Publications by authors named "Arduino Carlo"

Claim this Profile
N
Next-Generation Sequencing Advances the Genetic Diagnosis of Cerebral Cavernous Malformation (CCM).
Valerio Benedetti, Rosalia Canzoneri, Andrea Perrelli, Carlo Arduino, Andrea Zonta

Antioxidants (Basel)· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations.
Stefano Paolacci, Raul Ettore Mattassi, Giuseppe Marceddu, Elena Manara, Alessandra Zulian, Carlo Arduino

J Clin Med· October 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hereditary pancreatitis in Paediatrics: the causative role of p.Leu104Pro mutation of cationic trypsinogen gene also in young subjects.
Ausilia Enea, Antonio Pizzol, Michele Pinon, Fabio Cisarò, Francesco Tandoi, Carlo Arduino

Gut· April 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Aberrant expression of aquaporin-3 in hereditary papulotranslucent acrokeratoderma and aquagenic palmoplantar keratoderma.
Laura Cristina Gironi, Enrico Colombo, Francesca Zottarelli, Andrea Guala, Carlo Arduino

Eur J Dermatol· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome.
Arianna Tucci, Luisa Ronzoni, Carlo Arduino, Paola Salmin, Susanna Esposito

BMC Med Genet· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NT5E mutations and arterial calcifications.
Cynthia St Hilaire, Shira G Ziegler, Thomas C Markello, Alfredo Brusco, Catherine Groden, Carlo Arduino

N Engl J Med· February 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia.
Alessandro Brussino, Claudio Graziano, Dario Giobbe, Marina Ferrone, Elisa Dragone, Carlo Arduino

Mov Disord· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A deletion 3' to the PAX6 gene in familial aniridia cases.
Angela Valentina D'Elia, Lucia Pellizzari, Dora Fabbro, Annalisa Pianta, Maria Teresa Divizia, Carlo Arduino

Mol Vis· July 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene.
Alessandro Saluto, Alessandro Brussino, Flora Tassone, Carlo Arduino, Claudia Cagnoli

J Mol Diagn· November 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Fcgamma receptor IIA genotype and susceptibility to P. aeruginosa infection in patients with cystic fibrosis.
Virginia De Rose, Carlo Arduino, Nazario Cappello, Rita Piana, Paola Salmin

Eur J Hum Genet· January 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Germline mutations in CFTR and PSTI genes in chronic pancreatitis patients.
Ezio Gaia, Paola Salacone, Monica Gallo, Gianni Gerbino Promis, Alfredo Brusco, Arduino Carlo

Dig Dis Sci· November 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Modifications of [3H]imipramine binding sites in platelets of chronic pain patients treated with mianserin.
Guido Magni, Francesca Andreoli, Carlo Arduino, Diego Arsie, Francesco Ceccherelli

Pain· September 1987

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis