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1 Contributo su Rivista 7529
- 1.1 Articolo in rivista 6680
- 1.2 Recensione in rivista 532
- 1.3 Scheda bibliografica 0
- 1.4 Nota a sentenza 6
- 1.5 Abstract in rivista 310
- 1.6 Traduzione in rivista 1

2 Contributo in Volume 281

3 Libro 135
- 3.1 Monografia o trattato scientifico 127
- 3.2 Concordanza 0
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- 3.4 Bibliografia 0
- 3.5 Edizione critica 1
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- 3.7 Commento scientifico 0
- 3.8 Traduzione di libro 7

4 Contributo in Atti di Convegno (Proceeding) 651
- 4.1 Contributo in Atti di convegno 186
- 4.2 Abstract in Atti di convegno 385
- 4.3 Poster 80

5 Altro 13
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6 Brevetti 21
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7 Curatele 16
- 7.1 Curatela 16

Prodotti recenti

Assessing gut barrier integrity and reproductive performance following pre-mating oral administration of solid-lipid-nanoparticles designed for drug delivery

Solid lipid nanoparticles (SLNs) have gained interest as drug delivery carriers due to their efficient cellular internalization and increased therapeutic effect of the loaded drug, with minimal side effects. Although recently several studies have shown the possibility to administer SLNs during pregnancy to vehicle mRNA to the placenta, data about the effect of premating exposure to SLNs on pregnancy outcome are scant. Considering that assumption of drug-delivering nanocarriers in reproductive...

Unexpected macrophage activation syndrome in a healthy young woman: a case report

Macrophage activation syndrome (MAS) is a life-threatening condition and a medical emergency with a high-risk of mortality. It belongs to a group of diseases known as "hemophagocytic lymphohistiocytosis", characterized by a cytokine storm, with secretion of tumor necrosis factor, interleukins and interferon-gamma, and an inappropriate activation of macrophages and T-lymphocytes. Some inflammatory and systemic autoimmune diseases, such as systemic juvenile idiopathic arthritis, Still's disease...

Microcephalic osteodysplastic primordial dwarfism typeIIand pachygyria: Morphometric analysis in a 2-year-old girl

Microcephalic osteodysplastic primordial dwarfism (MOPD) type II is a rare disorder characterized by skeletal dysplasia, severe proportionate short stature, insulin resistance and cerebrovascular abnormalities including cerebral aneurysms and moyamoya disease. MOPD type II is caused by mutations in the pericentrin (PCNT) gene, which encodes a protein involved in centrosomes function. We report a 2 year old girl affected by MOPD type II caused by two compound heterozygous loss-of-function vari...

The splice c.1815G > A variant in KIAA0586 results in a phenotype bridging short-rib-polydactyly and oral-facial-digital syndrome A case report and literature review

Introduction: KIAA0586 variants have been associated to short-rib thoracic dysplasia, an autosomal recessive skeletal ciliopathy characterized by a narrow thorax, short limbs, and radiological skeletal abnormalities. Patient concerns: Patients 1 and 2 were two Roma Gypsy siblings presenting thoracic dysplasia and a combination of oral cavity anomalies. Diagnosis: A custom NGS gene panel, including genes associated to skeletal ciliopathies, identified the homozygous KIAA0586 splicing variant c...

GRADE guidelines: 21 part 2. Test accuracy: inconsistency, imprecision, publication bias, and other domains for rating the certainty of evidence and presenting it in evidence profiles and summary of findings tables

Objectives: This article provides updated GRADE guidance about how authors of systematic reviews and health technology assessments and guideline developers can rate the certainty of evidence (also known as quality of the evidence or confidence in the estimates) of a body of evidence addressing test accuracy (TA) on the domains imprecision, inconsistency, publication bias, and other domains. It also provides guidance for how to present synthesized information in evidence profiles and summary o...

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