Jo M. Vanoevelen
Maastricht, LI 6229HX, Netherlands
Last Updated: 09/26/2026
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Found 20 publications
Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A: sentinel event for evolving dilated cardiomyopathy-a case report.
Journal: European heart journal. Case reports
Published: November 11, 2022
Novel mRNA therapy restores GALT protein and enzyme activity in a zebrafish model of classic galactosemia.
Journal: Journal of inherited metabolic disease
Published: February 10, 2022
DTYMK is essential for genome integrity and neuronal survival.
Journal: Acta neuropathologica
Published: June 08, 2021
Dopamine-neurotransmission and nociception in zebrafish: An anti-nociceptive role of dopamine receptor drd2a.
Journal: European journal of pharmacology
Published: January 26, 2021
Multiview deconvolution approximation multiphoton microscopy of tissues and zebrafish larvae.
Journal: Scientific reports
Published: December 17, 2020
Nucleotide sugar profiles throughout development in wildtype and galt knockout zebrafish.
Journal: Journal of inherited metabolic disease
Published: April 09, 2020
Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models.
Journal: Journal of inherited metabolic disease
Published: August 16, 2019
An N-terminal Ca2+-binding motif regulates the secretory pathway Ca2+/Mn2+-transport ATPase SPCA1.
Journal: The Journal of biological chemistry
Published: October 12, 2018
Δ9-tetrahydrocannabivarin impairs epithelial calcium transport through inhibition of TRPV5 and TRPV6.
Journal: Pharmacological research
Published: July 31, 2018
Yield of peripheral sodium channels gene screening in pure small fibre neuropathy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: June 18, 2018
Expression of pathogenic SCN9A mutations in the zebrafish: A model to study small-fiber neuropathy.
Journal: Experimental neurology
Published: April 18, 2018
Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause.
Journal: Frontiers in genetics
Published: April 03, 2018
Last Updated: 09/26/2026