Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity von STEFANINI, M, LAGOMARSINI, P, ARLETT, C. F, MARINONI, S, BORRONE, C, CROVATO, F, TREVISAN, G, CORDONE, G, NUZZO, F

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Response of mammalian ADP-ribosyl transferase to lymphocyte stimulation, mutagen treatment and cell cycling von Scovassi, A.I., Stefanini, M., Lagomarsini, P., Izzo, R., Bertazzoni, U.

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Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defects von Stefanini, M., Scappaticci, S., Lagomarsini, P., Borroni, G., Berardesca, E., Nuzzo, F.

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Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosum von Nuzzo, F, Zei, G, Stefanini, M, Colognola, R, Santachiara, A S, Lagomarsini, P, Marinoni, S, Salvaneschi, L

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Trichothiodystrophy without photosensitivity: biochemical, ultrastructural and DNA repair studies von FOIS, A, BALESTRI, P, CALVIERI, S, ZAMPETTI, M, GIUSTINI, S, STEFANINI, M, LAGOMARSINI, P

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Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy von Stefanini, Miria, Lagomarsini, Paola, Giliani, Silvia, Nardo, Tiziana, Botta, Elena, Peserico, Andrea, Kleijer, Wim J., Lehmann, Alan R., Sarasin, Alain

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Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity von Stefanini, M., Lagomarsini, P., Giorgi, R., Nuzzo, F.

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Normal sensitivity to mutagens, spontaneous chromosome breakage, and mutation frequency in nevoid basal cell carcinoma syndrome von STEFANINI, M, LAGOMARSINI, P, BERARDESCA, E, BORRONI, G, RABBIOSI, G, NUZZO, F

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Chromosomal fragility in the cancer‐prone disease xeroderma pigmentosum preferentially involves bands relevant for cutaneous carcinogenesis von Lanza, Annalisa, Lagomarsini, Paola, Casati, Alessandra, Ghetti, Pierluigi, Stefanini, Miria

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Clonal chromosome rearrangements in a fibroblast strain from a patient affected by xeroderma pigmentosum (complementation group C) von Nuzzo, F., Lagomarsini, P., Casati, A., Giorgi, R., Berardesca, E., Stefanini, M.

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Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophy von Nuzzo, F., Stefanini, M., Rocchi, M., Casati, A., Colognola, R., Lagomarsini, P., Marinoni, S., Scozzari, R.

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The basal and the mutagen-induced levels of ADP-ribosyl transferase activity are not modified in Fanconi's anemia cells von Scovassi, A.I., Stefanini, M., Izzo, R., Lagomarsini, P., Bertazzoni, U., Moustacchi, E.

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Stratification of patients admitted for SARS-CoV2 infection: prognostic scores in the first and second wave of the pandemic von Innocenti, F., De Paris, A., Lagomarsini, A., Pelagatti, L., Casalini, L., Gianno, A., Montuori, M., Bernardini, P., Caldi, F., Tassinari, I., Pini, R.

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Surveillance of hospital-acquired infections in Liguria, Italy: results from a regional prevalence study in adult and paediatric acute-care hospitals von Durando, P, Icardi, G, Ansaldi, F, Crimi, P, Sticchi, C, Compagnino, F, Fabbri, P, Baldelli, I, Bellina, D, Sacco, R, Assensi, M, Cenderello, N, Orengo, G, Oreste, P, Nannini, M, Olivari, C, Campora, O, Vizio, M

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Clinical significance of a carcinogenesis model of colorectal carcinoma von Spisni, R, Faviana, P, Pingitore, R, Castagna, M, Baroncini, R, Biondi, R, Lagomarsini, B, Colizzi, C

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