PASINI, Barbara
PASINI, Barbara
SCIENZE MEDICHE
A case of medullary thyroid carcinoma, parathyroid focal hyperplasia and pancreatic neuroendocrine tumor without RET and MEN1 mutations
2008-01-01 Pasini B; Ferrando B; Menegatti E; Casalis Cavalchini G; Ricci MT; Asioli S; Bussolati G; De Angelis G; Bisbocci D
A germline mismatch repair mutation possibly leading to a de novo NF1 germline mutation.
2014-01-01 Bracco C; Borelli I; Micheletti M; Martorana D;Grosso E; Pasini B
Acromegaly and Familial Paragangliomas: A New Syndrome?
2010-01-01 Xekouki P; Azevedo MF; Pasini B; Lytras A; Lange E; Keil M; Pacak K; Horvath A; Tolis G; Stratakis CA.
Analisi genetica del gene CYP21 in forme non classiche di deficit di 21-beta-idrossilasi
2008-01-01 F. Restivo; E. Napolitano; C. Manieri; S. Einaudi; B. Pasini; E. Menegatti
Bi-allelic MSH6 mutations in a case of early onset multiple primary tumors resembling Lynch and Turcot syndrome
2014-01-01 G. C. Casalis Cavalchini; D. Giachino; G. Mandrile; I. Borelli; M. Micheletti; T. Venesio; M. De Marchi; B. Pasini
BRCA1 and BRCA2 germline mutations in early-onset breast carcinoma patients.
1998-01-01 Conti AR; De Benedetti MVG; Stagi L; Mondini P; Pasini B; Pensotti V; Spatti GB; Rilke F; Pierotti MA; Radice P.
Do Chromosome 17 Centromere Copy Numbers Predict Polysomy? A Fluorescence In Situ Hybridization and Microarray-Based CGH Analysis.
2009-01-01 Marchiò C; Lambros MBK; Gugliotta P; Di Cantogno L. Verdun; Botta C; Pasini B; Shiu KK; Mackay A; Fenwick K; Tamber N; Ashworth A; Sapino A; Reis-Filho JS.
Extending the Benign and Malignant Phenotypes Associated with Germline DICER1 Mutations.
2011-01-01 Tischkowitz M; Bahubeshi A; Hamel N; Pasini B; Asioli S; Baynam G; Overkov A; Frieder RP; Dishop M; Graf N; Ekim M; Bouron-Dal Soglio D; Arseneau J; Young RH; Sabbaghian N; Srivastava A; Priest JR; Foulkes WD.
High frequency of genetic variants in DNA repair genes in patients with multiple primary tumors and/or belonging to families with cluster of infrequent cancers
2015-01-01 Casalone Elisabetta, Vignolo Lutati Francesca, Bracco Cecilia, Casalis Cavalchini Guido Claudio, Ogliara Paola, Ferrando Barbara, Russo Alessia, Mandrile Giorgia, Candita Luisa, Majore Silvia, Grammatico Paola, Genuardi Maurizio, Matullo Giuseppe, Pasini Barbara
Histopathology of ovarian tumors in women with BRCA1 and 2 mutations.
2003-01-01 Carcangiu ML; Radice P; Spatti G; Manoukian S; Pasini B.
Incidental tumors in prophylactic oophorectomy specimens from BRCA mutation carriers.
2003-01-01 Carcangiu ML; Radice P; Spatti G; Manoukian S; Pasini B.
Management of renal cancer in a contemporary series of patients affected by Von Hippel-Lindau disease.
2013-01-01 P. Destefanis; B. Lucatello; M. Maccario; A. Veltri; B. Pasini; A. Battaglia; M. Allasia; A. Gonella; A. Bosio; B. Lillaz; B. Frea; D. Fontana
Management of small renal cancer in a contemporary series of patients affected by Von Hippel-Lindau disease.
2011-01-01 P. Destefanis; B. Lucatello; M. Maccario; A. Veltri; B. Pasini; M. Carchedi; A. Buffardi; A. Bisconti; A. Bosio; B. Lillaz; D. Fontana
Mutation analysis of the MSH6 gene in 52 MLH1/MSH2-negative, HNPCC suspect Italian patients
2006-01-01 P. Pazienza*; M. Barberis*; I. Borelli; S. Regazzoni; D. Giachino; G. Casalis Cavalchini; A. Allavena; M. Micheletti; A. Arrigoni; M. Schena; E. Grosso; T. Venesio; E. David; B. Pasini; N. Migone; M. De Marchi
Screening for BRCA1 and BRCA2 germ line point mutations in 600 Italian families with breast and/or ovarian cancer: mutation prevalence according to phenotype.
2003-01-01 Pasini B; Manoukian S; Pensotti V; Crucianelli R; Spatti GB; Conti RA; Genovese T; Peissel B; Mariani L; Merola M; Cavalchini GC; Pierotti MA; Radice P.
Two new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations identified in a cohort of Italian breast and ovarian cancer families.
2014-01-01 Vignolo Lutati F; Casalis Cavalchini G; Sapino A; Pasini B
Unusual association of pancreatic neuroendocrine tumors and papillary renal cell cancer.
2008-01-01 Pasini B; Ferrando B; Menegatti E; Casalis Cavalchini G; Ricci MT; Asioli S; Bussolati G; De Angelis C; Campra D; Porta M
X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families.
