Christian Sass
Overview
Explore the profile of Christian Sass including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
167
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0
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Recent Articles
1.
Medzech S, Sass C, Bohlen S, Lange H, Koch R, Schubert R, et al.
J Huntingtons Dis
. 2019 Aug;
8(4):483-492.
PMID: 31450507
Background: Assessment of motor symptoms in Huntington's disease (HD) is based on the Unified-HD-Rating-Scale-Total-Motor-Score (UHDRS-TMS). Its categorical and rater-dependent nature reduces the ability to detect subtle changes and often placebo...
2.
Reilmann R, Schubert R, Bohlen S, Sass C
Mov Disord
. 2018 Sep;
33(8):1370-1371.
PMID: 30230629
No abstract available.
3.
Hoffmann S, Siedler J, Brandt A, Piper S, Kohler S, Sass C, et al.
BMC Neurol
. 2015 Dec;
15:265.
PMID: 26701600
Background: Muscular weakness in myasthenia gravis (MG) is commonly assessed using Quantitative Myasthenia Gravis Score (QMG). More objective and quantitative measures may complement the use of clinical scales and might...
4.
Maetzler W, Ellerbrock M, Heger T, Sass C, Berg D, Reilmann R
PLoS One
. 2015 Apr;
10(4):e0123914.
PMID: 25902182
Motor symptoms in Parkinson's disease (PD) are usually assessed with semi-quantitative tests such as the Unified PD Rating Scale (UPDRS) which are limited by subjectivity, categorical design, and low sensitivity....
5.
Schaeffer E, Maetzler W, Liepelt-Scarfone I, Sass C, Reilmann R, Berg D
J Neural Transm (Vienna)
. 2015 Feb;
122(9):1271-8.
PMID: 25712401
Although Levodopa-induced dyskinesias (LID) are one of the most compromising complications of dopaminergic treatment in Parkinson's disease (PD), there is no widely accepted assessment tool available that evaluates LID quantitatively....
6.
Werner C, Dogan I, Sass C, Mirzazade S, Schiefer J, Jon Shah N, et al.
Hum Brain Mapp
. 2013 Aug;
35(6):2582-93.
PMID: 23982979
Huntington's disease (HD) is an autosomal dominantly inherited neurodegenerative disorder characterized by motor, cognitive, and psychiatric symptoms. Using resting-state fMRI (rs-fMRI) we investigated the functional integrity of resting-state networks (RSN)...
7.
Dogan I, Sass C, Mirzazade S, Kleiman A, Werner C, Pohl A, et al.
Soc Cogn Affect Neurosci
. 2013 Mar;
9(5):671-80.
PMID: 23482620
The complex phenotype of Huntington's disease (HD) encompasses motor, psychiatric and cognitive dysfunctions, including early impairments in emotion recognition. In this first functional magnetic resonance imaging study, we investigated emotion-processing...
8.
Sass C, Kosinski C, Schmidt P, Mull M, Schulz J, Schiefer J
Neurocrit Care
. 2012 Oct;
19(1):116-8.
PMID: 23055090
Background: Spontaneous intracranial hypotension (SIH) is a neurologic condition with the prototypical symptom of orthostatic headache. We report a dramatic case of SIH with life-threatening bilateral hygroma and uncal herniation....
9.
Reetz K, Romanzetti S, Dogan I, Sass C, Werner C, Schiefer J, et al.
Neuroimage
. 2012 Jul;
63(1):517-24.
PMID: 22796981
The neuropathological hallmark of the autosomal dominantly inherited, neurodegenerative disorder Huntington's disease is progressive striatal loss starting several years prior to symptom manifestation. Magnetic resonance (MR) imaging has been widely...
10.
Huang B, Schiefer J, Sass C, Kosinski C, Kochanek S
J Gene Med
. 2007 Dec;
10(3):269-79.
PMID: 18067195
Background: Huntington's disease (HD) is an inherited autosomal dominant neurodegenerative disease caused by the expansion of a CAG trinucleotide repeat in exon 1 of the huntingtin (htt) gene. Vector-mediated delivery...