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Results: 1-11 |
Results: 11
Extracellular matrix globules in renal oncocytoma
Authors: Guarino, M Zuccoli, E Garda, E Cristofori, E Pallotti, F Nebuloni, M Giordano, F
Citation: M. Guarino et al., Extracellular matrix globules in renal oncocytoma, PATH RES PR, 197(4), 2001, pp. 245-252
The role of different biomarkers (DNA, PCNA, apoptosis and karyotype) in prognostic evaluation of superficial transitional cell bladder carcinoma
Authors: Lavezzi, AM Biondo, B Cazzullo, A Giordano, F Pallotti, F Turconi, P Matturri, L
Citation: Am. Lavezzi et al., The role of different biomarkers (DNA, PCNA, apoptosis and karyotype) in prognostic evaluation of superficial transitional cell bladder carcinoma, ANTICANC R, 21(2B), 2001, pp. 1279-1284
Renal pathological changes in Fabry disease
Authors: Sessa, A Meroni, M Battini, G Maglio, A Brambilla, PL Bertella, M Nebuloni, M Pallotti, F Giordano, F Bertagnolio, B Tosoni, A
Citation: A. Sessa et al., Renal pathological changes in Fabry disease, J INH MET D, 24, 2001, pp. 66-70
Isolation and subfractionation of mitochondria from animal cells and tissue culture lines
Authors: Pallotti, F Lenaz, G
Citation: F. Pallotti et G. Lenaz, Isolation and subfractionation of mitochondria from animal cells and tissue culture lines, METH CELL B, 65, 2001, pp. 1-35
Malaria placental infection with massive chronic intervillositis in a gravida 4 woman
Authors: Nebuloni, M Pallotti, F Polizzotti, G Pellegrinelli, A Tosi, D Giordano, F
Citation: M. Nebuloni et al., Malaria placental infection with massive chronic intervillositis in a gravida 4 woman, HUMAN PATH, 32(9), 2001, pp. 1022-1023
Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations
Authors: Sessa, A Battini, G Meroni, M Daidone, G Carnera, I Brambilla, PL Vigano, G Giordano, F Pallotti, F Tarelli, LT Calabresi, L Rolleri, M Bertolini, S
Citation: A. Sessa et al., Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations, NEPHRON, 88(3), 2001, pp. 268-272
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2
Authors: Sue, CM Karadimas, C Checcarelli, N Tanji, K Papadopoulou, LC Pallotti, F Guo, FL Shanske, S Hirano, M De Vivo, DC Van Coster, R Kaplan, P Bonilla, E DiMauro, S
Citation: Cm. Sue et al., Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2, ANN NEUROL, 47(5), 2000, pp. 589-595
Analysis of mtDNA deletions in muscle by in situ hybridization
Authors: Vu, TH Tanji, K Pallotti, F Golzi, V Hirano, M DiMauro, S Bonilla, E
Citation: Th. Vu et al., Analysis of mtDNA deletions in muscle by in situ hybridization, MUSCLE NERV, 23(1), 2000, pp. 80-85
Pathological relevance of epithelial and mesenchymal phenotype plasticity
Authors: Guarino, M Micheli, P Pallotti, F Giordano, F
Citation: M. Guarino et al., Pathological relevance of epithelial and mesenchymal phenotype plasticity, PATH RES PR, 195(6), 1999, pp. 379-389
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA
Authors: Andreu, AL Hanna, MG Reichmann, H Bruno, C Penn, AS Tanji, K Pallotti, F Iwata, S Bonilla, E Lach, B Morgan-Hughes, J DiMauro, S
Citation: Al. Andreu et al., Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA, N ENG J MED, 341(14), 1999, pp. 1037-1044
A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV
Authors: Bruno, C Martinuzzi, A Tang, YY Andreu, AL Pallotti, F Bonilla, E Shanske, S Fu, J Sue, CM Angelini, C DiMauro, S Manfredi, G
Citation: C. Bruno et al., A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV, AM J HU GEN, 65(3), 1999, pp. 611-620
Risultati: 1-11 |