Publications by authors named "Vallo Laura"

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Detection of an unstable non-coding tandem repeat in the ZNF291 gene.
Vallo Laura, Bonifazi Emanuela, Angelini Corrado, Novelli Giuseppe, Botta Annalisa

Mol Cell Probes· December 2007

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Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.
Annalisa Botta, Laura Vallo, Fabrizio Rinaldi, Emanuela Bonifazi, Francesca Amati

Gene Expr· September 2007

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Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients.
Leila Baghernajad Salehi, Emanuela Bonifazi, Enrico Di Stasio, Massimo Gennarelli, Annalisa Botta, Laura Vallo

Genet Test· May 2007

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Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).
Annalisa Botta, Sara Caldarola, Laura Vallo, Emanuela Bonifazi, Doriana Fruci

Biochim Biophys Acta· March 2006

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Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I.
Emanuela Bonifazi, Francesca Gullotta, Laura Vallo, Raniero Iraci, Anna Maria Nardone

Clin Chem· February 2006

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A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2.
Emanuela Bonifazi, Laura Vallo, Emiliano Giardina, Annalisa Botta, Giuseppe Novelli

Diagn Mol Pathol· September 2004

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CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease.
Piero Vavassori, Paola Borgiani, Livia Biancone, Maria Rosaria D'Apice, Giovanna Del Vecchio Blanco, Laura Vallo

Inflamm Bowel Dis· March 2004

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Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population.
Paola Borgiani, Laura Vallo, Maria Rosaria D'Apice, Emiliano Giardina, Sabina Pucci

Eur J Dermatol· March 2003

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