Publications by authors named "Francesca Cavalcanti"

11Publications

The Mitochondrial Dysfunction Hypothesis in Autism Spectrum Disorders: Current Status and Future Perspectives.

Int J Mol Sci 2020 Aug 12;21(16). Epub 2020 Aug 12.

Institute for Biomedical Research and Innovation, National Research Council, IRIB-CNR, 87050 Mangone CS, Italy.

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http://dx.doi.org/10.3390/ijms21165785DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461038PMC
August 2020

Large Interruptions of GAA Repeat Expansion Mutations in Friedreich Ataxia Are Very Rare.

Front Cell Neurosci 2018 21;12:443. Epub 2018 Nov 21.

Ataxia Research Group, Division of Biosciences, Department of Life Sciences, College of Health and Life Sciences, Brunel University London, Uxbridge, United Kingdom.

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http://dx.doi.org/10.3389/fncel.2018.00443DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258883PMC
November 2018

: 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

Expanding the global prevalence of spinocerebellar ataxia type 42.

Neurol Genet 2018 Jun 5;4(3):e232. Epub 2018 Apr 5.

Department of Neurology (K.J.N., M.A., S.P., G.C., B.L.F.), Program in Neurogenetics, David Geffen School of Medicine, University of California, Los Angeles; Department of Medical Genetics (L.E.P., J.E.B.), Vanderbilt University Medical Center, Nashville, TN; Department of Psychiatry and Biobehavioral Sciences (J.A.C., G.C.), University of California, Los Angeles, CA; Institute of Neurological Sciences (F.C., S.C.), Italian National Research Council, Mangone, Italy; Department of Neurology (A.B.N., M.D.G.), UCSF Memory and Aging Center, University of California, San Francisco; Sackler Faculty of Medicine (S.H.), Tel-Aviv University, Israel; Italian College of General Practitioners and Primary Care (D.I.), Department of Clinical and Experimental Medicine (A.L.), University of Messina, Italy; and the Department of Human Genetics (B.L.F.), David Geffen School of Medicine, University of California, Los Angeles.

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http://dx.doi.org/10.1212/NXG.0000000000000232DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886831PMC
June 2018

Splicing: is there an alternative contribution to Parkinson's disease?

Neurogenetics 2015 Oct 16;16(4):245-63. Epub 2015 May 16.

Institute of Neurological Sciences, Italian National Research Council, Via Paolo Gaifami 18, 95125, Catania, Sicily, Italy.

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http://dx.doi.org/10.1007/s10048-015-0449-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573652PMC
October 2015

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