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

Tekijä Gallais Sérézal, I., Ferkal, S., Lerman, L., Mulé, S., Funalot, B., Wolkenstein, P.
Julkaisussa Orphanet J Rare Dis (2021)

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

Tekijä Funalot, B, Ranoux, D, Mas, J L, Garcia, C, Bonnefont, J P
Julkaistu 1996

FLNA genomic rearrangements cause periventricular nodular heterotopia

Tekijä 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.
Julkaistu 2012