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Ex vivo evaluation of four final irrigation protocols on the removal of hard‐tissue debris from the mesial root canal system of mandibular first molars

International endodontic journal, 2017-04, Vol.50 (4), p.398-406

2017

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Root canal morphology of primary molars: a micro-computed tomography study

European archives of paediatric dentistry, 2014-10, Vol.15 (5), p.317-326

2014

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Transitory Activation of the Central and Ovarian Norepinephrine Systems During Cold Stress-Induced Polycystic Ovary in Rats

Journal of neuroendocrinology, 2013-01, Vol.25 (1), p.23-33

2013

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Cholelithiasis and Gilbert's syndrome in homozygous β‐thalassaemia

British journal of haematology, 2001-12, Vol.115 (4), p.926-928

2001

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Evaluation of bond strength in single‐cone fillings of canals with different cross‐sections

International endodontic journal, 2017-02, Vol.50 (2), p.177-183

2017

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Influence of therapeutic cancer radiation on the bond strength of an epoxy- or an MTA-based sealer to root dentine

International endodontic journal, 2016-11, Vol.49 (11), p.1065-1072

2016

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Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution

Annals of human genetics, 1997-09, Vol.61 (5), p.411-424, Article S0003480097006477

1997

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Identification of a Novel Mutation (S13F) in the CFTR Gene in a CF Patient of Sardinian Origin

Human mutation, 1998, Vol.11 (4), p.337-337

1998

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Molecular screening and fetal diagnosis of β-thalassemia in the Italian population

Human genetics, 1992-08, Vol.89 (6), p.585-589

1992

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Two novel mutations in the transmembrane domains of the CFTR gene in subjects of Sardinian descent

Human molecular genetics, 1993-10, Vol.2 (10), p.1739-1740

1993

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Ovariectomy Exacerbates Apical Periodontitis in Rats with an Increase in Expression of Proinflammatory Cytokines and Matrix Metalloproteinases

Journal of endodontics, 2018-05, Vol.44 (5), p.780-785

2018

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Quantitative Assessment of 2-dimensional Parameters in Tomographic Images by Using Different Segmentation Methods

Journal of endodontics, 2020-05, Vol.46 (5), p.694-699

2020

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A decisional algorithm to start iron chelation in patients with beta thalassemia

Haematologica (Roma), 2014-03, Vol.99 (3), p.e38-e40

2014

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Heterozygous β‐thalassemia: Relationship between the hematological phenotype and the type of β‐thalassemia mutation

American journal of hematology, 1992-01, Vol.39 (1), p.1-4

1992

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A novel cystic fibrosis mutation: deletion of seventeen nucleotides at the exon 10-intron 10 boundary of the CFTR gene, in a Sardinian patient

Human molecular genetics, 1993-01, Vol.2 (1), p.83-84

1993

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Beta thalassaemia mutations in Sardinians: implications for prenatal diagnosis

Journal of medical genetics, 1987-02, Vol.24 (2), p.97-100

1987

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Thalassemia Intermedia Resulting From a Mild β-Thalassemia Mutation

Blood, 1989-02, Vol.73 (2), p.601-605

1989

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CBCT-based assessment of root canal treatment using micro-CT reference images

Imaging science in dentistry, 2022-09, Vol.52 (3), p.245-258

2022

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A specific cystic fibrosis mutation (T338I) associated with the phenotype of isolated hypotonic dehydration

The Journal of pediatrics, 1995-08, Vol.127 (2), p.281-283

1995

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Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populations

Journal of medical genetics, 1988-11, Vol.25 (11), p.762-765

1988

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Molecular bases for cystic fibrosis in the Sardinian population

Human genetics, 1990-09, Vol.85 (4), p.415-415

1990

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Molecular basis of beta-thalassemia intermedia in a southern Italian region (Puglia)

Acta haematologica, 1991-01, Vol.86 (4), p.174-178

1991

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Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations

Human mutation, 1997, Vol.10 (2), p.135-154

1997

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Problems in prenatal diagnosis of β-thalassaemia by fetal blood analysis: β-chain variant comigrating with gamma chains

Prenatal diagnosis, 1988-06, Vol.8 (5), p.393-397

1988

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Prenatal diagnosis of beta-thalassemia in Italian population

Haematologica (Roma), 1988-09, Vol.73 (5), p.331

1988

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Ex vivo evaluation of four final irrigation protocols on the removal of hard‐tissue debris from the mesial root canal system of mandibular first molars

Root canal morphology of primary molars: a micro-computed tomography study

Transitory Activation of the Central and Ovarian Norepinephrine Systems During Cold Stress-Induced Polycystic Ovary in Rats

Cholelithiasis and Gilbert's syndrome in homozygous β‐thalassaemia

Evaluation of bond strength in single‐cone fillings of canals with different cross‐sections

Influence of therapeutic cancer radiation on the bond strength of an epoxy- or an MTA-based sealer to root dentine

Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution

Identification of a Novel Mutation (S13F) in the CFTR Gene in a CF Patient of Sardinian Origin

Molecular screening and fetal diagnosis of β-thalassemia in the Italian population

Two novel mutations in the transmembrane domains of the CFTR gene in subjects of Sardinian descent

Ovariectomy Exacerbates Apical Periodontitis in Rats with an Increase in Expression of Proinflammatory Cytokines and Matrix Metalloproteinases

Quantitative Assessment of 2-dimensional Parameters in Tomographic Images by Using Different Segmentation Methods

A decisional algorithm to start iron chelation in patients with beta thalassemia

Heterozygous β‐thalassemia: Relationship between the hematological phenotype and the type of β‐thalassemia mutation

A novel cystic fibrosis mutation: deletion of seventeen nucleotides at the exon 10-intron 10 boundary of the CFTR gene, in a Sardinian patient

Beta thalassaemia mutations in Sardinians: implications for prenatal diagnosis

Thalassemia Intermedia Resulting From a Mild β-Thalassemia Mutation

CBCT-based assessment of root canal treatment using micro-CT reference images

A specific cystic fibrosis mutation (T338I) associated with the phenotype of isolated hypotonic dehydration

Prenatal diagnosis of beta thalassaemia by oligonucleotide analysis in Mediterranean populations

Molecular bases for cystic fibrosis in the Sardinian population

Molecular basis of beta-thalassemia intermedia in a southern Italian region (Puglia)

Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations

Problems in prenatal diagnosis of β-thalassaemia by fetal blood analysis: β-chain variant comigrating with gamma chains

Prenatal diagnosis of beta-thalassemia in Italian population

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