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sFlt-1/PlGF ratio use does not reduce hospitalisation duration in suspected preeclampsia: the PRECOG study, a multicentre randomised trial.

Scientific reports·2025

Novel genetic mutation associated with hyperphosphatemic familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome treated with denosumab: a case report.

Reumatismo·2024

Clinical-Hematological Changes and Predictors of Severity in Acute Food Protein-Induced Enterocolitis Syndrome Reactions at Oral Food Challenge: A Multicenter Observational Study.

The journal of allergy and clinical immunology. In practice·2024

Rhinitis associated with asthma is distinct from rhinitis alone: The ARIA-MeDALL hypothesis.

Allergy·2023

Antenatal screening of small for gestational age: Impact on obstetrical management and neonatal outcomes in case of trial of labor after 37 weeks.

Journal of gynecology obstetrics and human reproduction·2021

Intervertebral disc and endplate cells response to IL-1β inflammatory cell priming and identification of molecular targets of tissue degeneration.

European cells & materials·2020

Developmental and behavioral profile in a domestic adoptees sample: a new challenge for the pediatrician.

Minerva pediatrica·2020

A new approach to the diagnosis of short stature.

Minerva pediatrica·2020

Kounis Syndrome: a pediatric perspective.

Minerva pediatrica·2020

Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

Minerva pediatrica·2020

Tall stature in children and adolescents.

Minerva pediatrica·2020

Precocious puberty.

Minerva pediatrica·2020

Selective Limbic and Striatal Atrophy Corresponds to Regional Gene Expression in Leucine-Rich Glioma-Inactivated-1 Immunoglobulin G Autoimmune Encephalitis.

Annals of neurology·2026

Draft genome sequence of the moderately halophilic bacterium Vreelandella alkaliphila strain WG10-512 isolated from a Himalayan salt mine in India.

Microbiology resource announcements·2026

Genetic variation in IL-6 rs1800796 and its association with non-Hodgkin lymphoma susceptibility in the Egyptian population.

Journal of biosciences·2026

Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

Japanese journal of ophthalmology·2026

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

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sFlt-1/PlGF ratio use does not reduce hospitalisation duration in suspected preeclampsia: the PRECOG study, a multicentre randomised trial.

Novel genetic mutation associated with hyperphosphatemic familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome treated with denosumab: a case report.

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Human inborn errors of immunity caused by defects of receptor and proteins of cellular membrane.

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Precocious puberty.

Selective Limbic and Striatal Atrophy Corresponds to Regional Gene Expression in Leucine-Rich Glioma-Inactivated-1 Immunoglobulin G Autoimmune Encephalitis.

Draft genome sequence of the moderately halophilic bacterium Vreelandella alkaliphila strain WG10-512 isolated from a Himalayan salt mine in India.

Genetic variation in IL-6 rs1800796 and its association with non-Hodgkin lymphoma susceptibility in the Egyptian population.

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