E R Brunt
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Explore the profile of E R Brunt including associated specialties, affiliations and a list of published articles.
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41
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1150
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Recent Articles
1.
Seidel K, Siswanto S, Fredrich M, Bouzrou M, Brunt E, van Leeuwen F, et al.
Neuropathol Appl Neurobiol
. 2015 Jun;
42(2):153-66.
PMID: 26095752
Aims: Polyglutamine (polyQ) diseases are characterized by the expansion of a polymorphic glutamine sequence in disease-specific proteins and exhibit aggregation of these proteins. This is combated by the cellular protein...
2.
Brunt E, Boeree M
Eur J Neurol
. 2013 Nov;
2(2):127-32.
PMID: 24283613
We describe a parkinsonian patient who developed a slight asymptomatic pleural effusion during prolonged therapy with low dose bromocriptine (BCR) in addition to levodopa, following prior treatment with CQA 206-291....
3.
Rub U, Farrag K, Seidel K, Brunt E, Heinsen H, Burk K, et al.
Neuropathol Appl Neurobiol
. 2013 Feb;
39(6):634-43.
PMID: 23363055
Aims: Spinocerebellar ataxia type 2 (SCA2) belongs to the CAG repeat or polyglutamine diseases. Along with a large variety of motor, behavioural and neuropsychological symptoms the clinical picture of patients...
4.
Scherzed W, Brunt E, Heinsen H, de Vos R, Seidel K, Burk K, et al.
Cerebellum
. 2011 Dec;
11(3):749-60.
PMID: 22198871
The cerebellum is one of the well-known targets of the pathological processes underlying spinocerebellar ataxia type 2 (SCA2) and type 3 (SCA3). Despite its pivotal role for the clinical pictures...
5.
Seidel K, Vinet J, den Dunnen W, Brunt E, Meister M, Boncoraglio A, et al.
Neuropathol Appl Neurobiol
. 2011 Jun;
38(1):39-53.
PMID: 21696420
Aims: HSPB8 is a small heat shock protein that forms a complex with the co-chaperone BAG3. Overexpression of the HSPB8-BAG3 complex in cells stimulates autophagy and facilitates the clearance of...
6.
Zijlstra M, Rujano M, Van Waarde M, Vis E, Brunt E, Kampinga H
Eur J Neurosci
. 2010 Aug;
32(5):760-70.
PMID: 20726892
In polyglutamine disorders, the length of the expanded CAG repeat shows a strong inverse correlation with the age at disease onset, yet up to 50% of the variation in age...
7.
Sival D, du Marchie Sarvaas G, Brouwer O, Uges D, Verschuuren-Bemelmans C, Maurits N, et al.
Early Hum Dev
. 2009 Sep;
85(10):647-51.
PMID: 19775837
Introduction: In children with Friedreich's ataxia (FRDA children), clinical ataxia outcomes are hardly substantiated by underlying neurophysiological parameters. In young FRDA children, some reports (based upon International Cooperative Ataxia Rating...
8.
Verhagen M, Abdo W, Willemsen M, Hogervorst F, Smeets D, Hiel J, et al.
Neurology
. 2009 Jun;
73(6):430-7.
PMID: 19535770
Objective: To describe the phenotype of adult patients with variant and classic ataxia-telangiectasia (A-T), to raise the degree of clinical suspicion for the diagnosis variant A-T, and to assess a...
9.
Gierga K, Schelhaas H, Brunt E, Seidel K, Scherzed W, Egensperger R, et al.
Neuropathol Appl Neurobiol
. 2009 Feb;
35(5):515-27.
PMID: 19207264
Aims: Spinocerebellar ataxia type 6 (SCA6) is a late onset autosomal dominantly inherited ataxic disorder, which belongs to the group of CAG repeat, or polyglutamine, diseases. Although, it has long...
10.
Rub U, Heinsen H, Brunt E, Landwehrmeyer B, den Dunnen W, Gierga K, et al.
Neuropathol Appl Neurobiol
. 2009 Feb;
35(1):4-15.
PMID: 19187058
Recent progress in oculomotor research has enabled new insights into the functional neuroanatomy of the human premotor oculomotor brainstem network. In the present review, we provide an overview of its...