Sfoglia per Autore
Sur l'inhibition de la biosynthése de la thyroglobuline dans le corps thyroide du rat par l'isoniazide
1982 Monaco, F; De Luca, M; Carducci, Carla; Pontecorvi, A; D'Armiento, Massimino; Roche, J.
Polymerase chain reaction in thyroid clinical practice - Sample preparation and sources: limits, precautions, contamination.
1991 Pontecorvi, Alfredo; Carducci, Carla; A., Farsetti; Sciacchitano, Salvatore
Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy
1991 Carducci, Carla; Leuzzi, Vincenzo; Scuderi, M; DE NEGRI, Am; Gabrieli, Cb; Antonozzi, Italo; Pontecorvi, A.
Analysis of ras-family proto-oncogenes on DNA extracted from tyroid fine needle aspiration samples by the Polymerase Chain Reaction.
1991 Sciacchitano, Salvatore; Carducci, Carla; Alimandi, Maurizio; MARIANI COSTANTINI, R; Nardi, F; Antonozzi, I; Andreoli, M. AND PONTECORVI A.
DNA Elution and Amplification by Polymerase Chain Reaction from Dried Blood Spots.
1992 Carducci, Carla; Ellul, Lorenzo; Antonozzi, Italo; Pontecorvi, Alfredo
Substitution of Leu for Pro-193 in the insulin receptor in a patient with a genetic form of severe insulin resistance.
1993 Carrera, P; Cordera, R; Ferrari, M; Cremonesi, L; Taramelli, R; Andraghetti, G; Carducci, Carla; Dozio, N; Pozza, G; Taylor, Si
Quantitative analysis of 22 amino acids on dried blood spot by HPLC and neonatal reference values.
1996 Carducci, Claudia; Birarelli, M.; Carducci, Carla; Leuzzi, Vincenzo; Moschini, L.; Antonozzi, Italo
LHON mutations in Italian patients affected by multiple sclerosis.
1996 Leuzzi, Vincenzo; Carducci, Carla; Lanza, M; Salvetti, G; Ristori, G; DI GIOVANNI, S; Torroni, A.
Clinical and molecular evaluation of Italian patients affected by Pelizaeus Merzbacher Disease.
1996 Terregino, C.; Cardona, Francesco Carmelo Giovanni; Barbetti, F.; Antonozzi, Italo; Carducci, Carla
Screening of mtDNA mutations in Italian LHON pedigrees.
1996 Carducci, Carla; DE NEGRI, A. M.; Leuzzi, Vincenzo; Terregino, C.; Torella, M.; PIVETTI PEZZI, P.; Antonozzi, Italo
La malattia di Pelizaeus-Merzbacher: dalla clinica alla genetica molecolare. Giornale di Neuropsicofarmacologia 1997; 6: 135-138.
1997 Cardona, Francesco Carmelo Giovanni; Carducci, Carla; Domenicone, D; Rosati, E.
Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP gene
1997 Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola
Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP Gene.
1997 Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola
One European-specific mt-DNA background plays a role in the expression of Leber Hereditary Optic Neuropathy.
1997 Torroni, A; D'Urbano, L; Sellitto, D; Cruciani, Fulvio; Zeviani, M; Carducci, Carla; Leuzzi, Vincenzo; Carelli, V; Barboni, P; DE NEGRI, A; Scozzari, Rosaria
Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP gene.
1997 Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola
LHON mutations in Italian patients affected by multiple sclerosis
1997 Leuzzi, Vincenzo; Carducci, Carla; M., Lanza; Salvetti, Marco; Ristori, Giovanni; S., Digiovanni; A., Torroni
The STR 252 -IVS10 nt 546 - VNTR 7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples.
1997 Cali', F; Dianzani, I; Desviat, Lr; Perez, B; Ugarte, M; Ozguc, M; Seyrantepe, V; Shiloh, Y; Giannattasio, S; Carducci, Carla; Bosco, P; DI LEO, G.
Haplotype and phylogenetic analyses suggest that one European - specific mtDNA background plays a role in the expression of Leber Hereditary Optic Neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
1997 Torroni, A; Petrozzi, M; D'Urbano, L; Sellitto, D; Zeviani, M; Carrara, F; Carducci, Carla; Leuzzi, Vincenzo; Carelli, V; Barboni, P; DE NEGRI, A; Scozzari, Rosaria
Two novel PAH gene mutations detected in Italian PKU patients.
