Enrico Farnetti

Enrico Farnetti

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Enrico Farnetti

Enrico Farnetti

Publications by authors named "Enrico Farnetti"

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Three Reportedly Unrelated Families With Liddle Syndrome Inherited From a Common Ancestor.

Hypertension 2018 02 11;71(2):273-279. Epub 2017 Dec 11.

From the Department of Biology (L.P.) and Endocrinology Unit, Department of Medicine (F.M.), University of Padova, Italy; Estonian Biocentre, Tartu (L.P.); Research Department of Genetics, Evolution and Environment, University College London, United Kingdom (Y.D., M.G.T.); Department of Biological Geological and Environmental Sciences (M.S., S.D.F., D.L.) and Department of Experimental, Diagnostic and Specialty Medicine (P.G.), University of Bologna, Italy; IRCCS Centro Cardiologico Monzino, Milano, Italy (M.R.); Department of Oncology and Advanced Technologies, Laboratory of Molecular Biology (E.F., B.C.) and Department of Internal Medicine (E.R.), IRCCS Santa Maria Nuova Hospital, Reggio Emilia, Italy; Department of Endocrinology and Metabolic Diseases, San Raffaele Scientific Institute, Milano, Italy (A.C.); and Department of Molecular Medicine, University of Pavia, Italy (F.N., O.Z.).

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http://dx.doi.org/10.1161/HYPERTENSIONAHA.117.10491DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767121PMC
February 2018

Peptide Receptor Radionuclide Therapy-Induced Gitelman-like Syndrome.

Am J Kidney Dis 2017 Nov 21;70(5):725-728. Epub 2017 Jul 21.

Emergency Department, IRCCS-Arcispedale Santa Maria Nuova, Reggio Emilia, Italy.

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http://dx.doi.org/10.1053/j.ajkd.2017.05.024DOI Listing
November 2017

Transformation of IGHV4-34+ hairy cell leukaemia-variant with U2AF1 mutation into a clonally-related high grade B-cell lymphoma responding to immunochemotherapy.

Br J Haematol 2016 05 25;173(3):491-5. Epub 2015 Aug 25.

Institute of Haematology and C.R.E.O. (Centro di Ricerche Onco-Ematologiche), Ospedale S. Maria della Misericordia and University of Perugia, Perugia, Italy.

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http://doi.wiley.com/10.1111/bjh.13627
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http://dx.doi.org/10.1111/bjh.13627DOI Listing
May 2016

Polymorphisms in cyclooxygenase-2 gene in endometrial cancer patients.

Tumour Biol 2015 Sep 22;36(10):7423-30. Epub 2015 Apr 22.

Unit of Obstetrics and Gynaecology, Arcispedale Santa Maria Nuova-IRCCS, Reggio Emilia, Italy.

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http://dx.doi.org/10.1007/s13277-015-3424-0DOI Listing
September 2015

CC chemokine receptor 5 polymorphism in Italian patients with giant cell arteritis.

Mod Rheumatol 2013 Sep 23;23(5):851-5. Epub 2012 Sep 23.

Rheumatology Unit, Department of Internal Medicine, Azienda Ospedaliera Arcispedale S Maria Nuova, Istituto di Ricovero e Cura a Carattere Scientifico, Viale Risorgimento n 80, 42100, Reggio Emilia, Italy.

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http://dx.doi.org/10.1007/s10165-012-0751-5DOI Listing
September 2013

Fluoropyrimidine toxicity in patients with dihydropyrimidine dehydrogenase splice site variant: the need for further revision of dose and schedule.

Intern Emerg Med 2013 Aug 13;8(5):417-23. Epub 2013 Apr 13.

Department of Medical Oncology, Azienda Ospedaliera ASMN, IRCCS, Reggio Emilia, Italy.

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http://dx.doi.org/10.1007/s11739-013-0936-8DOI Listing
August 2013

Very early onset and severe complicated phenotype caused by a new spastic paraplegia 3A gene mutation.

J Child Neurol 2012 Oct 28;27(10):1348-50. Epub 2012 Feb 28.

Pediatric Neurology Unit, Arcispedale Santa Maria Nuova, Viale Risorgimento 80, Reggio Emilia, Italy.

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http://journals.sagepub.com/doi/10.1177/0883073811435245
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http://dx.doi.org/10.1177/0883073811435245DOI Listing
October 2012

Haptoglobin phenotype and epithelial ovarian cancer.

Anticancer Res 2012 Oct;32(10):4353-8

Department of Obstetrics and Gynecology, Arcispedale Santa Maria Nuova di Reggio Emilia, IRCCS, Viale Risorgimento 80, Reggio Emilia, Italy.

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October 2012

A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome.

Am J Hypertens 2011 Aug 28;24(8):930-5. Epub 2011 Apr 28.

Second Unit of Internal Medicine, Department of Internal Medicine, Santa Maria Nuova Hospital, Reggio Emilia, Italy.

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http://dx.doi.org/10.1038/ajh.2011.76DOI Listing
August 2011

Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.

Brain Dev 2010 Aug 6;32(7):592-4. Epub 2009 Sep 6.

Child Neurology Unit, Arcispedale Santa Maria Nuova, Reggio Emilia, Italy.

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http://dx.doi.org/10.1016/j.braindev.2009.08.003DOI Listing
August 2010

Interleukin-6 promoter polymorphism at position -174 in giant cell arteritis.

J Rheumatol 2005 Nov;32(11):2173-7

Unità Operativa di Reumatologia, Laboratorio di Biologia Molecolare, Arcispedale S. Maria Nuova, Reggio Emilia, Italy.

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November 2005

Vascular endothelial growth factor gene polymorphisms in giant cell arteritis.

J Rheumatol 2003 Oct;30(10):2160-4

Servizio di Reumatologia and Laboratorio di Biologia Molecolare, Azienda Ospedaliera Arcispedale S. Maria Nuova, Viale Umberto 1 N50, 42100 Reggio Emilia, Italy.

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October 2003