Elena Panzeri

Elena Panzeri

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Elena Panzeri

Elena Panzeri

Publications by authors named "Elena Panzeri"

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21Publications

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Naringenin Ameliorates ReepA Hereditary Spastic Paraplegia-Linked Phenotypes.

Front Neurosci 2019 19;13:1202. Epub 2019 Nov 19.

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.

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http://dx.doi.org/10.3389/fnins.2019.01202DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6877660PMC
November 2019

Epilepsy in Tubulinopathy: Personal Series and Literature Review.

Cells 2019 07 2;8(7). Epub 2019 Jul 2.

Neuropsychiatry and Neurorehabilitation Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, 23842 Lecco, Italy.

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http://dx.doi.org/10.3390/cells8070669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678821PMC
July 2019

Antipsychotics Promote Metabolic Disorders Disrupting Cellular Lipid Metabolism and Trafficking.

Trends Endocrinol Metab 2019 03 1;30(3):189-210. Epub 2019 Feb 1.

Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini (LC), 23842, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.tem.2019.01.003DOI Listing
March 2019

and Variants in a Family With Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis.

Front Neurol 2018 7;9:1078. Epub 2018 Dec 7.

Laboratory of Molecular Biology, Scientific Institute IRCCS E. Medea, Lecco, Italy.

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http://dx.doi.org/10.3389/fneur.2018.01078DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293196PMC
December 2018

Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.

J Neurol 2017 Sep 27;264(9):2021-2023. Epub 2017 Jul 27.

Laboratory of Molecular Biology, Scientific Institute IRCCS E. Medea, Bosisio Parini, Lecco, Italy.

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http://dx.doi.org/10.1007/s00415-017-8558-0DOI Listing
September 2017

Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis.

J Neurol 2015 Dec 26;262(12):2684-90. Epub 2015 Sep 26.

Laboratory of Molecular Biology, Scientific Institute IRCCS E. Medea, Via D. L. Monza 20, 23842, Bosisio Parini, Lecco, Italy.

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http://dx.doi.org/10.1007/s00415-015-7899-9DOI Listing
December 2015

A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype.

Neuroreport 2015 Mar;26(5):254-7

aNeuropsychiatry and Neurorehabilitation Unit bLaboratory of Molecular Biology cNeuroimaging Unit, Scientific Institute, IRCCS Eugenio Medea, Lecco dDepartment of Pediatrics, San Gerardo Hospital, Monza, University of Milano Bicocca, Milano, Italy.

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http://dx.doi.org/10.1097/WNR.0000000000000337DOI Listing
March 2015

Chromosomal imbalances in human bladder urothelial carcinoma: similarities and differences between biopsy samples and cancer stem-like cells.

BMC Cancer 2014 Sep 1;14:646. Epub 2014 Sep 1.

Department of Surgery and Translational Medicine, University of Milan-Bicocca, via Cadore 48, 20052 Monza, Italy.

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http://dx.doi.org/10.1186/1471-2407-14-646DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162911PMC
September 2014

Mutations in MAPT give rise to aneuploidy in animal models of tauopathy.

Neurogenetics 2014 Mar 12;15(1):31-40. Epub 2013 Nov 12.

Division of Neurology V and Neuropathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy,

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http://dx.doi.org/10.1007/s10048-013-0380-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968519PMC
March 2014

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis.

J Neurol 2014 Feb 13;261(2):373-81. Epub 2013 Dec 13.

Laboratory of Molecular Biology, Scientific Institute IRCCS Eugenio Medea, Via D. L. Monza 20, Bosisio Parini, 23842, Lecco, Italy.

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http://dx.doi.org/10.1007/s00415-013-7206-6DOI Listing
February 2014

Mutations in MAPT gene cause chromosome instability and introduce copy number variations widely in the genome.

J Alzheimers Dis 2013 ;33(4):969-82

Division of Neurology V and Neuropathology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy.

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http://dx.doi.org/10.3233/JAD-2012-121633DOI Listing
October 2013

DNA copy number alterations and PPARG amplification in a patient with multifocal bladder urothelial carcinoma.

BMC Res Notes 2012 Oct 31;5:607. Epub 2012 Oct 31.

Department of Neuroscience and Biomedical Technologies, University of Milan-Bicocca, Monza, Italy.

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http://dx.doi.org/10.1186/1756-0500-5-607DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598781PMC
October 2012

Cytogenetics of premature ovarian failure: an investigation on 269 affected women.

J Biomed Biotechnol 2011 17;2011:370195. Epub 2011 Jan 17.

Dipartimento di Neuroscienze e Tecnologie Biomediche, Università degli Studi di Milano-Bicocca, Via Cadore 48, 20900 Monza, Italy.

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http://dx.doi.org/10.1155/2011/370195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026995PMC
June 2011

Biological heterogeneity of putative bladder cancer stem-like cell populations from human bladder transitional cell carcinoma samples.

Cancer Sci 2010 Feb 27;101(2):416-24. Epub 2009 Oct 27.

Dipartimento di Neuroscienze e Tecnologie Biomediche, Università degli Studi di Milano-Bicocca, Monza, Italy.

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http://dx.doi.org/10.1111/j.1349-7006.2009.01414.xDOI Listing
February 2010