Publications by authors named "Silvana Tedeschi"

33Publications

Genetic and molecular evidence for complement dysregulation in patients with HELLP syndrome.

Authors:
Mario Bazzan Tullia Todros Silvana Tedeschi Gianluigi Ardissino Simona Cardaropoli Stefania Stella Barbara Montaruli Cristiana Marchese Dario Roccatello Massimo Cugno

Thromb Res 2020 12 27;196:167-174. Epub 2020 Aug 27.

Internal Medicine, Department of Pathophysiology and Transplantation, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Via Pace 9, 20122 Milan, Italy. Electronic address:

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December 2020

Functional Study of Novel Bartter's Syndrome Mutations in ClC-Kb and Rescue by the Accessory Subunit Barttin Toward Personalized Medicine.

Authors:
Dalila Sahbani Bice Strumbo Silvana Tedeschi Elena Conte Giulia Maria Camerino Elisa Benetti Giovanni Montini Gabriella Aceto Giuseppe Procino Paola Imbrici Antonella Liantonio

Front Pharmacol 2020 17;11:327. Epub 2020 Mar 17.

Department of Pharmacy-Drug Sciences, University of Bari "Aldo Moro", Bari, Italy.

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March 2020

The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.

Authors:
Marcella Neri Rachele Rossi Cecilia Trabanelli Antonio Mauro Rita Selvatici Maria Sofia Falzarano Noemi Spedicato Alice Margutti Paola Rimessi Fernanda Fortunato Marina Fabris Francesca Gualandi Giacomo Comi Silvana Tedeschi Manuela Seia Chiara Fiorillo Monica Traverso Claudio Bruno Emiliano Giardina Maria Rosaria Piemontese Giuseppe Merla Milena Cau Monica Marica Carmela Scuderi Eugenia Borgione Alessandra Tessa Guia Astrea Filippo Maria Santorelli Luciano Merlini Marina Mora Pia Bernasconi Sara Gibertini Valeria Sansone Tiziana Mongini Angela Berardinelli Antonella Pini Rocco Liguori Massimiliano Filosto Sonia Messina Gianluca Vita Antonio Toscano Giuseppe Vita Marika Pane Serenella Servidei Elena Pegoraro Luca Bello Lorena Travaglini Enrico Bertini Adele D'Amico Manuela Ergoli Luisa Politano Annalaura Torella Vincenzo Nigro Eugenio Mercuri Alessandra Ferlini

Front Genet 2020 3;11:131. Epub 2020 Mar 3.

Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.

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March 2020

Haploidentical Hematopoietic Stem Cell Transplant Complicated by Atypical Hemolytic Uremic Syndrome and Kidney Transplant From the Same Donor With No Immunosuppression but C5 Inhibition.

Authors:
Gianluigi Ardissino Donata Cresseri Fabio Giglio Francesco Onida Francesco Iannuzzella Francesca Tel Antenore Giussani Piergiorgio Messa Selena Longhi Daniele Vincenti Silvana Tedeschi Massimo Cugno Fabio Ciceri

Transplantation 2019 02;103(2):e48-e51

Hematology and Bone Marrow Transplantation Unit, IRCCS S. Raffaele Scientific Institution, Milan, Italy.

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February 2019

Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes Insipidus.

Authors:
Gianluca Vergine Elena Fabbri Annalisa Pedini Silvana Tedeschi Niccolò Borsa

Case Rep Pediatr 2018 21;2018:9175271. Epub 2018 Feb 21.

Medical Genetics Laboratory, Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Milan, Italy.

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February 2018

Response.

Authors:
Gianluigi Ardissino Silvana Tedeschi Marco Zecca Silvia Berra Giacomo Colussi Fabio Giglio Elisabetta Terruzzi Massimo Cugno

Biol Blood Marrow Transplant 2017 11 15;23(11):2014-2015. Epub 2017 Aug 15.

Medicina Interna, Dipartimento di Fisiopatologia Medico Chirurgica, Università degli Studi di Milano, IRCCS Fondazione Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.

