([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 en 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 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 2012