Wolfgang N Loscher
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Explore the profile of Wolfgang N Loscher including associated specialties, affiliations and a list of published articles.
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73
Citations
982
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Recent Articles
1.
Adreana Kleinveld V, Emmelheinz M, Egle D, Ritter M, Loscher W, Marth C, et al.
Diagnostics (Basel)
. 2025 Jan;
14(24.
PMID: 39767220
Neurotoxic effects causing peripheral nerve damage have been reported for several chemotherapy agents. There is no established and standardized method to assess the presence of chemotherapy-induced peripheral neuropathy (CIPN). We...
2.
Adreana Kleinveld V, Wanschitz J, Loscher W, Hotter A, Cornelia Horlings C
Immunotherapy
. 2024 Jul;
16(9):597-601.
PMID: 39052281
Immune checkpoint inhibitors (ICIs) have significantly improved the clinical outcome in multiple types of advanced or metastatic malignancies and are prescribed increasingly. However, immune-related adverse events (irAEs) occur frequently. Here,...
3.
Meyer T, Dreger M, Grehl T, Weyen U, Kettemann D, Weydt P, et al.
Eur J Neurol
. 2024 Jun;
31(9):e16379.
PMID: 38859579
Objective: To assess the performance of serum neurofilament light chain (sNfL) in clinical phenotypes of amyotrophic lateral sclerosis (ALS). Methods: In 2949 ALS patients at 16 ALS centers in Germany...
4.
Topf A, Cox D, Zaharieva I, Di Leo V, Sarparanta J, Jonson P, et al.
Nat Genet
. 2024 Mar;
56(3):395-407.
PMID: 38429495
In digenic inheritance, pathogenic variants in two genes must be inherited together to cause disease. Only very few examples of digenic inheritance have been described in the neuromuscular disease field....
5.
Kleinveld V, Keritam O, Horlings C, Cetin H, Wanschitz J, Hotter A, et al.
Muscle Nerve
. 2024 Feb;
69(4):422-427.
PMID: 38334356
Introduction/aims: The clinical presentation of multifocal motor neuropathy (MMN) may mimic early amyotrophic lateral sclerosis (ALS) with predominant lower motor neuron (LMN) involvement, posing a diagnostic challenge. Both diseases have...
6.
Kleinveld V, Platzgummer S, Wanschitz J, Horlings C, Loscher W
Brain Sci
. 2023 May;
13(4).
PMID: 37190588
(1) Background: This study aims to assess the diagnostic accuracy of parameters based on a combination of transcranial magnetic stimulation (TMS) and electrical stimulation (ES) in the differentiation between idiopathic...
7.
Bergmann M, Wanschitz J, Stefani A, Heidbreder A, Brandauer E, Cesari M, et al.
Sleep Med
. 2023 Apr;
106:84-89.
PMID: 37075530
Background: Excessive fragmentary myoclonus (EFM) is an incidental finding in video-polysomnography (VPSG) and listed among "Sleep Related Movement Disorders - Isolated symptoms and normal variants" in the ICSD-3. We aimed...
8.
Krenn M, Sener M, Rath J, Zulehner G, Keritam O, Wagner M, et al.
J Neurol
. 2022 Oct;
270(2):909-916.
PMID: 36308527
Background: Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders caused by genetic defects resulting in impaired neuromuscular transmission. Although effective treatments are available, CMS is probably underdiagnosed, and...
9.
Gasser L, Lener S, Hartmann S, Loscher W, Thome C, Hofer A
Neurosurg Rev
. 2022 May;
45(4):2941-2949.
PMID: 35608709
The importance of the type of pain medication in spinal disease is an ongoing matter of debate. Recent guidelines recommend acetaminophen and NSAIDs as first-line medication for lumbar disc herniation....
10.
Enax-Krumova E, Dahlhaus I, Gorlach J, Claeys K, Montagnese F, Schneider L, et al.
Orphanet J Rare Dis
. 2022 Apr;
17(1):177.
PMID: 35477515
Background: Pain occurs in the majority of patients with late onset Pompe disease (LOPD) and is associated with a reduced quality of life. The aim of this study was to...