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Comparison of simulations on the NewMexico rotor operating in pitch fault conditions

Journal of physics. Conference series, 2016-09, Vol.753 (2), p.22049

2016

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Aerodynamic drag is not the major determinant of performance during giant slalom skiing at the elite level

Scandinavian journal of medicine & science in sports, 2013-02, Vol.23 (1), p.e38-e47

2013

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P.123 - Scoliosis is an inescapable comorbidity in SMA type II. A single center experience

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S134-S134

2017

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Scoliosis is an inescapable comorbidity in SMA type II. A single center experience

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S134

2017

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Trattamento delle lesioni del rachide nel polifratturato in età pediatrica

Lo scalpello, 2014-07, Vol.28 (2), p.123-129

2014

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Il trattamento dinamico nella displasia evolutiva dell’anca

Archivio di ortopedia e reumatologia, 2012-04, Vol.123 (1), p.21-22

2012

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Nitric oxide increases the spontaneous firing rate of rat medial vestibular nucleus neurons in vitro via a cyclic GMP-mediated PKG-independent mechanism

The European journal of neuroscience, 2004-10, Vol.20 (8), p.2124-2132

2004

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δ-Thalassemia due to a Mutation in an Erythroid-Specific Binding Protein Sequence 3’ to the δ-Globin Gene

Blood, 1992-01, Vol.79 (2), p.512-516

1992

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Sardinian Gγ-HPFH: A T → C Substitution in a Conserved “Octamer” Sequence in the Gγ-Globin Promoter

Blood, 1988-03, Vol.71 (3), p.815-817

1988

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A 12-year preventive program for β-thalassemia in Northern Sardinia

Clinical genetics, 1994-09, Vol.46 (3), p.238-243

1994

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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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The Homozygous State of G to A -117Aγ Hereditary Persistence of Fetal Hemoglobin

Blood, 1989-05, Vol.73 (7), p.1999-2002

1989

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Molecular characterization of a normal Hb A2β‐thalassaemia determinant in a Sardinian family

British journal of haematology, 1987-10, Vol.67 (2), p.225-229

1987

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Retrospective clinical remarks in thalassemia intermedia

Haematologica (Roma), 1990-09, Vol.75 Suppl 5, p.9

1990

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Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy

Haematologica (Roma), 1990-09, Vol.75 Suppl 5, p.26

1990

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Iron status and anemia in thalassemic Sardinian carriers

Haematologica (Roma), 1986-01, Vol.71 (1), p.17

1986

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On the significance of hemoglobin Bart's at birth in Sicilians and Sardinians

Haematologica (Roma), 1983-07, Vol.68 (4), p.558

1983

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Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemia

American journal of hematology, 1995-08, Vol.49 (4), p.267-270

1995

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Fetal hemoglobin expression in compound heterozygotes for −117 (G→A) Aγ HPFH and β039 nonsense thalassemia

American journal of hematology, 1995-08, Vol.49 (4), p.267-270

1995

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A novel Mediterranean "delta beta-thalassemia" determinant containing the delta (+) 27 and beta (0) 39 point mutations in cis

American journal of hematology, 1994-01, Vol.45 (1), p.81-84

1994

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A novel mediterranean “δβ‐thalassemia” determinant containing the δ+27 and β°39 point mutations in cis

American journal of hematology, 1994-01, Vol.45 (1), p.81-84

1994

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Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene

Blood, 1992-01, Vol.79 (2), p.512-516

1992

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Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations

Clinical and laboratory haematology, 1992-12, Vol.14 (4), p.289-292

1992

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A frequent Aγ-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia

Human genetics, 1988-05, Vol.79 (1), p.13-17

1988

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Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations

Clinical and laboratory haematology, 1992, Vol.14 (4), p.289-292

1992

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Comparison of simulations on the NewMexico rotor operating in pitch fault conditions

Aerodynamic drag is not the major determinant of performance during giant slalom skiing at the elite level

P.123 - Scoliosis is an inescapable comorbidity in SMA type II. A single center experience

Scoliosis is an inescapable comorbidity in SMA type II. A single center experience

Trattamento delle lesioni del rachide nel polifratturato in età pediatrica

Il trattamento dinamico nella displasia evolutiva dell’anca

Nitric oxide increases the spontaneous firing rate of rat medial vestibular nucleus neurons in vitro via a cyclic GMP-mediated PKG-independent mechanism

δ-Thalassemia due to a Mutation in an Erythroid-Specific Binding Protein Sequence 3’ to the δ-Globin Gene

Sardinian Gγ-HPFH: A T → C Substitution in a Conserved “Octamer” Sequence in the Gγ-Globin Promoter

A 12-year preventive program for β-thalassemia in Northern Sardinia

Thalassemia Intermedia Resulting From a Mild β-Thalassemia Mutation

The Homozygous State of G to A -117Aγ Hereditary Persistence of Fetal Hemoglobin

Molecular characterization of a normal Hb A2β‐thalassaemia determinant in a Sardinian family

Retrospective clinical remarks in thalassemia intermedia

Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy

Iron status and anemia in thalassemic Sardinian carriers

On the significance of hemoglobin Bart's at birth in Sicilians and Sardinians

Fetal hemoglobin expression in compound heterozygotes for -117 (G-->A)A gamma HPFH and beta zero 39 nonsense thalassemia

Fetal hemoglobin expression in compound heterozygotes for −117 (G→A) Aγ HPFH and β039 nonsense thalassemia

A novel Mediterranean "delta beta-thalassemia" determinant containing the delta (+) 27 and beta (0) 39 point mutations in cis

A novel mediterranean “δβ‐thalassemia” determinant containing the δ+27 and β°39 point mutations in cis

Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene

Haematological phenotypes in a family with triplicated α-globin gene, β∘39 and δ+27 thalassaemia mutations

A frequent Aγ-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia

Haematological phenotypes in a family with triplicated alpha-globin gene, beta zero 39 and delta+27 thalassaemia mutations

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