Veerle Goosens
Overview
Explore the profile of Veerle Goosens including associated specialties, affiliations and a list of published articles.
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Articles
10
Citations
66
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0
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Recent Articles
1.
Claeys K, Savarese M, Jonson P, Goosens V, Topf A, Vihola A, et al.
Neurol Genet
. 2024 Oct;
10(5):e200185.
PMID: 39376211
Background: Titin truncating variants (TTNtvs) have been repeatedly reported as causative of recessive but not dominant skeletal muscle disorders. Objective: To determine whether a single heterozygous nonsense variant in can...
2.
De Wel B, Iterbeke L, Huysmans L, Peeters R, Goosens V, Dubuisson N, et al.
Eur J Neurol
. 2024 Mar;
31(7):e16282.
PMID: 38504654
Background And Purpose: Because Becker muscular dystrophy (BMD) is a heterogeneous disease and only few studies have evaluated adult patients, it is currently still unclear which outcome measures should be...
3.
De Wel B, Huysmans L, Depuydt C, Goosens V, Peeters R, Santos F, et al.
J Cachexia Sarcopenia Muscle
. 2023 Apr;
14(3):1468-1481.
PMID: 37078404
Background: Despite the widespread use of proton density fat fraction (PDFF) measurements with magnetic resonance imaging (MRI) to track disease progression in muscle disorders, it is still unclear how these...
4.
Hustings N, Goosens V, Vanderschueren G
J Belg Soc Radiol
. 2022 May;
106(1):23.
PMID: 35581981
Extramedullary acute myeloid leukemia tumor belongs to the differential diagnosis when a tumor develops in a patient with a history of leukemia, and magnetic resonance imaging is of diagnostic value...
5.
De Wel B, Huysmans L, Peeters R, Goosens V, Ghysels S, Byloos K, et al.
Neurology
. 2022 May;
99(6):e638-e649.
PMID: 35577579
Background And Objectives: Limb-girdle muscular dystrophy autosomal recessive type 12 (LGMDR12) is a rare hereditary muscular dystrophy for which outcome measures are currently lacking. We evaluated quantitative MRI and clinical...
6.
Depuydt C, Goosens V, Janky R, DHondt A, De Bleecker J, Noppe N, et al.
Cells
. 2022 May;
11(9).
PMID: 35563815
Limb-girdle muscular dystrophy R12 (LGMD-R12) is caused by two mutations in anoctamin-5 (). Our aim was to identify genes and pathways that underlie LGMD-R12 and explain differences in the molecular...
7.
De Wel B, Goosens V, Sobota A, Van Camp E, Geukens E, Van Kerschaver G, et al.
J Neurol
. 2020 Sep;
268(3):923-935.
PMID: 32935160
Background: Nusinersen recently became available as the first treatment for Spinal Muscular Atrophy (SMA) and data on its effectiveness and safety in adult SMA patients are still scarce. Methods: We...
8.
Claeys T, Goosens V, Race V, Theys T, Thal D, Depuydt C, et al.
Neuromuscul Disord
. 2020 Sep;
30(9):709-718.
PMID: 32893083
Heterozygous mutations in the stromal interaction molecule-1-gene (STIM1) cause a clinical phenotype varying from tubular aggregate myopathy with single or multiple signs of Stormorken syndrome to the full Stormorken phenotype....
9.
TSeyen S, Bertrand P, Goosens V, Stas M, Verhamme P, Maleux G
Vasa
. 2013 Feb;
42(1):72-6.
PMID: 23385229
No abstract available.
10.
Breysem L, Goosens V, Vander Poorten V, Vanhole C, Proesmans M, Smet M
Pediatr Radiol
. 2009 May;
39(8):828-31.
PMID: 19458946
Background: Vallecular cysts are an unusual cause of congenital stridor. Objective: To describe the imaging findings in five patients, with emphasis on the usefulness of sonographic studies. Materials And Methods:...