Viviana Caputo

Viviana Caputo

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Viviana Caputo

Viviana Caputo

Publications by authors named "Viviana Caputo"

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Intussusception After Roux-en-Y Gastric Bypass: Laparoscopic Management.

Obes Surg 2018 07;28(7):2145-2147

Department of Surgery, Bariatric and Metabolic Surgery Unit, Santa Maria Nuova Hospital, Piazza Santa Maria Nuova, 50122, Florence, Italy.

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http://dx.doi.org/10.1007/s11695-018-3265-1DOI Listing
July 2018

Biallelic mutations in early-onset, variably progressive neurodegeneration.

Neurology 2018 07 29;91(4):e319-e330. Epub 2018 Jun 29.

From the Genetics and Rare Diseases Research Division (V.M., G.C., T.R., M.D.N., A.C., F.P., R.C., M.T.), Ospedale Pediatrico Bambino Gesù; Department of Oncology and Molecular Medicine (E.F., S.M.) and Confocal Microscopy Unit (S.C.), Core Facilities, Istituto Superiore di Sanità, Rome, Italy; Center for Human Disease Modeling (Z.K., M.M.K., N.K.), Duke University School of Medicine, Durham, NC; Institutes of Neurology (G.P., S.S.) and Nuclear Medicine (D.D.G.), Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario A. Gemelli, Rome, Italy; Department of Genetics (H.G., N.M.), Faculty of Science, Shahid Chamran University of Ahvaz; Narges Medical Genetics and Prenatal Diagnosis Laboratory (H.G., N.M., A. Sedaghat, J.Z., G.R.S.), Kianpars, Ahvaz; Research and Clinical Center for Infertility (M.D.), Yazd Reproductive Sciences Institute, Medical Genetics Research Centre (M.D., M.Y.V.M.), and Department of Medical Genetics (M.Y.V.M.), Shahid Sadoughi University of Medical Sciences, Yazd, Iran; Department of Experimental Medicine (A.T., V.C.), Università "Sapienza," Rome, Italy; Genetics and Molecular Cell Sciences Research Centre (Y.J., R.M.), St. George's University of London, UK; Department of Paediatric Neurology (R.A.M.), Golestan Medical, Educational, and Research Center, and Department of Medical Genetics (G.R.S.), Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Iran; University of Exeter Medical School (A.R.J.), RILD, Royal Devon & Exeter Hospital, UK; and Department of Neurology (A. Sherafat), Kerman University of Medical Sciences, Iran.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000005869DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070386PMC
July 2018

Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes.

Eur J Paediatr Neurol 2017 May 19;21(3):475-484. Epub 2016 Dec 19.

University of Torino, Department of Medical Sciences, 10126, Turin, Italy; Città della Salute e della Scienza University Hospital, Medical Genetics Unit, Turin, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2016.12.005DOI Listing
May 2017

Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy.

Gene 2016 Feb 2;577(2):227-35. Epub 2015 Dec 2.

Medical Genetics, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, Circonvallazione Gianicolense, 87-00152 Rome, Italy.

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http://dx.doi.org/10.1016/j.gene.2015.11.048DOI Listing
February 2016

The emerging role of MicroRNA in schizophrenia.

CNS Neurol Disord Drug Targets 2015 ;14(2):208-21

Department of Experimental Medicine Sapienza University of Rome, Viale Regina Elena, 324, 00161 - Rome, Italy.

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November 2015

Mutations in PAX2 associate with adult-onset FSGS.

J Am Soc Nephrol 2014 Sep 27;25(9):1942-53. Epub 2014 Mar 27.

Division of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts;

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http://dx.doi.org/10.1681/ASN.2013070686DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147972PMC
September 2014

Novel SMAD4 mutation causing Myhre syndrome.

Am J Med Genet A 2014 Jul 8;164A(7):1835-40. Epub 2014 Apr 8.

Dipartimento di Medicina Sperimentale, Sapienza Università di Roma, Rome, Italy.

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http://dx.doi.org/10.1002/ajmg.a.36544DOI Listing
July 2014

Quantification of small non-coding RNAs allows an accurate comparison of miRNA expression profiles.

J Biomed Biotechnol 2009 1;2009:659028. Epub 2009 Sep 1.

Gene Expression and Microarrays Laboratory, Bambino Gesú Children's Hospital, P. za S. Onofrio 4, 00165 Rome, Italy.

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http://dx.doi.org/10.1155/2009/659028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735750PMC
November 2009

Insights into the interaction of sortilin with proneurotrophins: a computational approach.

Neuropeptides 2008 Apr 8;42(2):205-14. Epub 2008 Jan 8.

Dipartimento di Scienze Biochimiche A. Rossi Fanelli, Università di Roma La Sapienza, Piazzale Aldo Moro 5, Via degli Apuli 9, 00185 Rome, Italy.

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http://dx.doi.org/10.1016/j.npep.2007.11.004DOI Listing
April 2008

Mitochondrial import and enzymatic activity of PINK1 mutants associated to recessive parkinsonism.

Hum Mol Genet 2005 Nov 5;14(22):3477-92. Epub 2005 Oct 5.

Human Molecular Genetics Unit, Dibit-San Raffaele Scientific Institute, Milan, Italy.

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http://dx.doi.org/10.1093/hmg/ddi377DOI Listing
November 2005

A novel locus for autosomal dominant cone and cone-rod dystrophies maps to the 6p gene cluster of retinal dystrophies.

Invest Ophthalmol Vis Sci 2005 Oct;46(10):3539-44

Istituto di Ricovero e Cura a Carattere Scientifico Casa Sollievo della Sofferenza (IRCCS CSS), Mendel Institute, Rome, Italy.

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http://dx.doi.org/10.1167/iovs.05-0331DOI Listing
October 2005

Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.

Ann Neurol 2002 Jun;51(6):681-5

Neurogenetics, C.S.S. Mendel Institute, Viale Regina Margherita 261, I-00168 Rome, Italy.

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http://dx.doi.org/10.1002/ana.10204DOI Listing
June 2002