Authors:
Pequignot, MO
Dey, R
Zeviani, M
Tiranti, V
Godinot, C
Poyau, A
Sue, C
Di Mauro, S
Abitbol, M
Marsac, C
Citation: Mo. Pequignot et al., Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome c oxidase deficiency, HUM MUTAT, 17(5), 2001, pp. 374-381
Authors:
Di Giovanni, S
Mirabella, M
Spinazzola, A
Crociani, P
Silvestri, G
Broccolini, A
Tonali, P
Di Mauro, S
Servidei, S
Citation: S. Di Giovanni et al., Coenzyme Q(10) reverses pathological phenotype and reduces apoptosis in familial CoQ(10) deficiency, NEUROLOGY, 57(3), 2001, pp. 515-518
Authors:
Di Mauro, S
Scalia, G
Leotta, C
Giuffrida, F
Di Stefano, A
Malaguarnera, M
Citation: S. Di Mauro et al., The care of elderly, terminally ill oncological patients in caregiving sanitary residences, ARCH GER G, 31(1), 2000, pp. 85-94
Authors:
White, SL
Shanske, S
Biros, I
Warwick, L
Dahl, HM
Thorburn, DR
Di Mauro, S
Citation: Sl. White et al., Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA, PRENAT DIAG, 19(12), 1999, pp. 1165-1168
Authors:
Torrisi, G
Leotta, C
Scalia, G
Spallina, G
Distefano, A
Di Mauro, S
Citation: G. Torrisi et al., Echocardiographic studies on elderly patients with white coat hypertensionto evaluate cardiac organ damages, ARCH GER G, 29(2), 1999, pp. 127-138