Prevention of thalassaemia major in Latium (Italy)

Survey on the usage of therapeutic erythrocytapheresis in transfusion services in Italy for the treatment of polycythemia vera, secondary erythrocytosis and hemochromatosis.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis·2023

Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption.

Bone·2021

In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS).

Neurogenetics·2018

C-reactive protein: a marker of neonatal stress?

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians·2013

Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.

International journal of laboratory hematology·2013

Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium example.

Prenatal diagnosis·2009

Switch to injectable cabotegravir-rilpivirine given every 8 weeks in adolescents living with HIV with virological suppression in sub-Saharan Africa (LATA): a randomised, open-label, multicentre, 96-week non-inferiority trial.

Lancet (London, England)·2026

Most-favoured-nation pricing for prescription drugs in US Medicare: a cohort study.

Lancet (London, England)·2026

Complete chloroplast genome sequence and phylogenetic analysis of Chrysosplenium insularis J. E. Jang, K. H. Lee & H. Y. Gil (Saxifragaceae), an endemic Korean species.

Mitochondrial DNA. Part B, Resources·2026

Proteogenomic Profiling of Idiopathic Pulmonary Arterial Hypertension Identifies Sex-Differential Proteins and Candidate Therapeutic Targets.

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

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

Psychiatric genetics·2026

Leucine-rich glioma inactivated 1 (LGI1) is a ganglioside-binding protein.

FEBS letters·2026

Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort.

International journal of molecular sciences·2026

The genome sequence of the Tufted Button, Acleris cristana (Denis & Schiffermüller, 1775).

Wellcome open research·2026

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Prevention of thalassaemia major in Latium (Italy)

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Survey on the usage of therapeutic erythrocytapheresis in transfusion services in Italy for the treatment of polycythemia vera, secondary erythrocytosis and hemochromatosis.

Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption.

In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS).

C-reactive protein: a marker of neonatal stress?

Interpreting elevated fetal hemoglobin in pathology and health at the basic laboratory level: new and known γ- gene mutations associated with hereditary persistence of fetal hemoglobin.

Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium example.

Switch to injectable cabotegravir-rilpivirine given every 8 weeks in adolescents living with HIV with virological suppression in sub-Saharan Africa (LATA): a randomised, open-label, multicentre, 96-week non-inferiority trial.

Most-favoured-nation pricing for prescription drugs in US Medicare: a cohort study.

Complete chloroplast genome sequence and phylogenetic analysis of Chrysosplenium insularis J. E. Jang, K. H. Lee & H. Y. Gil (Saxifragaceae), an endemic Korean species.

Proteogenomic Profiling of Idiopathic Pulmonary Arterial Hypertension Identifies Sex-Differential Proteins and Candidate Therapeutic Targets.

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

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Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort.

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Prevention of thalassaemia major in Latium (Italy)

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