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Deep sequencing reveals double mutations in cis of MPL exon 10 in myeloproliferative neoplasms

Haematologica (Roma), 2011-04, Vol.96 (4), p.607-611

2011

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Foucault, the Iranian Uprising and the Constitution of a Collective Subjectivity

Foucault studies, 2018-10 (25), p.299-311

2018

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A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer

PloS one, 2013-03, Vol.8 (3), p.e59939-e59939

2013

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Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulation

Haematologica (Roma), 2011-10, Vol.96 (10), p.1424-1432

2011

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Transfiguration et critique : Foucault, Baudelaire et l’ontologie du présent

Theory Now (Online), 2020-01, Vol.3 (1), p.161-173

Cremonesi, Laura

2020

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Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis

Haematologica (Roma), 2007-08, Vol.92 (8), p.1037-1042

2007

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Advancing the education in molecular diagnostics: The IFCC-Initiative “Clinical Molecular Biology Curriculum” (C-CMBC); A ten-year experience

Clinica chimica acta, 2014-09, Vol.436, p.5-8

2014

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Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations

Clinical chemistry and laboratory medicine, 2012-06, Vol.50 (6), p.1021-1029

2012

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The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects

Haematologica (Roma), 2010-05, Vol.95 (5), p.849-850

2010

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Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of β-thalassemia

Haematologica (Roma), 2008-04, Vol.93 (4), p.610-614

2008

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Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia

Blood, 2014-08, Vol.124 (9), p.1513-1521

2014

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Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer

BMC genomics, 2008-10, Vol.9 (1), p.464-464, Article 464

2008

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Prospective evaluation of RASSF1A cell-free DNA as a biomarker of pre-eclampsia

Placenta (Eastbourne), 2015-09, Vol.36 (9), p.996-1001

2015

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Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders

Blood, 2008-02, Vol.111 (3), p.1686-1689

2008

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Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology

Clinical chemistry (Baltimore, Md.), 2002-12, Vol.48 (12), p.2124-2130

2002

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COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma

Journal of medical genetics, 2016-07, Vol.53 (7), p.481-487

2016

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Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson’s Disease and Other Movement Disorders

Parkinson's disease, 2011-01, Vol.2011 (2011), p.786-791

2011

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Communicating Down syndrome risk according to maternal age: "1-in-X" effect on perceived risk

Prenatal diagnosis, 2015-08, Vol.35 (8), p.777-782

2015

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Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseases

Clinical chemistry (Baltimore, Md.), 2011-01, Vol.57 (1), p.136-138

2011

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Foucault, the Iranian Uprising and the Constitution of a Collective Subjectivity

Foucault studies, 2018-10 (25), p.299

2018

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Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis

Blood, 2009-10, Vol.114 (17), p.3538-3545

2009

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Evaluation of different approaches for fetal DNA analysis from maternal plasma and nucleated blood cells

Clinical chemistry (Baltimore, Md.), 1999-09, Vol.45 (9), p.1570-1572

1999

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HIF1A and MIF as potential predictive mRNA biomarkers of pre-eclampsia: a longitudinal prospective study in high risk population

Clinical chemistry and laboratory medicine, 2015-08, Vol.53 (9), p.1339

2015

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Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case report

Clinical chemistry and laboratory medicine, 2014-04, Vol.52 (4), p.505

2014

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Regression of symptoms after selective iron chelation therapy in a case of neurodegeneration with brain iron accumulation

Movement disorders, 2008-04, Vol.23 (6), p.904-907

2008

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Deep sequencing reveals double mutations in cis of MPL exon 10 in myeloproliferative neoplasms

Foucault, the Iranian Uprising and the Constitution of a Collective Subjectivity

A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer

Over-expression of mitochondrial ferritin affects the JAK2/STAT5 pathway in K562 cells and causes mitochondrial iron accumulation

Transfiguration et critique : Foucault, Baudelaire et l’ontologie du présent

Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis

Advancing the education in molecular diagnostics: The IFCC-Initiative “Clinical Molecular Biology Curriculum” (C-CMBC); A ten-year experience

Study of FTMT and ABCA4 genes in a patient affected by age-related macular degeneration: identification and analysis of new mutations

The -582A>G variant of the HAMP promoter is not associated with high serum ferritin levels in normal subjects

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of β-thalassemia

Driver somatic mutations identify distinct disease entities within myeloid neoplasms with myelodysplasia

Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer

Prospective evaluation of RASSF1A cell-free DNA as a biomarker of pre-eclampsia

Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders

Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology

COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma

Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson’s Disease and Other Movement Disorders

Communicating Down syndrome risk according to maternal age: "1-in-X" effect on perceived risk

Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseases

Foucault, the Iranian Uprising and the Constitution of a Collective Subjectivity

Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis

Evaluation of different approaches for fetal DNA analysis from maternal plasma and nucleated blood cells

HIF1A and MIF as potential predictive mRNA biomarkers of pre-eclampsia: a longitudinal prospective study in high risk population

Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case report

Regression of symptoms after selective iron chelation therapy in a case of neurodegeneration with brain iron accumulation

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