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A performance-based framework for adaptive seismic aftershock risk assessment

Earthquake engineering & structural dynamics, 2014-11, Vol.43 (14), p.2179-2197

2014

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Activated Platelet‐Derived and Leukocyte‐Derived Circulating Microparticles and the Risk of Thrombosis in Heparin‐Induced Thrombocytopenia: A Role for PF4‐Bearing Microparticles?

Cytometry. Part B, Clinical cytometry, 2018-03, Vol.94 (2), p.334-341

2018

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New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia

British journal of haematology, 2019-03, Vol.184 (5), p.855-858

2019

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Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA‐DRB111 and DQB103 antigens

British journal of haematology, 2018-10, Vol.183 (2), p.317-319

2018

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Thrombopoietin receptor agonists as second-line therapy in splenectomy-eligible persistent immune thrombocytopenia: a case series

Blood coagulation & fibrinolysis, 2019-09, Vol.30 (6), p.295-299

2019

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Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations

British journal of haematology, 2019-08, Vol.186 (4), p.e100-e103

2019

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Occurrence of thrombosis in congenital thrombocytopenic disorders: a critical annotation of the literature

Blood coagulation & fibrinolysis, 2013-01, Vol.24 (1), p.18-22

2013

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A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15

Blood coagulation & fibrinolysis, 2014-03, Vol.25 (2), p.191-195

2014

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Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1alpha )PDH gene expression in rat

American journal of physiology: endocrinology and metabolism, 1999-05, Vol.276 (5), p.E922-E929

1999

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Presence of anti-ADAMTS13 antibodies in obesity

European journal of clinical investigation, 2012-11, Vol.42 (11), p.1197-1204

2012

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New heterozygous variant in GP 1 BB gene is responsible for an inherited form of macrothrombocytopenia

British journal of haematology, 2019-03, Vol.184 (5), p.855-858

2019

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Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA ‐ DRB 111 and DQB 103 antigens

British journal of haematology, 2018-10, Vol.183 (2), p.317-319

2018

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THE BOLOMETER AND THE SPECTRO-BOLOMETER AS STEPS TOWARDS THE BLACK-BODY SPECTRUM

Nuncius, 2003, Vol.18 (2), p.825-840

LOMBARDI, ANNA M.

2003

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Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)

Cardiovascular & hematological disorders drug targets, 2017-08, Vol.17 (2)

2017

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Different velocities in wave trains: early definitions and interpretations

Journal of optics. B, Quantum and semiclassical optics, 2002-08, Vol.4 (4), p.S473-S476, Article 342

Lombardi, Anna M

2002

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THE BOLOMETER AND THE SPECTRO-BOLOMETER AS STEPS TOWARDS THE BLACK-BODY SPECTRUM

Nuncius, 2003-01, Vol.18 (2), p.825-840

LOMBARDI, ANNA M.

2003

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Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1α)PDH gene expression in rat

American journal of physiology: endocrinology and metabolism, 1999-05, Vol.39 (5), p.E922-E929

1999

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Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1α)PDH gene expression in rat

American journal of physiology: endocrinology and metabolism, 1999-05, Vol.276 (5), p.E922

1999

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Anomalies and transient variations of b-value in Italy during the major earthquake sequences: what truth is there to this?

Geophysical journal international, 2023-11, Vol.232 (3), p.1545-1555

Lombardi, A M

2023

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Procedural Outcomes of Revascularization of Chronic Total Occlusion of Native Coronary Arteries (from a Multicenter United States Registry)

The American journal of cardiology, 2013-08, Vol.112 (4), p.488-492

2013

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Gain-of-function Naᵥ1.8 mutations in painful neuropathy

Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (47), p.19444-19449

2012

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“The final countdown”: Is intraoperative, intermittent neuromonitoring really useful in preventing permanent nerve palsy? Evidence from a meta-analysis

Surgery, 2016-12, Vol.160 (6), p.1693-1706

2016

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Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

Lancet neurology, 2020-02, Vol.19 (2), p.145-156

2020

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CAR T-cell-mediated delivery of bispecific innate immune cell engagers for neuroblastoma

Nature communications, 2024-08, Vol.15 (1), p.7141-19

2024

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A performance-based framework for adaptive seismic aftershock risk assessment

Activated Platelet‐Derived and Leukocyte‐Derived Circulating Microparticles and the Risk of Thrombosis in Heparin‐Induced Thrombocytopenia: A Role for PF4‐Bearing Microparticles?

New heterozygous variant in GP1BB gene is responsible for an inherited form of macrothrombocytopenia

Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA‐DRB111 and DQB103 antigens

Thrombopoietin receptor agonists as second-line therapy in splenectomy-eligible persistent immune thrombocytopenia: a case series

Genetic analysis of erythrocytosis reveals possible causative and modifier gene mutations

Occurrence of thrombosis in congenital thrombocytopenic disorders: a critical annotation of the literature

A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15

Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1alpha )PDH gene expression in rat

Presence of anti-ADAMTS13 antibodies in obesity

New heterozygous variant in GP 1 BB gene is responsible for an inherited form of macrothrombocytopenia

Familial acquired thrombotic thrombocytopenic purpura: immunogenetic link with HLA ‐ DRB 111 and DQB 103 antigens

THE BOLOMETER AND THE SPECTRO-BOLOMETER AS STEPS TOWARDS THE BLACK-BODY SPECTRUM

Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T)

Different velocities in wave trains: early definitions and interpretations

THE BOLOMETER AND THE SPECTRO-BOLOMETER AS STEPS TOWARDS THE BLACK-BODY SPECTRUM

Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1α)PDH gene expression in rat

Hyperlactatemia reduces muscle glucose uptake and GLUT-4 mRNA while increasing (E1α)PDH gene expression in rat

Anomalies and transient variations of b-value in Italy during the major earthquake sequences: what truth is there to this?

Procedural Outcomes of Revascularization of Chronic Total Occlusion of Native Coronary Arteries (from a Multicenter United States Registry)

Gain-of-function Naᵥ1.8 mutations in painful neuropathy

“The final countdown”: Is intraoperative, intermittent neuromonitoring really useful in preventing permanent nerve palsy? Evidence from a meta-analysis

Application of the “Hybrid Approach” to Chronic Total Occlusions in Patients With Previous Coronary Artery Bypass Graft Surgery (from a Contemporary Multicenter US Registry)

Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

CAR T-cell-mediated delivery of bispecific innate immune cell engagers for neuroblastoma

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