([18F])FDG Positron emission tomography with whole body magnetic resonance imaging (([18F])FDG-PET/MRI) as a diagnosis tool in Schwannomatosis

Por Gallais Sérézal, I., Ferkal, S., Lerman, L., Mulé, S., Funalot, B., Wolkenstein, P.
Publicado no Orphanet J Rare Dis (2021)

Brainstem involvement in Leber's hereditary optic neuropathy: association with the 14,484 mitochondrial DNA mutation.

Por Funalot, B, Ranoux, D, Mas, J L, Garcia, C, Bonnefont, J P
Publicado em 1996

FLNA genomic rearrangements cause periventricular nodular heterotopia

Por Clapham, K.R., Yu, T.W., Ganesh, V.S., Barry, B., Chan, Y., Mei, D., Parrini, E., Funalot, B., Dupuis, L., Nezarati, M.M., du Souich, C., van Karnebeek, C., Guerrini, R., Walsh, C.A.
Publicado em 2012