Alessandro Ferraris

Alessandro Ferraris

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Alessandro Ferraris

Alessandro Ferraris

Publications by authors named "Alessandro Ferraris"

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35Publications

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The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiers.

J Hum Genet 2019 Aug 13;64(8):721-728. Epub 2019 May 13.

Medical Genetics Laboratory, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.

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http://dx.doi.org/10.1038/s10038-019-0598-0DOI Listing
August 2019

Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.

Eur J Med Genet 2019 Aug 14:103739. Epub 2019 Aug 14.

Medical Genetics Laboratory, Department of Molecular Medicine, Sapienza University, San Camillo-Forlanini Hospital, Rome, Italy.

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http://dx.doi.org/10.1016/j.ejmg.2019.103739DOI Listing
August 2019

Characterization of Two Novel Intronic Variants Affecting in -Related Disorders.

Genes (Basel) 2019 06 10;10(6). Epub 2019 Jun 10.

Division of Medical Genetics, Fondazione IRCCS-Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo FG, Italy.

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http://dx.doi.org/10.3390/genes10060442DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627396PMC
June 2019

From Design to Manufacture of a Carbon Fiber Monocoque for a Three-Wheeler Vehicle Prototype.

Materials (Basel) 2019 Jan 22;12(3). Epub 2019 Jan 22.

Department of Mechanical and Aerospace Engineering, Politecnico di Torino, 10129 Turin, Italy.

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http://dx.doi.org/10.3390/ma12030332DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384701PMC
January 2019

Nintendo Wii Fit for balance rehabilitation in patients with Parkinson's disease: A comparative study.

J Bodyw Mov Ther 2017 Jan 11;21(1):117-123. Epub 2016 Jun 11.

IRCCS Don Gnocchi Foundation, Milan, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.jbmt.2016.06.001DOI Listing
January 2017

Phenotypic variability of PINK1 expression: 12 Years' clinical follow-up of two Italian families.

Mov Disord 2014 Oct 27;29(12):1561-6. Epub 2014 Aug 27.

Institute of Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.

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http://dx.doi.org/10.1002/mds.25994DOI Listing
October 2014

Genetic testing for paediatric neurological disorders.

Lancet Neurol 2008 Dec;7(12):1113-26

Casa Sollievo della Sofferenza Hospital, Mendel Institute, Rome, Italy.

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http://dx.doi.org/10.1016/S1474-4422(08)70257-6DOI Listing
December 2008

CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing.

Clin Chem 2003 Oct;49(10):1675-9

Department of Medicine, Thomas Jefferson University, Jefferson Medical College, Philadelphia, PA 19104, USA.

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http://dx.doi.org/10.1373/49.10.1675DOI Listing
October 2003

Analysis of clinically relevant single-nucleotide polymorphisms by use of microelectronic array technology.

Clin Chem 2002 Dec;48(12):2124-30

Department of Pediatrics, The Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

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December 2002

Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss.

Hum Mutat 2002 Oct;20(4):312-20

Department of Pediatrics, The Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

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http://dx.doi.org/10.1002/humu.10127DOI Listing
October 2002