Publications by authors named "Silvana Tedeschi"

33Publications

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

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

Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes Insipidus.

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.

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.

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

Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.

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

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

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

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

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

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.

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