RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.

Por Morrone, A, Pegoraro, E, Angelini, C, Zammarchi, E, Marconi, G, Hoffman, E P
Publicado em 1997

Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene

Por PORFIRIO, B., CHIARELLI, I., GRAZIANO, C., MANNONI, A., MORRONE, A., ZAMMARCHI, E., DE BERNABE, D. B.-V., DE CORDOBA, S. R.
Publicado em 2000

Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers

Por Morrone, A, Cavicchi, C, Bardelli, T, Antuzzi, D, Parini, R, Di, R, Feriozzi, S, Gabrielli, O, Barone, R, Pistone, G, Spisni, C, Ricci, R, Zammarchi, E
Publicado em 2003

FUNCTIONAL STUDIES OF NEW GLA GENE MUTATIONS LEADING TO CONFORMATIONAL FABRY DISEASE

Por Filoni, C., Caciotti, A., Carraresi, L., Cavicchi, C., Parini, R., Antuzzi, D., Zampetti, A., Feriozzi, S., Poisetti, P., Garman, S.C., Guerrini, R., Zammarchi, E., Donati, M.A., Morrone, A.
Publicado em 2009

Molecular Testing of 163 Patients with Morquio A (Mucopolysaccharidosis IVA) Identifies 39 Novel GALNS Mutations

Por Morrone, A, Tylee, K.L., Al-Sayed, M, Brusius-Facchin, A.C., Caciotti, A., Church, H.J., Coll, M.J., Davidson, K., Fietz, M.J., Gort, L., Hegde, M., Kubaski, F., Lacerda, L., Laranjeira, F., Leistner-Segal, S., Mooney, S., Pajares, S., Pollard, L., Riberio, I., Wang, R.Y., Miller, N.
Publicado em 2014