Dalprà L - Search Results

1

A new human cell line, PDSS-26, from poorly differentiated synovial sarcoma, with unique chromosomal anomalies.

Berardi AC, Parafioriti A, Barisani D, Papp B, Armiraglio E, Martinoli M, Dalprà L, Santoro A. Berardi AC, et al. Among authors: dalpra l. Cancer Genet Cytogenet. 2003 Oct 15;146(2):116-24. doi: 10.1016/s0165-4608(03)00135-3. Cancer Genet Cytogenet. 2003. PMID: 14553945

2

Endometrioid-like yolk sac and Sertoli-Leydig cell tumors in a carrier of a Y heterochromatin insertion into 1qh region: a causal association?

Sala E, Villa N, Crosti F, Miozzo M, Perego P, Cappellini A, Bonazzi C, Barisani D, Dalprà L. Sala E, et al. Among authors: dalpra l. Cancer Genet Cytogenet. 2007 Mar;173(2):164-9. doi: 10.1016/j.cancergencyto.2006.10.014. Cancer Genet Cytogenet. 2007. PMID: 17321334

3

Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis.

Riva P, Crosti F, Orzan F, Dalprà L, Mortini P, Parafioriti A, Pollo B, Fuhrman Conti AM, Miozzo M, Larizza L. Riva P, et al. Among authors: dalpra l. Int J Cancer. 2003 Nov 10;107(3):493-7. doi: 10.1002/ijc.11421. Int J Cancer. 2003. PMID: 14506752

4

19p deletion in recurring leiomyosarcoma lesions from the same patient.

Riva P, Dalprá L, Gualandri V, Volontè M, Miozzo M, Malgara R, Conti AF, Larizza L. Riva P, et al. Among authors: dalpra l. Cancer Genet Cytogenet. 2000 Jun;119(2):102-8. doi: 10.1016/s0165-4608(99)00222-8. Cancer Genet Cytogenet. 2000. PMID: 10867143

5

Lymph node hyperplasia: clonal chromosomal and genomic rearrangements. Report of two new cases and literature review.

Villa N, Redaelli S, Lissoni S, Saccheri F, Sala E, Crosti F, Dalprà L, Carrino V, Pioltelli P, Isimbaldi G. Villa N, et al. Among authors: dalpra l. Cancer Genet. 2014 Jan-Feb;207(1-2):12-8. doi: 10.1016/j.cancergen.2014.01.003. Epub 2014 Jan 16. Cancer Genet. 2014. PMID: 24636528 Review.

6

Clinical and genetic familial study of a large cohort of Italian children with idiopathic epilepsy.

Combi R, Grioni D, Contri M, Redaelli S, Redaelli F, Bassi MT, Barisani D, Lavitrano ML, Tredici G, Tenchini ML, Bertolini M, Dalprà L. Combi R, et al. Among authors: dalpra l. Brain Res Bull. 2009 Apr 29;79(2):89-96. doi: 10.1016/j.brainresbull.2009.01.008. Epub 2009 Feb 5. Brain Res Bull. 2009. PMID: 19200853

7

Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome.

Miozzo M, Castorina P, Riva P, Dalprà L, Fuhrman Conti AM, Volpi L, Hoe TS, Khoo A, Wiegant J, Rosenberg C, Larizza L. Miozzo M, et al. Among authors: dalpra l. Int J Cancer. 1998 Aug 12;77(4):504-10. doi: 10.1002/(sici)1097-0215(19980812)77:4<504::aid-ijc5>3.0.co;2-y. Int J Cancer. 1998. PMID: 9679749

8

Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.

Marozzi A, Manfredini E, Tibiletti MG, Furlan D, Villa N, Vegetti W, Crosignani PG, Ginelli E, Meneveri R, Dalprà L. Marozzi A, et al. Among authors: dalpra l. Hum Genet. 2000 Oct;107(4):304-11. doi: 10.1007/s004390000364. Hum Genet. 2000. PMID: 11129329

9

Are chromosome aberrations in circulating lymphocytes predictive of future cancer onset in humans? Preliminary results of an Italian cohort study.

Bonassi S, Abbondandolo A, Camurri L, Dal Prá L, De Ferrari M, Degrassi F, Forni A, Lamberti L, Lando C, Padovani P, et al. Bonassi S, et al. Cancer Genet Cytogenet. 1995 Feb;79(2):133-5. doi: 10.1016/0165-4608(94)00131-t. Cancer Genet Cytogenet. 1995. PMID: 7889505

10

Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements.

Portera G, Venturin M, Patrizi A, Martinoli E, Riva P, Dalprà L. Portera G, et al. Among authors: dalpra l. J Hum Genet. 2006;51(1):68-75. doi: 10.1007/s10038-005-0326-9. Epub 2005 Dec 3. J Hum Genet. 2006. PMID: 16328081

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