Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene.

door Gellera, C., Meoni, C., Castellotti, B., Zappacosta, B., Girotti, F., Taroni, F., DiDonato, S.
Gepubliceerd in 1996

Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case report

door Zerkaoui, M., Ratbi, I., Castellotti, B., Gellera, C., Lyahyai, J., Kriouile, Y., Sefiani, A.
Gepubliceerd in BMC Pediatr (2015)

P-14 Multiple acyl-coa dehydrogenase deficiency: a possibly treatable condition

door Todeschini, A., Cotelli, M.S., Vielmi, V., Rimoldi, M., Gregorelli, V., Rizzetto, M., Castellotti, B., Padovani, A., Filosto, M.
Gepubliceerd in 2011