2003-01-01 Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A case of medullary thyroid carcinoma, parathyroid focal hyperplasia and pancreatic neuroendocrine tumor without RET and MEN1 mutations | 2008 | Pasini B; Ferrando B; Menegatti E; Casalis Cavalchini G; Ricci MT; Asioli S; Bussolati G; De Angelis G; Bisbocci D | |
| A germline mismatch repair mutation possibly leading to a de novo NF1 germline mutation. | 2014 | Bracco C; Borelli I; Micheletti M; Martorana D;Grosso E; Pasini B | |
| Acromegaly and Familial Paragangliomas: A New Syndrome? | 2010 | Xekouki P; Azevedo MF; Pasini B; Lytras A; Lange E; Keil M; Pacak K; Horvath A; Tolis G; Stratakis CA. | |
| Analisi genetica del gene CYP21 in forme non classiche di deficit di 21-beta-idrossilasi | 2008 | F. Restivo; E. Napolitano; C. Manieri; S. Einaudi; B. Pasini; E. Menegatti | |
| Bi-allelic MSH6 mutations in a case of early onset multiple primary tumors resembling Lynch and Turcot syndrome | 2014 | G. C. Casalis Cavalchini; D. Giachino; G. Mandrile; I. Borelli; M. Micheletti; T. Venesio; M. De Marchi; B. Pasini | |
| BRCA1 and BRCA2 germline mutations in early-onset breast carcinoma patients. | 1998 | Conti AR; De Benedetti MVG; Stagi L; Mondini P; Pasini B; Pensotti V; Spatti GB; Rilke F; Pierotti MA; Radice P. | |
| Do Chromosome 17 Centromere Copy Numbers Predict Polysomy? A Fluorescence In Situ Hybridization and Microarray-Based CGH Analysis. | 2009 | Marchiò C; Lambros MBK; Gugliotta P; Di Cantogno L. Verdun; Botta C; Pasini B; Shiu KK; Mackay A; Fenwick K; Tamber N; Ashworth A; Sapino A; Reis-Filho JS. | |
| Extending the Benign and Malignant Phenotypes Associated with Germline DICER1 Mutations. | 2011 | Tischkowitz M; Bahubeshi A; Hamel N; Pasini B; Asioli S; Baynam G; Overkov A; Frieder RP; Dishop M; Graf N; Ekim M; Bouron-Dal Soglio D; Arseneau J; Young RH; Sabbaghian N; Srivastava A; Priest JR; Foulkes WD. | |
| High frequency of genetic variants in DNA repair genes in patients with multiple primary tumors and/or belonging to families with cluster of infrequent cancers | 2015 | Casalone Elisabetta, Vignolo Lutati Francesca, Bracco Cecilia, Casalis Cavalchini Guido Claudio, Ogliara Paola, Ferrando Barbara, Russo Alessia, Mandrile Giorgia, Candita Luisa, Majore Silvia, Grammatico Paola, Genuardi Maurizio, Matullo Giuseppe, Pasini Barbara | |
| Histopathology of ovarian tumors in women with BRCA1 and 2 mutations. | 2003 | Carcangiu ML; Radice P; Spatti G; Manoukian S; Pasini B. | |
| Incidental tumors in prophylactic oophorectomy specimens from BRCA mutation carriers. | 2003 | Carcangiu ML; Radice P; Spatti G; Manoukian S; Pasini B. | |
| Management of renal cancer in a contemporary series of patients affected by Von Hippel-Lindau disease. | 2013 | P. Destefanis; B. Lucatello; M. Maccario; A. Veltri; B. Pasini; A. Battaglia; M. Allasia; A. Gonella; A. Bosio; B. Lillaz; B. Frea; D. Fontana | |
| Management of small renal cancer in a contemporary series of patients affected by Von Hippel-Lindau disease. | 2011 | P. Destefanis; B. Lucatello; M. Maccario; A. Veltri; B. Pasini; M. Carchedi; A. Buffardi; A. Bisconti; A. Bosio; B. Lillaz; D. Fontana | |
| Mutation analysis of the MSH6 gene in 52 MLH1/MSH2-negative, HNPCC suspect Italian patients | 2006 | P. Pazienza*; M. Barberis*; I. Borelli; S. Regazzoni; D. Giachino; G. Casalis Cavalchini; A. Allavena; M. Micheletti; A. Arrigoni; M. Schena; E. Grosso; T. Venesio; E. David; B. Pasini; N. Migone; M. De Marchi | |
| Screening for BRCA1 and BRCA2 germ line point mutations in 600 Italian families with breast and/or ovarian cancer: mutation prevalence according to phenotype. | 2003 | Pasini B; Manoukian S; Pensotti V; Crucianelli R; Spatti GB; Conti RA; Genovese T; Peissel B; Mariani L; Merola M; Cavalchini GC; Pierotti MA; Radice P. | |
| Two new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations identified in a cohort of Italian breast and ovarian cancer families. | 2014 | Vignolo Lutati F; Casalis Cavalchini G; Sapino A; Pasini B | |
| Unusual association of pancreatic neuroendocrine tumors and papillary renal cell cancer. | 2008 | Pasini B; Ferrando B; Menegatti E; Casalis Cavalchini G; Ricci MT; Asioli S; Bussolati G; De Angelis C; Campra D; Porta M | |
| X-linked Charcot-Marie-Tooth polyneuropathy due to mutation of the connexin-32 gene: revision of our cases of genetic neuropathies and identification of three affected families. | 2003 | Vercelli M; Mongini T; Pasini B; Cocito D; Benna P; Benetton G; Mutani R; Palmucci L. |