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Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies?

PPAR Research, 2015-01, Vol.2015, p.415149-10

2015

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Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes

International journal of molecular sciences, 2016-07, Vol.17 (7), p.1008

2016

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Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures

PloS one, 2012-08, Vol.7 (8), p.e43799-e43799

2012

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The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

Orphanet journal of rare diseases, 2013-01, Vol.8 (1), p.16-16, Article 16

2013

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Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration

Molecular therapy, 2010-03, Vol.18 (3), p.643-650

2010

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New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma

Oncotarget, 2015-05, Vol.6 (13), p.11242-11251

2015

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Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

Investigative ophthalmology & visual science, 2007-09, Vol.48 (9), p.4284-4290

2007

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A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

Investigative ophthalmology & visual science, 2009-04, Vol.50 (4), p.1864-1872

2009

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Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy

Investigative ophthalmology & visual science, 2011-07, Vol.52 (8), p.5618-5624

2011

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Molecular epidemiology of Usher syndrome in Italy

Molecular vision, 2011, Vol.17, p.1662-1668

2011

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Identification and expression analysis of novel Jakmip1 transcripts

Gene, 2007-11, Vol.402 (1), p.1-8

2007

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Identification and characterisation of the retinitis pigmentosa 1-like1 gene ( ): a novel candidate for retinal degenerations

European journal of human genetics : EJHG, 2003-02, Vol.11 (2), p.155-162

2003

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Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Biochemical and biophysical research communications, 2003-08, Vol.308 (3), p.414-421

2003

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Identification and characterisation of the retinitis pigmentosa 1-likel gene (RP1l1): a novel candidate for retinal degenerations

European journal of human genetics : EJHG, 2003, Vol.11 (2), p.155-162

2003

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Imaging of adrenal tumors using FDG PET: comparison of benign and malignant lesions

American journal of roentgenology (1976), 1999-07, Vol.173 (1), p.25

1999

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Pharmacogenomics of Drug Response in Type 2 Diabetes: Toward the Definition of Tailored Therapies?

Computational Analysis of Single Nucleotide Polymorphisms Associated with Altered Drug Responsiveness in Type 2 Diabetes

Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

Gene Therapy for Leber's Congenital Amaurosis is Safe and Effective Through 1.5 Years After Vector Administration

New somatic mutations and WNK1-B4GALNT3 gene fusion in papillary thyroid carcinoma

Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

A Homozygous Missense Mutation in the IRBP Gene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy

Molecular epidemiology of Usher syndrome in Italy

Identification and expression analysis of novel Jakmip1 transcripts

BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome

Identification and characterisation of the retinitis pigmentosa 1-like1 gene ( ): a novel candidate for retinal degenerations

Identification and characterization of C1orf36, a transcript highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa

Identification and characterisation of the retinitis pigmentosa 1-likel gene (RP1l1): a novel candidate for retinal degenerations

Imaging of adrenal tumors using FDG PET: comparison of benign and malignant lesions

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