Emanuela Castiglioni

Emanuela Castiglioni

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Emanuela Castiglioni

Emanuela Castiglioni

Publications by authors named "Emanuela Castiglioni"

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Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study.

Clin Chim Acta 2015 Dec 8;451(Pt A):39-45. Epub 2015 Jan 8.

Unit of Genomics for Diagnosis of Human Pathologies, Division of Genetics and Cell Biology, IRCCS Ospedale San Raffaele, Milano, Italy.

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http://dx.doi.org/10.1016/j.cca.2015.01.001DOI Listing
December 2015

Genetic susceptibility to neonatal lung diseases.

Acta Biomed 2012 ;83 Suppl 1:10-4

Unità di Genomica per la Diagnostica delle Patologie Umane, Centro di Genomica Traslazionale e Bioinformatica, Istituto Scientifico San Raffaele, Milano.

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November 2012

Genetic predisposing factors to bronchopulmonary dysplasia: preliminary data from a multicentre study.

J Matern Fetal Neonatal Med 2012 Oct;25 Suppl 4:127-30

Genomic Unit for Diagnosis of Human Pathologies, Center for Translational Genomics and Bioinformatics, Ospedale San Raffaele, Milan, Italy.

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http://dx.doi.org/10.3109/14767058.2012.714995DOI Listing
October 2012

Sequence variations in mitochondrial ferritin: distribution in healthy controls and different types of patients.

Genet Test Mol Biomarkers 2010 Dec 12;14(6):793-6. Epub 2010 Oct 12.

Genomic Unit for the Diagnosis of Human Pathologies, Center for Genomics, Bioinformatics, and Biostatistics, San Raffaele Scientific Institute, Milan, Italy.

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http://dx.doi.org/10.1089/gtmb.2010.0076DOI Listing
December 2010

High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene.

Clin Chem Lab Med 2010 Oct 27;48(10):1415-8. Epub 2010 Jun 27.

San Raffaele Scientific Institute, Center for Genomics, Bioinformatics and Biostatistics, Genomic Unit for the Diagnosis of Human Pathologies, Milan, Italy.

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http://dx.doi.org/10.1515/CCLM.2010.281DOI Listing
October 2010

Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders.

Parkinsons Dis 2010 Oct 17;2011:827693. Epub 2010 Oct 17.

Genomic Unit for the Diagnosis of Human Pathologies, Center for Genomics, Bioinformatics and Biostatistics, San Raffaele Scientific Institute, 20132 Milan, Italy.

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http://dx.doi.org/10.4061/2011/827693DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2957853PMC
October 2010