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Clarice Patrono

Schede primarie

Found 39 results
Filtri: Autore is Clarice Patrono
2000
Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation, Santorelli, F.M., Patrono Clarice, Fortini D., Tessa A., Comanducci G., Bertini E., Pierallini A., Amabile G.A., and Casali C. , Neurology, Volume 55, Number 5, p.702-705, (2000)
Letter to the editor, Tessa, A., Patrono Clarice, Santorelli F.M., Giannotti A., Digilio M.C., Pacifico C., Presuttari F., and Tieri L. , Journal of Medical Screening, Volume 7, Number 3, p.167, (2000)
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome, Patrono, Clarice, Rizzo C., Tessa A., Giannotti A., Borrelli P., Carrozzo R., Piemonte F., Bertini E., Dionisi-Vici C., and Santorelli F.M. , American Journal of Medical Genetics, Volume 91, Number 2, p.138-140, (2000)
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia., Giannotti, A., Tessa A., Patrono Clarice, Florio L.D., Velardo M., Dionisi-Vici C., Bertini E., and Santorelli F.M. , Human mutation, Volume 16, Number 3, p.277, (2000)
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiency, Santoro, L., Carrozzo R., Malandrini A., Piemonte F., Patrono Clarice, Villanova M., Tessa A., Palmeri S., Bertini E., and Santorelli F.M. , Neuromuscular Disorders, Volume 10, Number 6, p.450-453, (2000)
OXPHOS and mtDNA alterations in a family with spastic paraparesis, Santorelli, F.M., Piemonte F., Carrozzo R., Tessa A., Patrono Clarice, Tozzi G., and Bertini E. , Acta Neurologica Scandinavica, Volume 101, Number 4, p.255-258, (2000)