Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

388 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Adult Wilms' tumor: A monoinstitutional experience and a review of the literature.
Terenziani M, Spreafico F, Collini P, Piva L, Perotti D, Podda M, Gandola L, Massimino M, Cereda S, Cefalo G, Luksch R, Casanova M, Ferrari A, Polastri D, Valagussa P, Fossati-Bellani F. Terenziani M, et al. Among authors: collini p. Cancer. 2004 Jul 15;101(2):289-93. doi: 10.1002/cncr.20387. Cancer. 2004. PMID: 15241825 Free article. Review.
Bilateral preaxial polydactyly in a WAGR syndrome patient.
Manoukian S, Crolla JA, Mammoliti PM, Testi MA, Zanini R, Carpanelli ML, Piozzi E, Sozzi G, De Vecchi G, Terenziani M, Spreafico F, Collini P, Radice P, Perotti D. Manoukian S, et al. Among authors: collini p. Am J Med Genet A. 2005 May 1;134(4):426-9. doi: 10.1002/ajmg.a.30647. Am J Med Genet A. 2005. PMID: 15742368
Endodermal sinus tumor of the vagina.
Terenziani M, Spreafico F, Collini P, Meazza C, Massimino M, Piva L. Terenziani M, et al. Among authors: collini p. Pediatr Blood Cancer. 2007 May;48(5):577-8. doi: 10.1002/pbc.20636. Pediatr Blood Cancer. 2007. PMID: 16200632
Non-chromosome 11-p syndromes in Wilms tumor patients: Clinical and cytogenetic report of two Down syndrome cases and one Turner syndrome case.
Spreafico F, Terenziani M, Lualdi E, Scarfone P, Collini P, Fossati-Bellani F, Galea E, De Vecchi G, Sardella M, Sozzi G, Radice P, Perotti D. Spreafico F, et al. Among authors: collini p. Am J Med Genet A. 2007 Jan 1;143A(1):85-8. doi: 10.1002/ajmg.a.31480. Am J Med Genet A. 2007. PMID: 17163536 No abstract available.
The murine Pou6f2 gene is temporally and spatially regulated during kidney embryogenesis and its human homolog is overexpressed in a subset of Wilms tumors.
Di Renzo F, Doneda L, Menegola E, Sardella M, De Vecchi G, Collini P, Spreafico F, Fossati-Bellani F, Giavini E, Radice P, Perotti D. Di Renzo F, et al. Among authors: collini p. J Pediatr Hematol Oncol. 2006 Dec;28(12):791-7. doi: 10.1097/MPH.0b013e31802d3e65. J Pediatr Hematol Oncol. 2006. PMID: 17164647
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.
Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A. Cerrato F, et al. Among authors: collini p. Hum Mol Genet. 2008 May 15;17(10):1427-35. doi: 10.1093/hmg/ddn031. Epub 2008 Feb 1. Hum Mol Genet. 2008. PMID: 18245780 Free article.
388 results