Andreas Traschutz
Overview
Explore the profile of Andreas Traschutz including associated specialties, affiliations and a list of published articles.
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Articles
51
Citations
705
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Recent Articles
1.
Beichert L, Seemann J, Kessler C, Traschutz A, Muller D, Dillmann-Jehn K, et al.
Neurology
. 2024 Dec;
103(12):e209887.
PMID: 39621946
Background And Objectives: With targeted treatment trials on the horizon, identification of sensitive and valid outcome measures becomes a priority for >100 spastic ataxias. While digital-motor measures, assessed using wearable...
2.
Hamdan A, Hendrickx N, Hooker A, Chen X, Comets E, Traschutz A, et al.
Clin Pharmacol Ther
. 2024 Oct;
116(6):1593-1605.
PMID: 39403821
Degenerative cerebellar ataxias comprise a heterogeneous group of rare and ultra-rare genetic diseases. While disease-modifying treatments are now on the horizon for many ataxias, robust trial designs and analysis methods...
3.
Tunca C, Islek Camadan E, Smolina N, Palvadeau R, Oztop Cakmak O, Vural A, et al.
Mov Disord
. 2024 Sep;
39(12):2291-2297.
PMID: 39314081
Background: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a common recessive ataxia that is still underdiagnosed worldwide. An easily accessible diagnostic biomarker might help to diagnostically confirm patients presenting...
4.
Pellerin D, Seemann J, Traschutz A, Brais B, Ilg W, Synofzik M
Mov Disord
. 2024 Jul;
39(10):1892-1894.
PMID: 38949032
No abstract available.
5.
Beichert L, Ilg W, Kessler C, Traschutz A, Reich S, Santorelli F, et al.
Mov Disord
. 2024 Jun;
39(9):1544-1555.
PMID: 38847438
Background: With treatment trials on the horizon, this study aimed to identify candidate digital-motor gait outcomes for autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), capturable by wearable sensors with multicenter...
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.
Hendrickx N, Mentre F, Traschutz A, Gagnon C, Schule R, Synofzik M, et al.
AAPS J
. 2024 May;
26(4):62.
PMID: 38789847
No abstract available.
8.
Hamdan A, Hooker A, Chen X, Traschutz A, Schule R, Synofzik M, et al.
CPT Pharmacometrics Syst Pharmacol
. 2024 May;
13(8):1327-1340.
PMID: 38769902
The Scale for the Assessment and Rating of Ataxia (SARA) is widely used for assessing the severity and progression of genetic cerebellar ataxias. SARA is now considered a primary end...
9.
Hendrickx N, Mentre F, Traschutz A, Gagnon C, Schule R, Synofzik M, et al.
AAPS J
. 2024 Apr;
26(3):57.
PMID: 38689016
The aim of this study was to develop a model to predict individual subject disease trajectories including parameter uncertainty and accounting for missing data in rare neurological diseases, showcased by...
10.
Hermle D, Schubert R, Barallon P, Ilg W, Schule R, Reilmann R, et al.
Ann Clin Transl Neurol
. 2024 Apr;
11(5):1097-1109.
PMID: 38590028
Objective: Voluntary upper limb movements are an ecologically important yet insufficiently explored digital-motor outcome domain for trials in degenerative ataxia. We extended and validated the trial-ready quantitative motor assessment battery...