles.

Küsters B, van Hoeve BJ, Schelhaas HJ, Ter Laak H, van Engelen BG, Lammens M. Küsters B, et al. Acta Neuropathol. 2009 Feb;117(2):209-11. doi: 10.1007/s00401-008-0471-2. Epub 2008 Dec 9. Acta Neuropathol. 2009. PMID: 19066918 No abstract available.

2

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations.

Seelaar H, Schelhaas HJ, Azmani A, Küsters B, Rosso S, Majoor-Krakauer D, de Rijk MC, Rizzu P, ten Brummelhuis M, van Doorn PA, Kamphorst W, Willemsen R, van Swieten JC. Seelaar H, et al. Among authors: kusters b. Brain. 2007 May;130(Pt 5):1375-85. doi: 10.1093/brain/awm024. Epub 2007 Mar 14. Brain. 2007. PMID: 17360763 Free article.

3

Sulfation of heparan sulfate associated with amyloid-beta plaques in patients with Alzheimer's disease.

Bruinsma IB, te Riet L, Gevers T, ten Dam GB, van Kuppevelt TH, David G, Küsters B, de Waal RM, Verbeek MM. Bruinsma IB, et al. Among authors: kusters b. Acta Neuropathol. 2010 Feb;119(2):211-20. doi: 10.1007/s00401-009-0577-1. Epub 2009 Jul 28. Acta Neuropathol. 2010. PMID: 19636575

4

Activating mutations of the GNAQ gene: a frequent event in primary melanocytic neoplasms of the central nervous system.

Küsters-Vandevelde HV, Klaasen A, Küsters B, Groenen PJ, van Engen-van Grunsven IA, van Dijk MR, Reifenberger G, Wesseling P, Blokx WA. Küsters-Vandevelde HV, et al. Among authors: kusters b. Acta Neuropathol. 2010 Mar;119(3):317-23. doi: 10.1007/s00401-009-0611-3. Acta Neuropathol. 2010. PMID: 19936769 Free PMC article.

5

Improved discrimination of melanotic schwannoma from melanocytic lesions by combined morphological and GNAQ mutational analysis.

Küsters-Vandevelde HV, van Engen-van Grunsven IA, Küsters B, van Dijk MR, Groenen PJ, Wesseling P, Blokx WA. Küsters-Vandevelde HV, et al. Among authors: kusters b. Acta Neuropathol. 2010 Dec;120(6):755-64. doi: 10.1007/s00401-010-0749-z. Epub 2010 Sep 24. Acta Neuropathol. 2010. PMID: 20865267 Free PMC article. Review.

6

Mitochondrial enzymes discriminate between mitochondrial disorders and chronic fatigue syndrome.

Smits B, van den Heuvel L, Knoop H, Küsters B, Janssen A, Borm G, Bleijenberg G, Rodenburg R, van Engelen B. Smits B, et al. Among authors: kusters b. Mitochondrion. 2011 Sep;11(5):735-8. doi: 10.1016/j.mito.2011.05.005. Epub 2011 Jun 2. Mitochondrion. 2011. PMID: 21664495

7

Histological abnormalities induced by the electromyography needle.

Voermans NC, Sie LT, van Alfen N, van Engelen BG, Küsters B. Voermans NC, et al. Among authors: kusters b. Neuromuscul Disord. 2014 Jan;24(1):77-8. doi: 10.1016/j.nmd.2013.09.006. Epub 2013 Sep 15. Neuromuscul Disord. 2014. PMID: 24238661 No abstract available.

8

LAMA2 mutations in adult-onset muscular dystrophy with leukoencephalopathy.

Kevelam SH, van Engelen BG, van Berkel CG, Küsters B, van der Knaap MS. Kevelam SH, et al. Among authors: kusters b. Muscle Nerve. 2014 Apr;49(4):616-7. doi: 10.1002/mus.24147. Epub 2014 Feb 10. Muscle Nerve. 2014. PMID: 24327385 No abstract available.

9

Experimental treatment of NRAS-mutated neurocutaneous melanocytosis with MEK162, a MEK-inhibitor.

Küsters-Vandevelde HV, Willemsen AE, Groenen PJ, Küsters B, Lammens M, Wesseling P, Djafarihamedani M, Rijntjes J, Delye H, Willemsen MA, van Herpen CM, Blokx WA. Küsters-Vandevelde HV, et al. Among authors: kusters b. Acta Neuropathol Commun. 2014 Apr 8;2:41. doi: 10.1186/2051-5960-2-41. Acta Neuropathol Commun. 2014. PMID: 24713450 Free PMC article.

10

Fever-induced recurrent rhabdomyolysis due to a novel mutation in the ryanodine receptor type 1 gene.

Molenaar JP, Voermans NC, van Hoeve BJ, Kamsteeg EJ, Kluijtmans LA, Kusters B, Jungbluth HJ, van Engelen BG. Molenaar JP, et al. Among authors: kusters b. Intern Med J. 2014 Aug;44(8):819-20. doi: 10.1111/imj.12498. Intern Med J. 2014. PMID: 25081049 No abstract available.

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