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Elisabeth M W Eekhoff

Explore the profile of Elisabeth M W Eekhoff including associated specialties, affiliations and a list of published articles. Areas
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Articles 57
Citations 816
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Recent Articles
1.
de Ruiter R, Zwama J, Raijmakers P, Yaqub M, Burchell G, Boellaard R, et al.
Ann Nucl Med . 2024 Dec; 39(2):98-149. PMID: 39729191
Purpose: [F]NaF PET has become an increasingly important tool in clinical practice toward understanding and evaluating diseases and conditions in which bone metabolism is disrupted. Full kinetic analysis using nonlinear...
2.
Zelis M, Simonis A, van Dam R, Boomsma D, van Lee L, Kramer M, et al.
Nutrients . 2024 Oct; 16(20). PMID: 39458507
Aims: Various dietary risk factors for type 2 diabetes have been identified. A short assessment of dietary patterns related to the risk for type 2 diabetes mellitus may be relevant...
3.
Zwama J, Rosenberg N, Verheij V, Raijmakers P, Yaqub M, Botman E, et al.
Biomolecules . 2024 Oct; 14(10). PMID: 39456213
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic bone disorder characterized by episodic flare-ups in connective tissue, which are frequently followed by the formation of heterotopic ossification. The absence of...
4.
de Ruiter R, Treurniet S, Bravenboer N, Busse B, Hendrickx J, Jansen J, et al.
JBMR Plus . 2024 Sep; 8(10):ziae115. PMID: 39347481
Eagle syndrome is a bone disease where elongation of the styloid process leads to throat and neck pain, and in severe cases neurovascular symptoms such as syncope and neuralgia. The...
5.
Ventura L, Verdonk S, Zhytnik L, Ridwan-Pramana A, Gilijamse M, Schreuder W, et al.
Calcif Tissue Int . 2024 Sep; 115(5):461-479. PMID: 39294450
Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by fragile bones and skeletal deformities. Individuals with OI may have dental abnormalities such as dentinogenesis imperfecta (DI) type I, malocclusions,...
6.
Zhong W, Neugebauer J, Pathak J, Li X, Pals G, Zillikens M, et al.
Cells . 2024 Sep; 13(17. PMID: 39273077
Plastin-3 (PLS3) encodes T-plastin, an actin-bundling protein mediating the formation of actin filaments by which numerous cellular processes are regulated. Loss-of-function genetic defects in PLS3 are reported to cause X-linked...
7.
Verdonk S, Storoni S, Zhytnik L, Micha D, van den Aardweg J, Kamp O, et al.
Pediatr Dev Pathol . 2024 Aug; 28(1):24-30. PMID: 39189102
Introduction: Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility. While skeletal manifestations are well documented, few studies have explored the effect of OI on the fetal...
8.
Claeys L, Zhytnik L, Ventura L, Wisse L, Eekhoff E, Pals G, et al.
Int J Mol Sci . 2024 Mar; 25(6). PMID: 38542391
(1) Mesenchymal stem cells (MSCs) are a valuable cell model to study the bone pathology of Osteogenesis Imperfecta (OI), a rare genetic collagen-related disorder characterized by bone fragility and skeletal...
9.
Verdonk S, Storoni S, Micha D, van den Aardweg J, Versacci P, Celli L, et al.
Calcif Tissue Int . 2024 Jan; 114(3):210-221. PMID: 38243143
Osteogenesis imperfecta (OI) is a rare genetic disorder caused by abnormal collagen type I production. While OI is primarily characterized by bone fragility and deformities, patients also have extraskeletal manifestations,...
10.
Storoni S, Verdonk S, Micha D, Jak P, Bugiani M, Eekhoff E, et al.
Front Med (Lausanne) . 2024 Jan; 10:1301873. PMID: 38179272
Introduction: Respiratory insufficiency is a leading cause of death in individuals with osteogenesis imperfecta (OI). However, evaluating pulmonary function in OI presents challenges. Commonly used pulmonary function tests such as...