Publications by authors named "Alessandra Patitucci"

28Publications

A review of the antimicrobial potential of herbal drugs used in popular Italian medicine (1850s-1950s) to treat bacterial skin diseases.

J Ethnopharmacol 2020 Mar 29;250:112443. Epub 2019 Nov 29.

Institute for Agricultural and Forest Systems in the Mediterranean, National Research Council, Via Cavour 4-6, 87036, Rende, CS, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.jep.2019.112443DOI Listing
March 2020

: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders.

Curr Genomics 2018 Sep;19(6):431-443

1Institute of Neurological Sciences, National Research Council, Via Paolo Gaifami 18, 95125, Catania, Italy; 2Institute of Neurological Sciences, National Research Council, 87050, Mangone, Cosenza, Italy; 3Department of Biomedical and Biotechnological Sciences, Section of Human Anatomy and Histology, University of Catania, Catania, Italy; 4Unit of Rare Diseases of the Nervous System in Childhood, Department of Clinical and Experimental Medicine, Section of Pediatrics and Child Neuropsychiatry, University of Catania, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.

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http://www.eurekaselect.com/160974/article
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http://dx.doi.org/10.2174/1389202919666180404105451DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128384PMC
September 2018

A rare association between multiple sclerosis and Charcot-Marie-Tooth type 1B.

Brain Behav 2016 12 25;6(12):e00580. Epub 2016 Sep 25.

Department of Basic Medical Sciences, Neurosciences and Sense Organs University of Bari Bari Italy.

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http://dx.doi.org/10.1002/brb3.580DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167010PMC
December 2016

Normal immunofluorescence pattern of skin basement membranes in a family with porencephaly due to COL4A1 G749S mutation.

Neurol Sci 2016 Mar 19;37(3):459-63. Epub 2015 Dec 19.

Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy.

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http://dx.doi.org/10.1007/s10072-015-2435-3DOI Listing
March 2016

A novel NF1 gene mutation in an Italian family with neurofibromatosis type 1.

Childs Nerv Syst 2011 Apr 7;27(4):635-8. Epub 2010 Oct 7.

Institute of Neurological Science (ISN), National Research Council (CNR), Piano Lago di Mangone, Cosenza, Italy.

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http://dx.doi.org/10.1007/s00381-010-1282-zDOI Listing
April 2011

An axon regeneration signature in a Charcot-Marie-Tooth disease type 2 patient.

J Neurogenet 2009 ;23(3):324-8

Institute of Neurological Sciences, National Research Council, Mangone, Cosenza, Italy.

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http://dx.doi.org/10.1080/01677060802447585DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716698PMC
December 2011

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.

Brain Dev 2008 Apr 4;30(4):291-4. Epub 2007 Sep 4.

Unit of Neurometabolic Disease, Department of Neurological and Behavioural Sciences, University of Siena, Italy.

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http://dx.doi.org/10.1016/j.braindev.2007.07.010DOI Listing
April 2008

Putative role of specific JAG1 gene exons in modulating clinical features in patients with leukoencephalopathy.

Neurosci Lett 2007 May 1;418(1):1-3. Epub 2007 Mar 1.

Institute of Neurological Sciences, National Research Council, 87050 Mangone, Cosenza, Italy.

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http://dx.doi.org/10.1016/j.neulet.2007.02.059DOI Listing
May 2007