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Mario Giordano

Biographic Data

ID7622302
NAMEMario Giordano
GIVEN NAMESMario
FAMILY NAMEGiordano
SIGNATUREGIORDANO M
AFFILIATIONSOspedale Pediatrico Giovanni XXIII
ORCID0000-0003-4224-636X
VERIFIEDYes
TOTAL WORKS5
TOTAL CITATIONS0
WORKS AS AUTHOR5
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Animal-Assisted Psychoeducational Intervention in Paediatric Oncohaematology

    Open Access•Chiara Battaglini, Valentina Isaja et al.•ARTICLE•Children•2026

    Background : Hospitalisation for paediatric oncohaematological diseases entails significant physical and psychological stress, often compromising children's emotional regulation and daily functioning. In this context, complementary interventions can provide additional support to the clinical work conducted with children and adolescents undergoing treatment, fostering emotional awareness and well-being. This study evaluates the feasibility and per…

  • Anomalous Coronary Artery Origin from Pulmonary Artery and Coronary Fistulas

    Open Access•Mario Giordano, Martina Evangelista et al.•ARTICLE•Children•2026

    Anomalous coronary artery origin from pulmonary artery and coronary-pulmonary fistulas are the major causes of ischemic cardiopathy in children. Both anomalies are characterized by a connection between a higher and a lower pressure chamber causing coronary steal. However, several mechanisms and associated lesions may be responsible of the different presentations of the "coronary steal phenomenon". The aim of this review is to highlight the differ…

  • Unusual Onset of Hereditary Hemorrhagic Telangiectasia Due to Somatic Mutational Mosaicism

    Open Access•Virginia Mirra, Margherita Rosa et al.•ARTICLE•Children•2025

    Hereditary Hemorrhagic Telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a disorder of angiogenesis characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations. This rare autosomal dominant disorder is caused by pathogenic variants in the ENG and ACVRL1 genes, and only 1-3% of case variants occur in SMAD4 . HHT clinical manifestations include telangiectasias, epistaxis, and arteriovenous malformations …

  • Incidence and Prevalence of Multisystem Inflammatory Syndrome in Children (MIS-C) in Southern Italy

    Open Access•Francesco La Torre, Maria Pia Elicio et al.•ARTICLE•Children•2023

    Multisystem inflammatory syndrome in children (MIS-C) is a pediatric hyperinflammatory syndrome related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection whose epidemiology is not very well known at present. The objective of the study was to better understand the incidence of MIS-C in the Apulia region in southern Italy. Our primary goal was to estimate the incidence of newly identified cases of MIS-C in children aged 0-18…

  • Epidemiology of Shiga Toxin-Producing Escherichia coli Infections in Southern Italy after Implementation of Symptom-Based Surveillance of Bloody Diarrhea in the Pediatric Population

    Open Access•Daniela Loconsole, Mario Giordano et al.•ARTICLE•International Journal of…•2020

    Shiga toxin-producing Escherichia coli (STEC) infections result in a significant public health impact because of the severity of the disease that, in young children especially, can lead to hemolytic-uremic syndrome (HUS). A rise in the number of HUS cases was observed in the Apulia region of Italy from 2013 to 2017, and so, in 2018, a symptom-based surveillance system for children with bloody diarrhea (BD) was initiated in order to detect and man…

No prominent works on this page.

  • Epidemiology of Shiga Toxin-Producing Escherichia coli Infections in Southern Italy after Implementation of Symptom-Based Surveillance of Bloody Diarrhea in the Pediatric Population

    Open Access•Daniela Loconsole, Mario Giordano et al.•ARTICLE•International Journal of…•2020

    Shiga toxin-producing Escherichia coli (STEC) infections result in a significant public health impact because of the severity of the disease that, in young children especially, can lead to hemolytic-uremic syndrome (HUS). A rise in the number of HUS cases was observed in the Apulia region of Italy from 2013 to 2017, and so, in 2018, a symptom-based surveillance system for children with bloody diarrhea (BD) was initiated in order to detect and man…

  • Incidence and Prevalence of Multisystem Inflammatory Syndrome in Children (MIS-C) in Southern Italy

    Open Access•Francesco La Torre, Maria Pia Elicio et al.•ARTICLE•Children•2023

    Multisystem inflammatory syndrome in children (MIS-C) is a pediatric hyperinflammatory syndrome related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection whose epidemiology is not very well known at present. The objective of the study was to better understand the incidence of MIS-C in the Apulia region in southern Italy. Our primary goal was to estimate the incidence of newly identified cases of MIS-C in children aged 0-18…

  • Unusual Onset of Hereditary Hemorrhagic Telangiectasia Due to Somatic Mutational Mosaicism

    Open Access•Virginia Mirra, Margherita Rosa et al.•ARTICLE•Children•2025

    Hereditary Hemorrhagic Telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a disorder of angiogenesis characterized by mucocutaneous telangiectasias and visceral arteriovenous malformations. This rare autosomal dominant disorder is caused by pathogenic variants in the ENG and ACVRL1 genes, and only 1-3% of case variants occur in SMAD4 . HHT clinical manifestations include telangiectasias, epistaxis, and arteriovenous malformations …

  • Animal-Assisted Psychoeducational Intervention in Paediatric Oncohaematology

    Open Access•Chiara Battaglini, Valentina Isaja et al.•ARTICLE•Children•2026

    Background : Hospitalisation for paediatric oncohaematological diseases entails significant physical and psychological stress, often compromising children's emotional regulation and daily functioning. In this context, complementary interventions can provide additional support to the clinical work conducted with children and adolescents undergoing treatment, fostering emotional awareness and well-being. This study evaluates the feasibility and per…

  • Anomalous Coronary Artery Origin from Pulmonary Artery and Coronary Fistulas

    Open Access•Mario Giordano, Martina Evangelista et al.•ARTICLE•Children•2026

    Anomalous coronary artery origin from pulmonary artery and coronary-pulmonary fistulas are the major causes of ischemic cardiopathy in children. Both anomalies are characterized by a connection between a higher and a lower pressure chamber causing coronary steal. However, several mechanisms and associated lesions may be responsible of the different presentations of the "coronary steal phenomenon". The aim of this review is to highlight the differ…

Coronary Artery Anomalies (2 works) · Epidemiology (2 works) · Incidence (geometry (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Mucocutaneous zone (2 works) · Pediatrics (2 works) · Vascular Anomalies and Treatments (2 works) · ACVRL1 (1 work) · Anxiety (1 work)

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