Chantal Ceuterick
Overview
Explore the profile of Chantal Ceuterick including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
486
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Recent Articles
1.
Verhoeven K, Claeys K, Zuchner S, Schroder J, Weis J, Ceuterick C, et al.
Brain
. 2006 May;
129(Pt 8):2093-102.
PMID: 16714318
Mutations in mitofusin 2 (MFN2) have been reported in Charcot-Marie-Tooth type 2 (CMT2) families. To study the distribution of mutations in MFN2 we screened 323 families and isolated patients with...
2.
Pirici D, Vandenberghe R, Rademakers R, Dermaut B, Cruts M, Vennekens K, et al.
J Neuropathol Exp Neurol
. 2006 May;
65(3):289-301.
PMID: 16651890
The most common histologic feature in patients with frontotemporal lobar degeneration (FTLD) is intracellular brain inclusions of yet uncharacterized proteins that react with antiubiquitin (Ub) antibodies, but not with tau...
3.
Verpoorten N, Verhoeven K, Weckx S, Jacobs A, Serneels S, Del Favero J, et al.
Mol Cell Neurosci
. 2005 Sep;
30(3):316-25.
PMID: 16139508
We performed differential gene expression profiling in the peripheral nervous system by comparing the transcriptome of sensory neurons with the transcriptome of lower motor neurons. Using suppression subtractive cDNA hybridization,...
4.
Kumar-Singh S, Pirici D, McGowan E, Serneels S, Ceuterick C, Hardy J, et al.
Am J Pathol
. 2005 Jul;
167(2):527-43.
PMID: 16049337
Occurrence of amyloid beta (Abeta) dense-core plaques in the brain is one of the chief hallmarks of Alzheimer's disease (AD). It is not yet clear what factors are responsible for...
5.
Wuyts W, Reyniers E, Ceuterick C, Storm K, de Barsy T, Martin J
Am J Med Genet A
. 2005 Jan;
133A(1):82-4.
PMID: 15637709
Phosphorylase kinase (PhK) deficiency is the underlying cause of variable clinical symptoms depending on the tissues involved. Until today, only a few cases of myopathy associated with muscle PhK deficiency...
6.
Nijssen P, Ceuterick C, van Diggelen O, Elleder M, Martin J, Teepen J, et al.
Brain Pathol
. 2003 Dec;
13(4):574-81.
PMID: 14655761
We describe the neuropathological and biochemical autopsy findings in 3 patients with autosomal dominant adult neuronal ceroid lipofuscinosis (ANCL, Parry type; MIM 162350), from a family with 6 affected individuals...
7.
Ammar N, Nelis E, Merlini L, Barisic N, Amouri R, Ceuterick C, et al.
Neuromuscul Disord
. 2003 Oct;
13(9):720-8.
PMID: 14561495
Mutations in the ganglioside-induced differentiation-associated protein 1 gene cause either autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A or autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis. We sequenced the...
8.
Verhoeven K, De Jonghe P, van de Putte T, Nelis E, Zwijsen A, Verpoorten N, et al.
Am J Hum Genet
. 2003 Sep;
73(4):926-32.
PMID: 14508709
Slowed nerve-conduction velocities (NCVs) are a biological endophenotype in the majority of the hereditary motor and sensory neuropathies (HMSN). Here, we identified a family with autosomal dominant segregation of slowed...
9.
Van Goethem G, Lofgren A, Dermaut B, Ceuterick C, Martin J, Van Broeckhoven C
Hum Mutat
. 2003 Jul;
22(2):175-6.
PMID: 12872260
No abstract available.
10.
Kumar-Singh S, Julliams A, Nuydens R, Ceuterick C, Labeur C, Serneels S, et al.
Neurobiol Dis
. 2002 Dec;
11(2):330-40.
PMID: 12505425
Mutations in the beta-amyloid (Abeta) sequence of the amyloid precursor protein gene (APP) present with variable disease phenotypes. While patients with the Dutch APP mutation (E693Q) have predominantly hemorrhagic strokes,...