|
|
Repositório Científico do Instituto Nacional de Saúde >
Browsing by Author Ferreira, M.
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | | Jun-2012 | "Double trouble” or digenic disorder in Complex I deficiency | Almeida, L.S.; Ferreira, M.; Nogueira, C.; Furtado, F.; Evangelista, T.; Santorelli, F.M.; Vilarinho, L. |
| 2011 | Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1 | Ferreira, M.; Torraco, A.; Rizza, T.; Fattori, F.; Meschini, M.C.; Castana, C.; Go, N.E.; Nargang, F.E.; Duarte, M.; Piemonte, F.; Dionisi-Vici, C.; Videira, A.; Vilarinho, L.; Santorelli, F.M.; Carrozzo, R.; Bertini, E. |
| 2011 | Relative frequency of known causes of multiple mtDNA deletions: two novel POLG mutations | Ferreira, M.; Evangelista, T.; Almeida, L.S.; Martins, J.; Macario, M.C.; Martins, E.; Moleirinho, A.; Azevedo, L.; Vilarinho, L.; Santorelli, F.M. |
Showing results 1 to 3 of 3
|
