Sfoglia per Autore
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms
1998-01-01 Minelli, Antonella; Capra, E.; Dellavecchia, C.; Danesino, Cesare; Olivieri, Carla; Tateo, S.; Tenti, P.; Scappaticci, MARIA ASSUNTA
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer.
1999-01-01 Scappaticci, MARIA ASSUNTA; Pasquali, Francesco; Capra, E; Olivieri, Carla; Tateo, S.
Early onset of gastric carcinoma and constitutional deletion of 18p.
1999-01-01 Dellavecchia, C; Guala, A; Olivieri, Carla; Haintink, O; Cadario, F; Luinetti, O; Fiocca, R; Minelli, Antonella; Danesino, Cesare; Bona, G.
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders
2000-01-01 Maserati, E.; Minelli, Antonella; Olivieri, Carla; Bonvini, L.; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F.
FAMILIAL PARTIAL MONOSOMY 7 AND MYELODYSPLASIA: DIFFERENT PARENTAL ORIGIN OF THE 7 INVOLVED SUGGESTS THE ACTION OF A MUTATOR GENE
2000-01-01 Minelli, Antonella; Maserati, E; Giudici, G; Tosi, S; Olivieri, Carla; Bonvini, L.; DE FILIPPI, Paola; Biondi, A.; LO CURTO, F.; Pasquali, F.; Danesino, Cesare
Isochromosome 7q10 in Shwachman Syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
2000-01-01 Maserati, E; Minelli, Antonella; Olivieri, Carla; Bonvini, L; Marchi, A; Bozzola, Mauro; Danesino, Cesare; Mariani, Enrica; Pasquali, F.
Cytogenetic and molecular data in familial myelodysplastic syndrome associated with monosomy 7.
2000-01-01 Danesino, Cesare; Minelli, Antonella; Maserati, E; Guidici, A; De Filippi, F; Olivieri, Carla; Tosi, S; Bonvini, L; Lo Curto, F; Biondi, A; Pasquali, F.
Analisi di linkage in 4 famiglie con Rendu Weber Osler.
2000-01-01 Danesino, Cesare; Olivieri, Carla; Dely, G; Mira, Eugenio
Isochromosome (7) (q10) in Schwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders.
2000-01-01 Maserati, E; Minelli, Antonella; Olivieri, Carla; Bonvini, L; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F.
Erythroleukaemia with tetrasomy 21 in a child without Down phenotype: evidence for a meiotic origin.
2000-01-01 Danesino, Cesare; Pasquali, F; Maserati, E; Panarello, C; Minelli, Antonella; Olivieri, Carla; Morerio, C; Bonvini, L; Russo, I; Rapella, A; Rosanda, C.
Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia
2001-01-01 Minelli, Antonella; Morerio, C.; Maserati, E.; Olivieri, Carla; Panarello, C.; Bonvini, L.; Leszl, A.; Rosanda, C.; Lanino, E.; Danesino, C.; Pasquali, F.
Familial partial monosomy 7 suggests action of a mutator gene.
2001-01-01 Danesino, Cesare; Minelli, Antonella; Maserati, E; Giudici, G; Tosi, S; Olivieri, Carla; Bonvini, L; De Filippi, P; Biondi, A; Lo Curto, F; Pasquali, F.
Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukemia.
2001-01-01 Danesino, Cesare; Minelli, Antonella; Morerio, C; Olivieri, Carla; Panarello, C; Bonvini, L; Leszl, A; Rosanda, C; Lanino, C; Pasquali, F.
Familial partial monosomy 7 and myelodysplasia : different parental origin of the monosomy 7 suggests action of a mutator gene
2001-01-01 Minelli, Antonella; Maserati, E.; Giudici, G.; Tosi, S.; Olivieri, Carla; Bonvini, L.; DE FILIPPI, P.; Biondi, A.; LO CURTO, F.; Pasquali, F.; Danesino, Cesare
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome
2002-01-01 Lisi, V; Guala, A; Lopez, A; Vitali, M; Spadoni, E; Olivieri, Carla; Danesino, Cesare; Mottes, M.
Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia
2002-01-01 Olivieri, Carla; Mira, E; Delu, G; Pagella, F; Zambelli, A; Malvezzi, L; Buscarini, E; Danesino, Cesare
Interstitial deletion of chromsome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.
2003-01-01 Olivieri, Carla; Maraschio, Paola; D., Caselli; C., Martini; G., Beluffi; E., Maserati; Danesino, Cesare
High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia
2004-01-01 Buscarini, E.; Danesino, Cesare; Plauchu, H.; DE FAZIO, C.; Olivieri, Carla; Brambilla, G.; Menozzi, F.; Reduzzi, L.; Blotta, P.; Gazzaniga, P.; Pagella, F.; Grosso, M.; Pongiglione, G.; Cappiello, J.; Zambelli, A.
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children?
2004-01-01 Olivieri, Carla; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Bozzola, Mauro
Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia - results of extensive screening.
2004-01-01 Buscarini, E.; Danesino, Cesare; Olivieri, Carla; Lupinacci, G.; DE GRAZIA, F.; Reduzzi, L.; Blotta, P.; Gazzaniga, P.; Pagella, F.; Grosso, M.; Pongiglione, G.; Buscarini, L.; Plauchu, H.; Zambelli, A.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Concurrent cytogenetic and molecular investigations in uterine and ovarian neoplasms | 1-gen-1998 | Minelli, Antonella; Capra, E.; Dellavecchia, C.; Danesino, Cesare; Olivieri, Carla; Tateo, S.; Tenti, P.; Scappaticci, MARIA ASSUNTA | |
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. | 1-gen-1999 | Scappaticci, MARIA ASSUNTA; Pasquali, Francesco; Capra, E; Olivieri, Carla; Tateo, S. | |
Early onset of gastric carcinoma and constitutional deletion of 18p. | 1-gen-1999 | Dellavecchia, C; Guala, A; Olivieri, Carla; Haintink, O; Cadario, F; Luinetti, O; Fiocca, R; Minelli, Antonella; Danesino, Cesare; Bona, G. | |
Isochromosome (7)(q10) in Shwachman Syndrome Without MDS/AML and Role of Chromosome 7 Anomalies in Myeloproliferative Disorders | 1-gen-2000 | Maserati, E.; Minelli, Antonella; Olivieri, Carla; Bonvini, L.; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F. | |
FAMILIAL PARTIAL MONOSOMY 7 AND MYELODYSPLASIA: DIFFERENT PARENTAL ORIGIN OF THE 7 INVOLVED SUGGESTS THE ACTION OF A MUTATOR GENE | 1-gen-2000 | Minelli, Antonella; Maserati, E; Giudici, G; Tosi, S; Olivieri, Carla; Bonvini, L.; DE FILIPPI, Paola; Biondi, A.; LO CURTO, F.; Pasquali, F.; Danesino, Cesare | |
Isochromosome 7q10 in Shwachman Syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders. | 1-gen-2000 | Maserati, E; Minelli, Antonella; Olivieri, Carla; Bonvini, L; Marchi, A; Bozzola, Mauro; Danesino, Cesare; Mariani, Enrica; Pasquali, F. | |
Cytogenetic and molecular data in familial myelodysplastic syndrome associated with monosomy 7. | 1-gen-2000 | Danesino, Cesare; Minelli, Antonella; Maserati, E; Guidici, A; De Filippi, F; Olivieri, Carla; Tosi, S; Bonvini, L; Lo Curto, F; Biondi, A; Pasquali, F. | |
Analisi di linkage in 4 famiglie con Rendu Weber Osler. | 1-gen-2000 | Danesino, Cesare; Olivieri, Carla; Dely, G; Mira, Eugenio | |