1997 Argiolas, A; Bosco, P; Cali', F; Ceratto, N; Aniello, G; Riva, E; Biasucci, G; Carducci, Carla; Romano, V.
Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays
1999 Chessa, Luciana; Piane, Maria; Prudente, S; Carducci, Carla; Mazzilli, Maria Cristina; Pachi, A; Negrini, M; Narducci, Mg; Russo, G; Frati, Luigi
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Sur l'inhibition de la biosynthése de la thyroglobuline dans le corps thyroide du rat par l'isoniazide | 1982 | Monaco, F; De Luca, M; Carducci, Carla; Pontecorvi, A; D'Armiento, Massimino; Roche, J. | |
| Polymerase chain reaction in thyroid clinical practice - Sample preparation and sources: limits, precautions, contamination. | 1991 | Pontecorvi, Alfredo; Carducci, Carla; A., Farsetti; Sciacchitano, Salvatore | |
| Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy | 1991 | Carducci, Carla; Leuzzi, Vincenzo; Scuderi, M; DE NEGRI, Am; Gabrieli, Cb; Antonozzi, Italo; Pontecorvi, A. | |
| Analysis of ras-family proto-oncogenes on DNA extracted from tyroid fine needle aspiration samples by the Polymerase Chain Reaction. | 1991 | Sciacchitano, Salvatore; Carducci, Carla; Alimandi, Maurizio; MARIANI COSTANTINI, R; Nardi, F; Antonozzi, I; Andreoli, M. AND PONTECORVI A. | |
| DNA Elution and Amplification by Polymerase Chain Reaction from Dried Blood Spots. | 1992 | Carducci, Carla; Ellul, Lorenzo; Antonozzi, Italo; Pontecorvi, Alfredo | |
| Substitution of Leu for Pro-193 in the insulin receptor in a patient with a genetic form of severe insulin resistance. | 1993 | Carrera, P; Cordera, R; Ferrari, M; Cremonesi, L; Taramelli, R; Andraghetti, G; Carducci, Carla; Dozio, N; Pozza, G; Taylor, Si | |
| Quantitative analysis of 22 amino acids on dried blood spot by HPLC and neonatal reference values. | 1996 | Carducci, Claudia; Birarelli, M.; Carducci, Carla; Leuzzi, Vincenzo; Moschini, L.; Antonozzi, Italo | |
| LHON mutations in Italian patients affected by multiple sclerosis. | 1996 | Leuzzi, Vincenzo; Carducci, Carla; Lanza, M; Salvetti, G; Ristori, G; DI GIOVANNI, S; Torroni, A. | |
| Clinical and molecular evaluation of Italian patients affected by Pelizaeus Merzbacher Disease. | 1996 | Terregino, C.; Cardona, Francesco Carmelo Giovanni; Barbetti, F.; Antonozzi, Italo; Carducci, Carla | |
| Screening of mtDNA mutations in Italian LHON pedigrees. | 1996 | Carducci, Carla; DE NEGRI, A. M.; Leuzzi, Vincenzo; Terregino, C.; Torella, M.; PIVETTI PEZZI, P.; Antonozzi, Italo | |
| La malattia di Pelizaeus-Merzbacher: dalla clinica alla genetica molecolare. Giornale di Neuropsicofarmacologia 1997; 6: 135-138. | 1997 | Cardona, Francesco Carmelo Giovanni; Carducci, Carla; Domenicone, D; Rosati, E. | |
| Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP gene | 1997 | Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola | |
| Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP Gene. | 1997 | Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola | |
| One European-specific mt-DNA background plays a role in the expression of Leber Hereditary Optic Neuropathy. | 1997 | Torroni, A; D'Urbano, L; Sellitto, D; Cruciani, Fulvio; Zeviani, M; Carducci, Carla; Leuzzi, Vincenzo; Carelli, V; Barboni, P; DE NEGRI, A; Scozzari, Rosaria | |
| Proton MR spectroscopy in Pelizaeus-Merzbacher disease without point mutation in PLP gene. | 1997 | Parisi, Pasquale; Spalice, A.; Raucci, U.; Carducci, Carla; Iannetti, Paola | |
| LHON mutations in Italian patients affected by multiple sclerosis | 1997 | Leuzzi, Vincenzo; Carducci, Carla; M., Lanza; Salvetti, Marco; Ristori, Giovanni; S., Digiovanni; A., Torroni | |
| The STR 252 -IVS10 nt 546 - VNTR 7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples. | 1997 | Cali', F; Dianzani, I; Desviat, Lr; Perez, B; Ugarte, M; Ozguc, M; Seyrantepe, V; Shiloh, Y; Giannattasio, S; Carducci, Carla; Bosco, P; DI LEO, G. | |
| Haplotype and phylogenetic analyses suggest that one European - specific mtDNA background plays a role in the expression of Leber Hereditary Optic Neuropathy by increasing the penetrance of the primary mutations 11778 and 14484 | 1997 | Torroni, A; Petrozzi, M; D'Urbano, L; Sellitto, D; Zeviani, M; Carrara, F; Carducci, Carla; Leuzzi, Vincenzo; Carelli, V; Barboni, P; DE NEGRI, A; Scozzari, Rosaria | |
| Two novel PAH gene mutations detected in Italian PKU patients. | 1997 | Argiolas, A; Bosco, P; Cali', F; Ceratto, N; Aniello, G; Riva, E; Biasucci, G; Carducci, Carla; Romano, V. | |
| Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays | 1999 | Chessa, Luciana; Piane, Maria; Prudente, S; Carducci, Carla; Mazzilli, Maria Cristina; Pachi, A; Negrini, M; Narducci, Mg; Russo, G; Frati, Luigi |
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