Alma Osmanovic
Overview
Explore the profile of Alma Osmanovic including associated specialties, affiliations and a list of published articles.
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44
Citations
723
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Recent Articles
11.
Freigang M, Steinacker P, Wurster C, Schreiber-Katz O, Osmanovic A, Petri S, et al.
Ann Clin Transl Neurol
. 2022 Aug;
9(9):1437-1448.
PMID: 35951535
Objective: Activated astroglia is involved in the pathophysiology of neurodegenerative diseases and has also been described in animal models of spinal muscular atrophy (SMA). Given the urgent need of biomarkers...
12.
Stolte B, Schreiber-Katz O, GuNTHER R, Wurster C, Petri S, Osmanovic A, et al.
Hum Gene Ther
. 2022 Aug;
33(17-18):968-976.
PMID: 35943879
5q-associated spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder that leads to progressive muscle atrophy and weakness. The disease is caused by a homozygous deletion or mutation in...
13.
Osmanovic A, Forster A, Widjaja M, Auber B, Das A, Christians A, et al.
J Neurol
. 2022 May;
269(9):4863-4871.
PMID: 35503374
Background: Recent evidence points toward a role of the small ubiquitin-like modifier (SUMO) system, including SUMO4, in protecting from stress insults and neurodegeneration, such as the progressive motor neuron disease...
14.
Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy
Binz C, Osmanovic A, Thomas N, Stolte B, Freigang M, Cordts I, et al.
Ann Clin Transl Neurol
. 2022 Feb;
9(3):351-362.
PMID: 35191616
Objective: Fatigue is a common and burdensome symptom of spinal muscular atrophy. Given its complex interactions, different dimensions of fatigue need to be investigated. The Multidimensional Fatigue Inventory is a...
15.
van Rheenen W, van der Spek R, Bakker M, van Vugt J, Hop P, Zwamborn R, et al.
Nat Genet
. 2022 Feb;
54(3):361.
PMID: 35102318
No abstract available.
16.
Osmanovic A, Gogol I, Martens H, Widjaja M, Muller K, Schreiber-Katz O, et al.
Genes (Basel)
. 2022 Jan;
13(1).
PMID: 35052424
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by progressive upper and lower motor neuron (LMN) loss. As ALS and other neurodegenerative diseases share genetic risk factors, we...
17.
van Rheenen W, van der Spek R, Bakker M, van Vugt J, Hop P, Zwamborn R, et al.
Nat Genet
. 2021 Dec;
53(12):1636-1648.
PMID: 34873335
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a lifetime risk of one in 350 people and an unmet need for disease-modifying therapies. We conducted a cross-ancestry genome-wide...
18.
Freigang M, Steinacker P, Wurster C, Schreiber-Katz O, Osmanovic A, Petri S, et al.
Orphanet J Rare Dis
. 2021 Jul;
16(1):330.
PMID: 34321067
Background: Studies regarding the impact of (neuro)inflammation and inflammatory response following repetitive, intrathecally administered antisense oligonucleotides (ASO) in 5q-associated spinal muscular atrophy (SMA) are sparse. Increased risk of hydrocephalus in...
19.
Schulze Westhoff M, Osmanovic A, Meissner C, Heck J, Mahmoudi N, Hendrich C, et al.
Clin Case Rep
. 2021 Jul;
9(7):e04547.
PMID: 34295499
We describe the case of a 59-year-old woman who exhibited psychotic symptoms, cognitive dysfunction, and restlessness. While the clinical picture and 18F-FDG PET/CT suggested the presence of a tauopathy, especially...
20.
Schischlevskij P, Cordts I, GuNTHER R, Stolte B, Zeller D, Schroter C, et al.
Brain Sci
. 2021 Jul;
11(6).
PMID: 34200087
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that causes progressive autonomy loss and need for care. This does not only affect patients themselves, but also the patients' informal...