Publications by authors named "Luigi Citrigno"

18Publications

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

A 71-nucleotide deletion in the periaxin gene in an Italian patient with late-onset slowly progressive demyelinating CMT.

Eur J Neurol 2020 May 27. Epub 2020 May 27.

Institute for Biomedical Research and Innovation, National Research Council (CNR), Mangone, CS, Italy.

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http://dx.doi.org/10.1111/ene.14362DOI Listing
May 2020

ALS and CHARGE syndrome: a clinical and genetic study.

Acta Neurol Belg 2018 Dec 13;118(4):629-635. Epub 2018 Oct 13.

Institute of Neurological Sciences (ISN), National Research Council, C.da Burga, Mangone, CS, Italy.

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http://link.springer.com/10.1007/s13760-018-1029-2
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http://dx.doi.org/10.1007/s13760-018-1029-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244742PMC
December 2018

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.

Epilepsy Res 2014 Mar 18;108(3):597-9. Epub 2013 Nov 18.

Institute of Neurological Sciences, National Research Council, Cosenza 87050, Mangone, Italy; Institute of Neurology, University "Magna Graecia", Germaneto (CZ) 88100, Catanzaro, Italy. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S09201211130029
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http://dx.doi.org/10.1016/j.eplepsyres.2013.11.011DOI Listing
March 2014

Phenotypic heterogeneity in hereditary motor neuropathy type V: a new case report series.

Acta Neurol Belg 2012 Mar 9;112(1):57-64. Epub 2012 Feb 9.

Biochemistry and Molecular Biology Section, Department of Chemistry, University of Catania, Catania, Italy.

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http://dx.doi.org/10.1007/s13760-012-0042-0DOI Listing
March 2012

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

Gene symbol: MECP2. Disease: Rett syndrome.

Hum Genet 2008 Jun;123(5):555

Institute of Neurological Sciences, CNR, Localita` Burga, nd, 87050, Mangone (CS), Italy.

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June 2008

Gene symbol: NOTCH3. Disease: CADASIL.

Hum Genet 2008 Jun;123(5):555

Institute of Neurological Sciences, CNR, Localita` Burga, nd, 87050, Mangone (CS), Italy.

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June 2008

Gene symbol: NOTCH3. Disease: CADASIL.

Hum Genet 2008 Jun;123(5):554

Institute of Neurological Sciences, CNR, Località Burga, nd, 87050, Mangone (CS), Italy.

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June 2008