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Inherited thrombocytopenias frequently diagnosed in adults

Journal of thrombosis and haemostasis, 2013-06, Vol.11 (6), p.1006-1019

2013

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Design of an Industrially Feasible Twisted-Stack HTS Cable-in-Conduit Conductor for Fusion Application

IEEE transactions on applied superconductivity, 2014-06, Vol.24 (3), p.1-5

2014

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IEEE_Xplore

Synthesis and anticancer activity of some 8-substituted-7-methoxy-2H-chromen-2-one derivatives toward hepatocellular carcinoma HepG2 cells

European journal of medicinal chemistry, 2015-01, Vol.90, p.221-231

2015

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Synthesis, in vitro anticancer activity and in silico studies of certain isoxazole-based carboxamides, ureates, and hydrazones as potential inhibitors of VEGFR2

Bioorganic chemistry, 2021-11, Vol.116, p.105334-105334, Article 105334

2021

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Design, synthesis and vasorelaxant evaluation of novel coumarin–pyrimidine hybrids

Bioorganic & medicinal chemistry, 2011-10, Vol.19 (20), p.6087-6097

2011

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Electrical Characterization of ENEA High Temperature Superconducting Cable

IEEE transactions on applied superconductivity, 2015-06, Vol.25 (3), p.1-4

2015

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IEEE_Xplore

Synthesis of novel thiadiazole derivatives as selective COX-2 inhibitors

MedChemComm, 2016-01, Vol.7 (12), p.2309-2327

2016

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Weekly combination of non-pegylated liposomal doxorubicin and taxane in first-line breast cancer: wALT trial (phase I–II)

Annals of oncology, 2011-02, Vol.22 (2), p.315-320

2011

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Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

Haematologica (Roma), 2007-09, Vol.92 (9), p.1186-1193

2007

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GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

Clinical genetics, 2007-11, Vol.72 (5), p.427-433

2007

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RETRACTED: Identification of novel aminothiazole and aminothiadiazole conjugated cyanopyridines as selective CHK1 inhibitors

European journal of medicinal chemistry, , Vol.92, p.459-470

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Phase III Randomized Trial of FOLFIRI Versus FOLFOX4 in the Treatment of Advanced Colorectal Cancer: A Multicenter Study of the Gruppo Oncologico Dell’Italia Meridionale

Journal of clinical oncology, 2005-08, Vol.23 (22), p.4866-4875

2005

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Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes

European journal of neurology, 2008-05, Vol.15 (5), p.520-524

2008

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Synthesis and biological evaluation of imidazolylmethylacridones as cytochrome P-450 enzymes inhibitors

MedChemComm, 2012-06, Vol.3 (6), p.663

2012

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Characterization of a murine gene homologous to the bovine CaCC chloride channel

Gene, 1999-03, Vol.228 (1), p.181-188

1999

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Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

Thrombosis and haemostasis, 2010-04, Vol.103 (4), p.826

2010

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Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

Journal of medical genetics, 2000-07, Vol.37 (7), p.e9-9

2000

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SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2

Brain (London, England : 1878), 2006-01, Vol.129 (1), p.235-242

2006

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Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

Nature genetics, 2000-09, Vol.26 (1), p.103-105

Syndrome Consortium, The May-Hegglin/Fechtner

2000

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Clinical and genetic characterization of Chanarin–Dorfman syndrome

Biochemical and biophysical research communications, 2008-05, Vol.369 (4), p.1125-1128

2008

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Changes in Cardiac Function and Cerebral Blood Flow in Relation to Peri/Intraventricular Hemorrhage in Extremely Preterm Infants

The Journal of pediatrics, 2014-02, Vol.164 (2), p.264-270.e3

2014

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Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene

Kidney international, 2004-05, Vol.65 (5), p.1598-1603

2004

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Communicating cancer diagnosis and prognosis: When the target is the elderly patient-a GIOGer study

European journal of cancer (1990), 2009-02, Vol.45 (3), p.374-383

2009

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Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

Nature (London), 1994-01, Vol.367 (6461), p.377-378

1994

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Neonatal Blood Pressure Support: The Use of Inotropes, Lusitropes, and Other Vasopressor Agents

Clinics in perinatology, 2012-03, Vol.39 (1), p.221-238

2012

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Inherited thrombocytopenias frequently diagnosed in adults

Design of an Industrially Feasible Twisted-Stack HTS Cable-in-Conduit Conductor for Fusion Application

Synthesis and anticancer activity of some 8-substituted-7-methoxy-2H-chromen-2-one derivatives toward hepatocellular carcinoma HepG2 cells

Synthesis, in vitro anticancer activity and in silico studies of certain isoxazole-based carboxamides, ureates, and hydrazones as potential inhibitors of VEGFR2

Design, synthesis and vasorelaxant evaluation of novel coumarin–pyrimidine hybrids

Electrical Characterization of ENEA High Temperature Superconducting Cable

Synthesis of novel thiadiazole derivatives as selective COX-2 inhibitors

Weekly combination of non-pegylated liposomal doxorubicin and taxane in first-line breast cancer: wALT trial (phase I–II)

Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease

RETRACTED: Identification of novel aminothiazole and aminothiadiazole conjugated cyanopyridines as selective CHK1 inhibitors

Phase III Randomized Trial of FOLFIRI Versus FOLFOX4 in the Treatment of Advanced Colorectal Cancer: A Multicenter Study of the Gruppo Oncologico Dell’Italia Meridionale

Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genes

Synthesis and biological evaluation of imidazolylmethylacridones as cytochrome P-450 enzymes inhibitors

Characterization of a murine gene homologous to the bovine CaCC chloride channel

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22–q11.2

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

Clinical and genetic characterization of Chanarin–Dorfman syndrome

Changes in Cardiac Function and Cerebral Blood Flow in Relation to Peri/Intraventricular Hemorrhage in Extremely Preterm Infants

Autosomal-dominant Alport syndrome: Natural history of a disease due to COL4A3 or COL4A4 gene

Communicating cancer diagnosis and prognosis: When the target is the elderly patient-a GIOGer study

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

Neonatal Blood Pressure Support: The Use of Inotropes, Lusitropes, and Other Vasopressor Agents

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