Martin Lammens
0000-0002-3881-6692
4 papers found
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Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants
Feasibility and safety of synchrotron-based X-ray phase contrast imaging as a technique complementary to histopathology analysis
Neuropathological Changes in Nakalanga Syndrome—A Case Report
Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections
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