Cappellacci S - Search Results

1

Sirenomelia and VACTERL association in the offspring of a woman with diabetes.

Castori M, Silvestri E, Cappellacci S, Binni F, Sforzolini GS, Grammatico P. Castori M, et al. Among authors: cappellacci s. Am J Med Genet A. 2010 Jul;152A(7):1803-7. doi: 10.1002/ajmg.a.33460. Am J Med Genet A. 2010. PMID: 20583159

2

Tibial developmental field defect is the most common lower limb malformation pattern in VACTERL association.

Castori M, Rinaldi R, Cappellacci S, Grammatico P. Castori M, et al. Among authors: cappellacci s. Am J Med Genet A. 2008 May 15;146A(10):1259-66. doi: 10.1002/ajmg.a.32288. Am J Med Genet A. 2008. PMID: 18386801 Review.

3

De novo pure 12q22q24.33 duplication: first report of a case with mental retardation, ADHD, and Dandy-Walker malformation.

Cappellacci S, Martinelli S, Rinaldi R, Martinelli E, Parisi P, Mancini B, Pescosolido R, Grammatico P. Cappellacci S, et al. Am J Med Genet A. 2006 Jun 1;140(11):1203-7. doi: 10.1002/ajmg.a.31219. Am J Med Genet A. 2006. PMID: 16652357

4

A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotype.

Cecconi M, Forzano F, Rinaldi R, Cappellacci S, Grammatico P, Faravelli F, Dagna Bricarelli F, Di Maria E, Grasso M. Cecconi M, et al. Among authors: cappellacci s. J Mol Diagn. 2008 May;10(3):272-5. doi: 10.2353/jmoldx.2008.070163. Epub 2008 Apr 10. J Mol Diagn. 2008. PMID: 18403614 Free PMC article.

5

The antigen processing machinery of class I human leukocyte antigens: linked patterns of gene expression in neoplastic cells.

Giorda E, Sibilio L, Martayan A, Moretti S, Venturo I, Mottolese M, Ferrara GB, Cappellacci S, Eibenschutz L, Catricalà C, Grammatico P, Giacomini P. Giorda E, et al. Among authors: cappellacci s. Cancer Res. 2003 Jul 15;63(14):4119-27. Cancer Res. 2003. PMID: 12874016

6

A melanoma immune response signature including Human Leukocyte Antigen-E.

Tremante E, Ginebri A, Lo Monaco E, Benassi B, Frascione P, Grammatico P, Cappellacci S, Catricalà C, Arcelli D, Natali PG, Di Filippo F, Mottolese M, Visca P, Benevolo M, Giacomini P. Tremante E, et al. Among authors: cappellacci s. Pigment Cell Melanoma Res. 2014 Jan;27(1):103-12. doi: 10.1111/pcmr.12164. Epub 2013 Oct 9. Pigment Cell Melanoma Res. 2014. PMID: 24011128 Clinical Trial.

7

HLA-DR and -DQ alleles in Italian patients with melanoma.

Lulli P, Grammatico P, Brioli G, Catricalà C, Morellini M, Roccella M, Mariani B, Pennesi G, Roccella F, Cappellacci S, Trabace S. Lulli P, et al. Among authors: cappellacci s. Tissue Antigens. 1998 Mar;51(3):276-80. doi: 10.1111/j.1399-0039.1998.tb03102.x. Tissue Antigens. 1998. PMID: 9550328

8

cDNA-array profiling of melanomas and paired melanocyte cultures.

Mischiati C, Natali PG, Sereni A, Sibilio L, Giorda E, Cappellacci S, Nicotra MR, Mariani G, Di Filippo F, Catricalà C, Gambari R, Grammatico P, Giacomini P. Mischiati C, et al. Among authors: cappellacci s. J Cell Physiol. 2006 Jun;207(3):697-705. doi: 10.1002/jcp.20610. J Cell Physiol. 2006. PMID: 16523488

9

A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia.

Borriello A, Locasciulli A, Bianco AM, Criscuolo M, Conti V, Grammatico P, Cappellacci S, Zatterale A, Morgese F, Cucciolla V, Delia D, Della Ragione F, Savoia A. Borriello A, et al. Among authors: cappellacci s. Leukemia. 2007 Jan;21(1):72-8. doi: 10.1038/sj.leu.2404468. Epub 2006 Nov 9. Leukemia. 2007. PMID: 17096012

10

Psoriatic arthritis: a clinical, radiological and genetic study of 58 Italian patients.

Trabace S, Cappellacci S, Ciccarone P, Liaskos S, Polito R, Zorzin L. Trabace S, et al. Among authors: cappellacci s. Acta Derm Venereol Suppl (Stockh). 1994;186:69-70. Acta Derm Venereol Suppl (Stockh). 1994. PMID: 8073843

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