Electrical impedance to easily discover undeclared freeze-thaw cycles in slaughtered bovine meat

Por Dell’Osa A. H., Battacone G., Pulina G., Fois A., Tocco F., Loviselli A., Concu A., Velluzzi F.
Publicado em 2021-03-01

Cerebral glucose metabolism in neurofibromatosis type 1 assessed with [18F]-2-fluoro-2-deoxy-D-glucose and PET.

Por Balestri, P, Lucignani, G, Fois, A, Magliani, L, Calistri, L, Grana, C, Di Bartolo, R M, Perani, D, Fazio, F
Publicado em 1994

Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruva...

Por Chun, K, MacKay, N, Petrova-Benedict, R, Federico, A, Fois, A, Cole, D E, Robertson, E, Robinson, B H
Publicado em 1995

The Molecular Basis of Canavan (Aspartoacylase Deficiency) Disease in European Non-Jewish Patients

Por Shaag, A., Anikster, Y., Christensen, E., Glustein, J. Z., Fois, A., Michelakakis, H., Nigro, F., Pronicka, E., Ribes, A., Zabot, M. T., Elpeleg, O. N.
Publicado em 1995

Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.

Por Carrozzo, R, Rossi, E, Christian, S L, Kittikamron, K, Livieri, C, Corrias, A, Pucci, L, Fois, A, Simi, P, Bosio, L, Beccaria, L, Zuffardi, O, Ledbetter, D H
Publicado em 1997

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

Por Eussen, B., Bartalini, G., Bakker, L., Balestri, P., Di, L, Van Hemel, J. O, Dauwerse, H., van den Ouweland, A. M W, Ris-Stalpers, C., Verhoef, S., Halley, D., Fois, A.
Publicado em 2000

High rate of mosaicism in tuberous sclerosis complex.

Por Verhoef, S, Bakker, L, Tempelaars, A M, Hesseling-Janssen, A L, Mazurczak, T, Jozwiak, S, Fois, A, Bartalini, G, Zonnenberg, B A, van Essen, A J, Lindhout, D, Halley, D J, van den Ouweland, A M
Publicado em 1999