Bart P van de Warrenburg
Overview
Explore the profile of Bart P van de Warrenburg including associated specialties, affiliations and a list of published articles.
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Articles
109
Citations
2999
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Recent Articles
1.
Berger M, Garcia-Moreno H, Ferreira M, Hubener-Schmid J, Schaprian T, Wegner P, et al.
medRxiv
. 2025 Feb;
PMID: 39974031
Background: Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominantly inherited adult-onset disease. We aimed to describe longitudinal changes in clinical and biological findings and to identify predictors for clinical...
2.
Elter T, Sturm D, Santana M, Schaprian T, Raposo M, Melo A, et al.
J Neurol
. 2024 Dec;
272(1):54.
PMID: 39666145
Introduction: Knowledge about the distribution and frequency of the respective haplotypes on the wildtype and mutant allele is highly relevant in the context of future gene therapy clinical studies in...
3.
Boot E, Van Eeghen A, Bloem B, van de Warrenburg B, Cuypers M
Parkinsonism Relat Disord
. 2024 Sep;
128:107079.
PMID: 39276719
No abstract available.
4.
Multimodal, Longitudinal Profiling of SCA1 Identifies Predictors of Disease Severity and Progression
van Prooije T, Kapteijns K, van Asten J, IntHout J, Verbeek M, Scheenen T, et al.
Ann Neurol
. 2024 Aug;
96(4):774-787.
PMID: 39096063
Objectives: Spinocerebellar ataxia type 1 (SCA1) is a rare autosomal dominant neurodegenerative disease. Objective surrogate markers sensitive to detect changes in disease severity are needed to reduce sample sizes in...
5.
Scaravilli A, Gabusi I, Mari G, Battocchio M, Bosticardo S, Schiavi S, et al.
J Neurol
. 2024 Jun;
271(8):5468-5477.
PMID: 38880819
Background: Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Spastic Paraplegia Type 7 (SPG7) are paradigmatic spastic ataxias (SPAX) with suggested white matter (WM) involvement. Aim of this work was...
6.
Scaravilli A, Negroni D, Senatore C, Ugga L, Cosottini M, Ricca I, et al.
Mov Disord
. 2024 Jun;
39(8):1343-1351.
PMID: 38847051
Background: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) and hereditary spastic paraplegia type 7 (SPG7) represent the most common genotypes of spastic ataxia (SPAX). To date, their magnetic resonance imaging...
7.
Nonnekes J, van de Venis L, van de Warrenburg B, Lees A, Bloem B
Neurology
. 2024 May;
102(11):e209436.
PMID: 38718308
No abstract available.
8.
Potashman M, Rudell K, Pavisic I, Suminski N, Doma R, Heinrich M, et al.
Cerebellum
. 2024 May;
23(5):2012-2027.
PMID: 38713312
The functional Scale for the Assessment and Rating of Ataxia (f-SARA) assesses Gait, Stance, Sitting, and Speech. It was developed as a potentially clinically meaningful measure of spinocerebellar ataxia (SCA)...
9.
Raposo M, Hubener-Schmid J, Tagett R, Ferreira A, Melo A, Vasconcelos J, et al.
Neurobiol Dis
. 2024 Feb;
193:106456.
PMID: 38423193
Spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease (MJD) is a heritable proteinopathy disorder, whose causative gene, ATXN3, undergoes alternative splicing. Ataxin-3 protein isoforms differ in their toxicity, suggesting that certain ATXN3...
10.
van de Warrenburg B, Kamsteeg E
EBioMedicine
. 2024 Feb;
100:104994.
PMID: 38301484
No abstract available.