Isochromosome (7) (q10) in Schwachman syndrome without MDS/AML and role of chromosome 7 anomalies in myeloproliferative disorders. | 1-gen-2000 | Maserati, E; Minelli, Antonella; Olivieri, Carla; Bonvini, L; Marchi, Antonietta; Bozzola, Mauro; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Pasquali, F. | |
Erythroleukaemia with tetrasomy 21 in a child without Down phenotype: evidence for a meiotic origin. | 1-gen-2000 | Danesino, Cesare; Pasquali, F; Maserati, E; Panarello, C; Minelli, Antonella; Olivieri, Carla; Morerio, C; Bonvini, L; Russo, I; Rapella, A; Rosanda, C. | |
Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia | 1-gen-2001 | Minelli, Antonella; Morerio, C.; Maserati, E.; Olivieri, Carla; Panarello, C.; Bonvini, L.; Leszl, A.; Rosanda, C.; Lanino, E.; Danesino, C.; Pasquali, F. | |
Familial partial monosomy 7 suggests action of a mutator gene. | 1-gen-2001 | Danesino, Cesare; Minelli, Antonella; Maserati, E; Giudici, G; Tosi, S; Olivieri, Carla; Bonvini, L; De Filippi, P; Biondi, A; Lo Curto, F; Pasquali, F. | |
Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukemia. | 1-gen-2001 | Danesino, Cesare; Minelli, Antonella; Morerio, C; Olivieri, Carla; Panarello, C; Bonvini, L; Leszl, A; Rosanda, C; Lanino, C; Pasquali, F. | |
Familial partial monosomy 7 and myelodysplasia : different parental origin of the monosomy 7 suggests action of a mutator gene | 1-gen-2001 | Minelli, Antonella; Maserati, E.; Giudici, G.; Tosi, S.; Olivieri, Carla; Bonvini, L.; DE FILIPPI, P.; Biondi, A.; LO CURTO, F.; Pasquali, F.; Danesino, Cesare | |
Linkage analysis for prenatal diagnosis in a familial case of Stickler syndrome | 1-gen-2002 | Lisi, V; Guala, A; Lopez, A; Vitali, M; Spadoni, E; Olivieri, Carla; Danesino, Cesare; Mottes, M. | |
Identification of 13 new mutations in the ACVRL1 gene in a group of 52 unselected Italian patients affected by hereditary haemorrhagic telangiectasia | 1-gen-2002 | Olivieri, Carla; Mira, E; Delu, G; Pagella, F; Zambelli, A; Malvezzi, L; Buscarini, E; Danesino, Cesare | |
Interstitial deletion of chromsome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome. | 1-gen-2003 | Olivieri, Carla; Maraschio, Paola; D., Caselli; C., Martini; G., Beluffi; E., Maserati; Danesino, Cesare | |
High prevalence of hepatic focal nodular hyperplasia in subjects with hereditary hemorrhagic telangiectasia | 1-gen-2004 | Buscarini, E.; Danesino, Cesare; Plauchu, H.; DE FAZIO, C.; Olivieri, Carla; Brambilla, G.; Menozzi, F.; Reduzzi, L.; Blotta, P.; Gazzaniga, P.; Pagella, F.; Grosso, M.; Pongiglione, G.; Cappiello, J.; Zambelli, A. | |
Can GH induce chromosome breaks or microsatellite instability in GH-deficient children? | 1-gen-2004 | Olivieri, Carla; Danesino, Cesare; Scappaticci, MARIA ASSUNTA; Bozzola, Mauro | |
Doppler ultrasonographic grading of hepatic vascular malformations in hereditary hemorrhagic telangiectasia - results of extensive screening. | 1-gen-2004 | Buscarini, E.; Danesino, Cesare; Olivieri, Carla; Lupinacci, G.; DE GRAZIA, F.; Reduzzi, L.; Blotta, P.; Gazzaniga, P.; Pagella, F.; Grosso, M.; Pongiglione, G.; Buscarini, L.; Plauchu, H.; Zambelli, A. |
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