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Molecular dissection of the events leading to inactivation of the FMR1 gene

Human molecular genetics, 2005-01, Vol.14 (2), p.267-277

2005

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Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Human molecular genetics, 2012-08, Vol.21 (16), p.3647-3654

2012

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Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis

Prenatal diagnosis, 2018-12, Vol.38 (13), p.1096-1102

2018

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Meeting on data sharing for Duchenne 21–22 March 2019 Amsterdam, the Netherlands

Neuromuscular disorders : NMD, 2019-10, Vol.29 (10), p.800-810

2019

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Mutations in theCACNA1F andNYX genes in British CSNBX families

Human mutation, 2003-02, Vol.21 (2), p.169-169

2003

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Hereditary nonpolyposis colorectal cancer and related conditions

American journal of medical genetics, 2003-11, Vol.122A (4), p.325-334

2003

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Mutations in the CACNA1F and NYX genes in British CSNBX families

Human mutation, 2003-02, Vol.21 (2), p.169-169

2003

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Evidence for a New Locus for X-Linked Retinitis Pigmentosa (RP23)

Investigative ophthalmology & visual science, 2000-07, Vol.41 (8), p.2080-2086

2000

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Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

Human genetics, 1999-08, Vol.105 (1-2), p.57-62

1999

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A molecular genetic study of X-linked retinal diseases

Zito, Ilaria

2001

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Novel frameshift mutations in the RP2 gene and polymorphic variants

Human mutation, 2000-06, Vol.15 (6), p.580-580

2000

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Novel mutations of theRPGR gene in RP3 families

Human mutation, 2000-04, Vol.15 (4), p.386-386

2000

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Novel mutations of the RPGR gene in RP3 families

Human mutation, 2000-04, Vol.15 (4), p.386-386

2000

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Sequence variation within the RPGR gene: Evidence for a founder complex allele

Human mutation, 2000-09, Vol.16 (3), p.273-274

2000

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Sequence variation within theRPGR gene: Evidence for a founder complex allele

Human mutation, 2000-09, Vol.16 (3), p.273-274

2000

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Novel frameshift mutations in theRP2 gene and polymorphic variants

Human mutation, 2000-06, Vol.15 (6), p.580-580

2000

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Masitinib (AB1010), from canine tumor model to human clinical development: Where we are?

Critical reviews in oncology/hematology, 2014-07, Vol.91 (1), p.98-111

2014

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Lung inhomogeneities, inflation and [18F]2-fluoro-2-deoxy-D-glucose uptake rate in acute respiratory distress syndrome

The European respiratory journal, 2016-01, Vol.47 (1), p.233-242

2016

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Identification of a novel subpopulation of Caspase-4 positive non-small cell lung Cancer patients

Journal of experimental & clinical cancer research, 2020-11, Vol.39 (1), p.1-17, Article 242

2020

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Infiltrating mast cells correlate with angiogenesis in bone metastases from gastric cancer patients

International journal of molecular sciences, 2015-02, Vol.16 (2), p.3237-3250

2015

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SERS Quantification of Galunisertib Delivery in Colorectal Cancer Cells by Plasmonic‐Assisted Diatomite Nanoparticles

Small (Weinheim an der Bergstrasse, Germany), 2021-08, Vol.17 (34), p.e2101711-n/a

2021

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Epidemiology of ventilator-associated pneumonia in ICU COVID-19 patients: an alarming high rate of multidrug-resistant bacteria

Journal of Anesthesia, Analgesia and Critical Care (Online), 2022-08, Vol.2 (1), p.36-36, Article 36

2022

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2936: SABR for ES-NSCLC in very elderly (≥80 years old) patients: results on 18 years of experience

Radiotherapy and oncology, 2024-05, Vol.194, p.S1792-S1795

2024

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Beta-blockers are associated with better long-term survival in patients with Takotsubo syndrome

Heart (British Cardiac Society), 2022-09, Vol.108 (17), p.1369-1376

2022

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Relative lymphocyte count as an indicator of 3-year mortality in elderly people with severe COPD

BMC pulmonary medicine, 2018-07, Vol.18 (1), p.116-116, Article 116

2018

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Molecular dissection of the events leading to inactivation of the FMR1 gene

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis

Meeting on data sharing for Duchenne 21–22 March 2019 Amsterdam, the Netherlands

Mutations in theCACNA1F andNYX genes in British CSNBX families

Hereditary nonpolyposis colorectal cancer and related conditions

Mutations in the CACNA1F and NYX genes in British CSNBX families

Evidence for a New Locus for X-Linked Retinitis Pigmentosa (RP23)

Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

A molecular genetic study of X-linked retinal diseases

Novel frameshift mutations in the RP2 gene and polymorphic variants

Novel mutations of theRPGR gene in RP3 families

Novel mutations of the RPGR gene in RP3 families

Sequence variation within the RPGR gene: Evidence for a founder complex allele

Sequence variation within theRPGR gene: Evidence for a founder complex allele

Novel frameshift mutations in theRP2 gene and polymorphic variants

Masitinib (AB1010), from canine tumor model to human clinical development: Where we are?

Lung inhomogeneities, inflation and [18F]2-fluoro-2-deoxy-D-glucose uptake rate in acute respiratory distress syndrome

Identification of a novel subpopulation of Caspase-4 positive non-small cell lung Cancer patients

Infiltrating mast cells correlate with angiogenesis in bone metastases from gastric cancer patients

SERS Quantification of Galunisertib Delivery in Colorectal Cancer Cells by Plasmonic‐Assisted Diatomite Nanoparticles

Epidemiology of ventilator-associated pneumonia in ICU COVID-19 patients: an alarming high rate of multidrug-resistant bacteria

2936: SABR for ES-NSCLC in very elderly (≥80 years old) patients: results on 18 years of experience

Beta-blockers are associated with better long-term survival in patients with Takotsubo syndrome

Relative lymphocyte count as an indicator of 3-year mortality in elderly people with severe COPD

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