Benno Kusters
Overview
Explore the profile of Benno Kusters including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
121
Citations
2377
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Malaichamy S, Idoux R, Polavarapu K, Sikic K, Holla E, Thompson R, et al.
Brain
. 2025 Feb;
PMID: 39970126
Rhabdomyolysis is an acute failure of cellular homeostasis resulting in muscle breakdown, triggered by trauma, infection, drugs, or strenuous exercise. Recurrent rhabdomyolysis is often associated with genetic and metabolic defects...
2.
Saris C, van Engelen B, Janssen M, Kusters B, Rodenburg R, Sluijs D, et al.
Nat Commun
. 2025 Feb;
16(1):1724.
PMID: 39966388
No abstract available.
3.
van Kleef E, Bouman K, Molenaar J, Kusters B, Groothuis J, Olive M, et al.
Neurol Genet
. 2024 Dec;
10(6):e200214.
PMID: 39651462
Background And Objectives: Nemaline myopathy type 6 (NEM6) is the most prevalent type of nemaline myopathy in the Netherlands. Because a detailed clinical characterization is not available yet, we here...
4.
Nagy S, Pagnamenta A, Cali E, Braakman H, Wijntjes J, Kusters B, et al.
Brain Commun
. 2024 Nov;
6(6):fcae377.
PMID: 39502942
A newly identified subtype of hereditary axonal motor neuropathy, characterized by early proximal limb involvement, has been discovered in a cohort of 34 individuals with biallelic variants in von Willebrand...
5.
Gelpi E, Reinecke R, Gaig C, Iranzo A, Sabater L, Molina-Porcel L, et al.
Acta Neuropathol
. 2024 Oct;
148(1):53.
PMID: 39400557
Anti-IgLON5 disease is a unique condition that bridges autoimmunity and neurodegeneration. Since its initial description 10 years ago, an increasing number of autopsies has led to the observation of a...
6.
Brouwers K, van Geel S, van Midden D, Kruit A, Kusters B, Hummelink S, et al.
J Clin Med
. 2024 Sep;
13(17).
PMID: 39274379
: Machine perfusion (MP) offers extended preservation of vascularized complex allografts (VCA), but the diagnostic value of histology using hematoxylin and eosin (H&E) in detecting ischemia-reperfusion injury (IRI) in muscle...
7.
van Kleef E, Bouman K, Molenaar J, de Winter J, Duijkers F, Eftimov F, et al.
J Neuromuscul Dis
. 2024 Sep;
11(6):1300-1307.
PMID: 39240645
Background: Nemaline myopathy type 6 (NEM6) or KBTBD13-related congenital myopathy is the most prevalent type of nemaline myopathy in the Netherlands and is characterised by mild childhood-onset axial, proximal and...
8.
Jansen N, Dittrich A, Backes M, Kusters B, Klein W, Hundscheid T
BMC Pediatr
. 2024 Sep;
24(1):564.
PMID: 39237896
Two cases of neonatal splenic hemorrhage with acute cardiorespiratory failure are described in this report. The first case involves a full-term neonate who was found unresponsive without any witnesses and...
9.
van Kleef E, van de Camp S, Groothuis J, Erasmus C, Gaytant M, Vosse B, et al.
Neuromuscul Disord
. 2024 Aug;
43:29-38.
PMID: 39180840
Nemaline myopathy (NM) is a congenital myopathy with generalised muscle weakness, most pronounced in neck flexor, bulbar and respiratory muscles. The aim of this cross-sectional study was to assess the...
10.
Sole-Guardia G, Luijten M, Janssen E, Visch R, Geenen B, Kusters B, et al.
Brain Pathol
. 2024 Aug;
35(2):e13301.
PMID: 39175459
The major vascular cause of dementia is cerebral small vessel disease (SVD). Its diagnosis relies on imaging hallmarks, such as white matter hyperintensities (WMH). WMH present a heterogenous pathology, including...