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November 2017

Acquired Complement Regulatory Gene Mutations and Hematopoietic Stem Cell Transplant-Related Thrombotic Microangiopathy.

Authors:
Gianluigi Ardissino Stefania Salardi Silvia Berra Giacomo Colussi Massimo Cugno Marco Zecca Fabio Giglio Jacopo Peccatori Elisa Diral Francesca Tel Alberto Clivio Silvana Tedeschi

Biol Blood Marrow Transplant 2017 Sep 15;23(9):1580-1582. Epub 2017 May 15.

Laboratory of Medical Genetics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

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September 2017

Early Volume Expansion and Outcomes of Hemolytic Uremic Syndrome.

Authors:
Gianluigi Ardissino Francesca Tel Ilaria Possenti Sara Testa Dario Consonni Fabio Paglialonga Stefania Salardi Nicolò Borsa-Ghiringhelli Patrizia Salice Silvana Tedeschi Pierangela Castorina Rosaria Maria Colombo Milena Arghittu Laura Daprai Alice Monzani Rosangela Tozzoli Maurizio Brigotti Erminio Torresani

Pediatrics 2016 Jan 7;137(1). Epub 2015 Dec 7.

Unit of Microbiology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy;

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January 2016

Epidemiology of haemolytic uremic syndrome in children. Data from the North Italian HUS network.

Authors:
Gianluigi Ardissino Stefania Salardi Elisa Colombo Sara Testa Nicolò Borsa-Ghiringhelli Fabio Paglialonga Valentina Paracchini Francesca Tel Ilaria Possenti Mirco Belingheri Cristina Felice Civitillo Stefano Sardini Rossella Ceruti Carlo Baldioli Paola Tommasi Luciana Parola Fiorella Russo Silvana Tedeschi

Eur J Pediatr 2016 Apr 24;175(4):465-73. Epub 2015 Oct 24.

Center for Prevention, Control and Management of Hemolytic Uremic Syndrome, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

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April 2016

Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.

Authors:
Samuele Corbetta Francesca Raimondo Silvana Tedeschi Marie-Louise Syrèn Paola Rebora Andrea Savoia Lorenza Baldi Alberto Bettinelli Marina Pitto

Nephrol Dial Transplant 2015 Apr 23;30(4):621-30. Epub 2014 Nov 23.

Department of Health Sciences, University of Milano-Bicocca, Monza, Italy.

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April 2015

Hemoconcentration: a major risk factor for neurological involvement in hemolytic uremic syndrome.

Authors:
Gianluigi Ardissino Valeria Daccò Sara Testa Cristina Felice Civitillo Francesca Tel Ilaria Possenti Mirco Belingheri Pierangela Castorina Nicolò Bolsa-Ghiringhelli Silvana Tedeschi Fabio Paglialonga Stefania Salardi Dario Consonni Elena Zoia Patrizia Salice Giovanna Chidini

Pediatr Nephrol 2015 Feb 23;30(2):345-52. Epub 2014 Aug 23.

Center for HUS Control, Prevention and Management, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Commenda 9, 20122, Milan, Italy,

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February 2015

Phosphate homeostasis in Bartter syndrome: a case-control study.

Authors:
Alberto Bettinelli Cristina Viganò Maria Cristina Provero Francesco Barretta Alessandra Albisetti Silvana Tedeschi Barbara Scicchitano Mario G Bianchetti

Pediatr Nephrol 2014 Nov 6;29(11):2133-8. Epub 2014 Jun 6.

Division of Pediatrics, San Leopoldo Mandic Hospital, Merate, Lecco, Italy.

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November 2014

Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidus.

Authors:
Milena Brugnara Rossella Gaudino Silvana Tedeschi Marie-Louise Syrèn Silverio Perrotta Evelina Maines Marco Zaffanello

J Pediatr Endocrinol Metab 2014 Sep;27(9-10):971-5

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September 2014

Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 cases.

Authors:
Gianluigi Ardissino Sara Testa Ilaria Possenti Francesca Tel Fabio Paglialonga Stefania Salardi Silvana Tedeschi Mirco Belingheri Massimo Cugno

Am J Kidney Dis 2014 Oct 19;64(4):633-7. Epub 2014 Mar 19.

