María
Currás Freixes
Forscherin bis um 2022
Erasmus University Medical Center
Róterdam, HolandaPublikationen in Zusammenarbeit mit Forschern von Erasmus University Medical Center (4)
2018
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Role of MDH2 pathogenic variant in pheochromocytoma and paraganglioma patients
Genetics in Medicine, Vol. 20, Núm. 12, pp. 1652-1662
2017
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PheoSeq: A Targeted Next-Generation Sequencing Assay for Pheochromocytoma and Paraganglioma Diagnostics
Journal of Molecular Diagnostics, Vol. 19, Núm. 4, pp. 575-588
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The mTORC1 Complex Is Significantly Overactivated in SDHX -Mutated Paragangliomas
Neuroendocrinology, Vol. 105, Núm. 4, pp. 384-393
2015
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Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients
Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656