The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia

Por Meyer, T., Munch, C., Volkel, H., Booms, P., Ludolph, A.
Publicado em 1998

Small-sized granules of biphasic bone substitutes support fast implant bed vascularization

Por Barbeck, M, Dard, M, Kokkinopoulou, M, Markl, J, Booms, P, Sader, RA, Kirkpatrick, CJ, Ghanaati, S
Publicado no Biomatter (2015)

The molecular genetics of Marfan syndrome and related disorders

Por Robinson, P N, Arteaga‐Solis, E, Baldock, C, Collod‐Béroud, G, Booms, P, De Paepe, A, Dietz, H C, Guo, G, Handford, P A, Judge, D P, Kielty, C M, Loeys, B, Milewicz, D M, Ney, A, Ramirez, F, Reinhardt, D P, Tiedemann, K, Whiteman, P, Godfrey, M
Publicado em 2006