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.
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
MANAGEMENT OF SMALL RENAL CANCER IN A CONTEMPORARY SERIES OF PATIENTS WITH VON HIPPEL-LINDAU DISEASE.
2011-01-01 Destefanis P; Lucatello B; Maccario M; Veltri A; Pasini B; Carchedi M; Buffardi A; Travaglini F; Battaglia A; Bisconti A; Bosio A; Lillaz B; Fontana D.
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. | |
| 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 | |
| MANAGEMENT OF SMALL RENAL CANCER IN A CONTEMPORARY SERIES OF PATIENTS WITH VON HIPPEL-LINDAU DISEASE. | 2011 | Destefanis P; Lucatello B; Maccario M; Veltri A; Pasini B; Carchedi M; Buffardi A; Travaglini F; Battaglia A; Bisconti A; Bosio A; Lillaz B; Fontana D. | |
| 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. |