Publications by authors named "Alessandra Sironi"

7Publications

Molecular Etiology Disclosed by Array CGH in Patients With Silver-Russell Syndrome or Similar Phenotypes.

Authors:
Milena Crippa Maria Teresa Bonati Luciano Calzari Chiara Picinelli Cristina Gervasini Alessandra Sironi Ilaria Bestetti Sara Guzzetti Simonetta Bellone Angelo Selicorni Alessandro Mussa Andrea Riccio Giovanni Battista Ferrero Silvia Russo Lidia Larizza Palma Finelli

Front Genet 2019 15;10:955. Epub 2019 Oct 15.

Research Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, Milan, Italy.

View Article and Find Full Text PDF
October 2019

A Clinical and Radiographic Retrospective Study on 223 Anodized Surface Implants with a 5- to 17-Year Follow-up.

Authors:
Luca Ferrantino Francesco Tironi Stefano Pieroni Alessandra Sironi Massimo Simion

Int J Periodontics Restorative Dent 2019 Nov/Dec;39(6):799-807

View Article and Find Full Text PDF
October 2019

9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression.

Authors:
Maria Teresa Bonati Chiara Castronovo Alessandra Sironi Dario Zimbalatti Ilaria Bestetti Milena Crippa Antonio Novelli Sara Loddo Maria Lisa Dentici Juliet Taylor Françoise Devillard Lidia Larizza Palma Finelli

Neurogenetics 2019 08 17;20(3):145-154. Epub 2019 Jun 17.

Research Lab of Medical Cytogenetics and Molecular Genetics, Istituto Auxologico Italiano, IRCCS, 20145, Milan, Italy.

View Article and Find Full Text PDF
August 2019

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features.

Authors:
Valentina Cirello Valentina Giorgini Chiara Castronovo Susan Marelli Ester Mainini Alessandra Sironi Maria Paola Recalcati Marco Pessina Daniela Giardino Lidia Larizza Luca Persani Palma Finelli Silvia Russo Laura Fugazzola

Front Genet 2018 30;9:600. Epub 2018 Nov 30.

Division of Endocrine and Metabolic Diseases, Laboratory of Endocrine and Metabolic Research, IRCCS Istituto Auxologico Italiano, Milan, Italy.

View Article and Find Full Text PDF
November 2018

13q mosaic deletion including associated to mild phenotype and no cancer outcome - case report and review of the literature.

Authors:
Ilaria Bestetti Alessandra Sironi Ilaria Catusi Milena Mariani Daniela Giardino Siranoush Manoukian Donatella Milani Lidia Larizza Chiara Castronovo Palma Finelli

Mol Cytogenet 2018 19;11:53. Epub 2018 Sep 19.

1Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, via Ariosto 13, 20145 Milan, Italy.

View Article and Find Full Text PDF
September 2018

iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability.

Authors:
Valentina Alari Silvia Russo Benedetta Terragni Paola Francesca Ajmone Alessandra Sironi Ilaria Catusi Luciano Calzari Daniela Concolino Rosa Marotta Donatella Milani Daniela Giardino Massimo Mantegazza Cristina Gervasini Palma Finelli Lidia Larizza

Stem Cell Res 2018 07 30;30:130-140. Epub 2018 May 30.

Laboratory of Medical Cytogenetics and Molecular Genetics, Centro di Ricerche e Tecnologie Biomediche, IRCCS Istituto Auxologico Italiano, 20145 Milano, Italy. Electronic address:

View Article and Find Full Text PDF
July 2018

Rothmund-Thomson Syndrome: Insights from New Patients on the Genetic Variability Underpinning Clinical Presentation and Cancer Outcome.

Authors:
Elisa A Colombo Andrea Locatelli Laura Cubells Sánchez Sara Romeo Nursel H Elcioglu Isabelle Maystadt Altea Esteve Martínez Alessandra Sironi Laura Fontana Palma Finelli Cristina Gervasini Vanna Pecile Lidia Larizza

Int J Mol Sci 2018 Apr 6;19(4). Epub 2018 Apr 6.

Laboratory of Medical Cytogenetics and Molecular Genetics, IRCCS Istituto Auxologico Italiano, 20149 Milan, Italy.

View Article and Find Full Text PDF
April 2018