Center for HUS Prevention, Control and Management, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.

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October 2014

Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype.

Authors:
Simona Brioschi Francesca Gualandi Chiara Scotton Annarita Armaroli Matteo Bovolenta Maria S Falzarano Patrizia Sabatelli Rita Selvatici Adele D'Amico Marika Pane Giulia Ricci Gabriele Siciliano Silvana Tedeschi Antonella Pini Liliana Vercelli Domenico De Grandis Eugenio Mercuri Enrico Bertini Luciano Merlini Tiziana Mongini Alessandra Ferlini

BMC Med Genet 2012 Aug 16;13:73. Epub 2012 Aug 16.

Section of Medical Genetics, Department of Experimental and Diagnostic Medicine, University of Ferrara, Ferrara, Italy.

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August 2012

The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndrome.

Authors:
Francesca Crovetto Nicolò Borsa Barbara Acaia Carla Nishimura Kathy Frees Richard J H Smith Flora Peyvandi Roberta Palla Massimo Cugno Silvana Tedeschi Pierangela Castorina Edgardo Somigliana Gianluigi Ardissino Luigi Fedele

J Matern Fetal Neonatal Med 2012 Nov 7;25(11):2322-5. Epub 2012 Jun 7.

Department Obstet-Gynecol, Fondazione Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.

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November 2012

Diabetic ketoacidosis complicated with previously unknown Gitelman syndrome in a Tunisian child.

Authors:
Martina Biagioni Marco Marigliano Antonio Iannilli Annamaria Cester Simona Gatti Irene D'Alba Silvana Tedeschi Marie-Louise Syren Valentino Cherubini

Diabetes Care 2011 Jun;34(6):e107

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June 2011

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.

Authors:
Francesca Magri Alessandra Govoni Maria Grazia D'Angelo Roberto Del Bo Serena Ghezzi Gandossini Sandra Anna Carla Turconi Monica Sciacco Patrizia Ciscato Andreina Bordoni Silvana Tedeschi Francesco Fortunato Valeria Lucchini Sara Bonato Costanza Lamperti Domenico Coviello Yvan Torrente Stefania Corti Maurizio Moggio Nereo Bresolin Giacomo Pietro Comi

J Neurol 2011 Sep 12;258(9):1610-23. Epub 2011 Mar 12.

Department of Neurological Sciences, Dino Ferrari Centre, University of Milan, I.R.C.C.S. Foundation Ca' Granda, Ospedale Maggiore Policlinico, Padiglione Ponti, Via Francesco Sforza 35, 20122 Milan, Italy.

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September 2011

Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.

Authors:
Francesca Magri Roberto Del Bo Maria G D'Angelo Alessandra Govoni Serena Ghezzi Sandra Gandossini Monica Sciacco Patrizia Ciscato Andreina Bordoni Silvana Tedeschi Francesco Fortunato Valeria Lucchini Matteo Cereda Stefania Corti Maurizio Moggio Nereo Bresolin Giacomo P Comi

BMC Med Genet 2011 Mar 11;12:37. Epub 2011 Mar 11.

Dino Ferrari Centre, Department of Neurological Sciences, University of Milan, IRCCS Foundation Cà Granda, Ospedale Maggiore Policlinico, Milan, Italy.

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March 2011

The mutation c.1196_1202dup7bp (p.Ser402X) in the SLC12A3 gene clusters in Italian Gitelman syndrome patients and reflects the presence of a common ancestor.

Authors:
Marie-Louise Syrén Nicolò Borsa Ghiringhelli Alberto Bettinelli Giacomo Colussi Rosa Vargas-Poussou Fabiana Tammaro Domenico A Coviello Silvana Tedeschi

Nephrol Dial Transplant 2011 Feb 30;26(2):557-61. Epub 2010 Jul 30.

Dipartimento di Scienze Materno-Infantili, Universita degli Studi di Milano, Laboratorio di Genetica Medica, Fondazione IRCCS Ca’ Granda-Ospedale Maggiore Policlinico, Milan, Italy.

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February 2011