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International Journal of Molecular Sciences|July 13, 2024
Characterisation of an Adult Zebrafish Model for SDHB-Associated Phaeochromocytomas and ParagangliomasJasmijn B Miltenburg, Marnix Gorissen, Inge van Outersterp, et al.
Neurology|January 23, 2020
Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophySaskia Lassche, Nicol C Voermans, Robbert van der Pijl, et al.
Acta Neuropathologica Communications|November 22, 2019
Mapping actionable pathways and mutations in brain tumours using targeted RNA next generation sequencingKrissie Lenting, Corina N A M van den Heuvel, Anne van Ewijk, et al.
Carcinogenesis|March 15, 2013
A promoter polymorphism in human interleukin-32 modulates its expression and influences the risk and the outcome of epithelial cell-derived thyroid carcinomaTheo S Plantinga, Irene Costantini, Bas Heinhuis, et al.
Frontiers in Endocrinology|April 3, 2026
Long-term culture of patient-derived pheochromocytoma organoidsMarit F van den Berg, Elpetra P M Timmermans-Sprang, Jan Zethof, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 18, 2015
Semiquantitative 123I-Metaiodobenzylguanidine Scintigraphy to Distinguish Pheochromocytoma and Paraganglioma from Physiologic Adrenal Uptake and Its Correlation with Genotype-Dependent Expression of Catecholamine TransportersAnouk van Berkel, Jyotsna U Rao, Jacques W M Lenders, et al.
Skeletal Muscle|March 7, 2023
The double homeodomain protein DUX4c is associated with regenerating muscle fibers and RNA-binding proteinsClothilde Claus, Moriya Slavin, Eugénie Ansseau, et al.
Clinical Genetics|August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the NetherlandsStacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Human Mutation|April 2, 2019
Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathiesChristoph Bachmann, Faiza Noreen, Nicol C Voermans, et al.
European Journal of Endocrinology|October 7, 2017
Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumorLuis G Pérez-Rivas, Marily Theodoropoulou, Troy H Puar, et al.
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