Thalassemia traits and hemoglobinopathies in Liguria. Results of a screening

Novel path to IL-6 trans-signaling through thrombin-induced soluble IL-6 receptor release by platelets.

Journal of biological regulators and homeostatic agents·2013

Skeletal muscle cells: from local inflammatory response to active immunity.

Gene therapy·2010

Viral-load and B-lymphocyte monitoring of EBV reactivation after allogeneic hemopoietic SCT in children.

Bone marrow transplantation·2009

Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma.

British journal of cancer·2008

von Willebrand factor, von Willebrand factor-cleaving protease, and shear stress.

Cardiovascular & hematological agents in medicinal chemistry·2007

Identifying carriers of type 2N von Willebrand disease: procedures and significance.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2007

Autoimmune and inflammatory diseases associated with T-cell clonal expansion.

Haematologica·2026

Macrophage-specific LAMTOR2 deletion disrupts systemic iron homeostasis in mice.

Haematologica·2026

Dual inhibition of JAK and MEK suppresses T-cell acute lymphoblastic leukemia induced by mutant IL7R and RASGRP1 overexpression.

Haematologica·2026

Validation of the International Working Group 2023 response criteria for higher risk myelodysplastic syndromes/neoplasms using the International Consortium for Myelodysplastic Syndromes VALIDATE database and a randomized phase III trial.

Haematologica·2026

Preserving anthracycline-containing treatment in older patients with classical Hodgkin lymphoma: a role for liposomal doxorubicin. Comment on: "Age, anthracycline and mortality in 28,000 classic Hodgkin lymphoma patients: cohort study of a complete population".

Haematologica·2026

Mesenchymal stem cells in ribosomal insufficiency lead to aberrant osteoblastic differentiation and altered hematopoiesis.

Haematologica·2026

Cost-efficient long-read trio-barcoded adaptive sequencing improves rare disease diagnosis.

Nature communications·2026

High-resolution genomic architecture of a 1.71-Mb inverted SNCA triplication in a patient-derived PARK4 model.

Biochemical and biophysical research communications·2026

Mathematical Model to Assess Mutational Burden in Retinal Dystrophy Patients Negative to Mendelian Genetic Tests and Carriers of Multiple Recessive Variants.

Journal of ophthalmic & vision research·2026

A heritability-optimized method for functional prioritization of rare coding variants in complex traits.

Nature genetics·2026

WFS1 Deficiency Impairs PIAS4-Associated SUMOylation and Increases Ubiquitin-Mediated Spermatogenesis-Related Protein Degradation Leading to Testicular Male Infertility.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences-a scoping review.

Neurogenetics·2026

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Thalassemia traits and hemoglobinopathies in Liguria. Results of a screening

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Novel path to IL-6 trans-signaling through thrombin-induced soluble IL-6 receptor release by platelets.

Skeletal muscle cells: from local inflammatory response to active immunity.

Viral-load and B-lymphocyte monitoring of EBV reactivation after allogeneic hemopoietic SCT in children.

Detection of GD2-positive cells in bone marrow samples and survival of patients with localised neuroblastoma.

von Willebrand factor, von Willebrand factor-cleaving protease, and shear stress.

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Validation of the International Working Group 2023 response criteria for higher risk myelodysplastic syndromes/neoplasms using the International Consortium for Myelodysplastic Syndromes VALIDATE database and a randomized phase III trial.

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Mesenchymal stem cells in ribosomal insufficiency lead to aberrant osteoblastic differentiation and altered hematopoiesis.

Cost-efficient long-read trio-barcoded adaptive sequencing improves rare disease diagnosis.

High-resolution genomic architecture of a 1.71-Mb inverted SNCA triplication in a patient-derived PARK4 model.

Mathematical Model to Assess Mutational Burden in Retinal Dystrophy Patients Negative to Mendelian Genetic Tests and Carriers of Multiple Recessive Variants.

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