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

Glucose 6-phosphate transport in fibroblast microsomes from glycogen storage disease type 1b patients: evidence for multiple glucose 6-phosphate transport systems.

Por Leuzzi, R, Fulceri, R, Marcolongo, P, Bánhegyi, G, Zammarchi, E, Stafford, K, Burchell, A, Benedetti, A
Publicado em 2001

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

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

Por D'Adamo, P, Fassone, L, Gedeon, A, Janssen, E A, Bione, S, Bolhuis, P A, Barth, P G, Wilson, M, Haan, E, Orstavik, K H, Patton, M A, Green, A J, Zammarchi, E, Donati, M A, Toniolo, D
Publicado em 1997