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Flavia Indrio

Biographic Data

ID7597920
NAMEFlavia Indrio
GIVEN NAMESFlavia
FAMILY NAMEIndrio
SIGNATUREINDRIO F
AFFILIATIONSUniversity of Foggia
ORCID0000-0001-9789-7878
VERIFIEDYes
TOTAL WORKS5
TOTAL CITATIONS0
AUTHOR COUNT5
EDITOR COUNT0
FIRST PUBLICATION YEAR2017
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Non-Traumatic Clavicular Lesions in Children

    Open Access•Federico Diomeda, Rossella Greco et al.•ARTICLE•Children•2026

    CNO predominates among pediatric non-traumatic clavicular lesions, but LCH and rare conditions are not uncommon, underscoring the need for careful differential diagnosis and targeted imaging

  • New Trigger for Stroke-like Episode in Sturge–Weber Syndrome

    Open Access•Emiliano Altavilla, Andrea De Giacomo et al.•ARTICLE•Children•2025

    Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…

  • Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome

    Open Access•Pierluigi Zaza, Flavia Indrio et al.•ARTICLE•Children•2022

    Loeys-Dietz syndrome (LDS) is a rare autosomal-dominant disorder of the connective tissue with some typical vascular findings, skeletal manifestations, craniofacial features, and cutaneous findings with a wide phenotypic spectrum. Six different genes are involved in LDS and the diagnosis is based on the identification of a heterozygous pathogenic variant in TGFBR1 , TGFBR2 , SMAD3 , TGFB2 , TGFB3 , or SMAD2 in children with suggestive findings. T…

  • Specific Learning Disorders and Special Educational Needs during Covid-19 Pandemic; Pilot Survey Study Performed in Local District Schools in Italy

    Open Access•Flavia Marchese, Assunta Grillo et al.•ARTICLE•Children•2022

    The findings of this pilot study suggest that distance learning programs are able to achieve adequate educational goals, despite the difficulties of the lockdown period

  • Complementary Feeding

    Open Access•Mary Fewtrell, Jiri Bronsky et al.•ARTICLE•Journal of Pediatric Gastroenterolo…•2017

    This position paper considers different aspects of complementary feeding (CF), focussing on healthy term infants in Europe. After reviewing current knowledge and practices, we have formulated these recommendations: Timing : Exclusive or full breast‐feeding should be promoted for at least 4 months (17 weeks, beginning of the 5th month of life) and exclusive or predominant breast‐feeding for approximately 6 months (26 weeks, beginning of the 7th mo…

No prominent works on this page.

  • Complementary Feeding

    Open Access•Mary Fewtrell, Jiri Bronsky et al.•ARTICLE•Journal of Pediatric Gastroenterolo…•2017

    This position paper considers different aspects of complementary feeding (CF), focussing on healthy term infants in Europe. After reviewing current knowledge and practices, we have formulated these recommendations: Timing : Exclusive or full breast‐feeding should be promoted for at least 4 months (17 weeks, beginning of the 5th month of life) and exclusive or predominant breast‐feeding for approximately 6 months (26 weeks, beginning of the 7th mo…

  • Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome

    Open Access•Pierluigi Zaza, Flavia Indrio et al.•ARTICLE•Children•2022

    Loeys-Dietz syndrome (LDS) is a rare autosomal-dominant disorder of the connective tissue with some typical vascular findings, skeletal manifestations, craniofacial features, and cutaneous findings with a wide phenotypic spectrum. Six different genes are involved in LDS and the diagnosis is based on the identification of a heterozygous pathogenic variant in TGFBR1 , TGFBR2 , SMAD3 , TGFB2 , TGFB3 , or SMAD2 in children with suggestive findings. T…

  • Specific Learning Disorders and Special Educational Needs during Covid-19 Pandemic; Pilot Survey Study Performed in Local District Schools in Italy

    Open Access•Flavia Marchese, Assunta Grillo et al.•ARTICLE•Children•2022

    The findings of this pilot study suggest that distance learning programs are able to achieve adequate educational goals, despite the difficulties of the lockdown period

  • New Trigger for Stroke-like Episode in Sturge–Weber Syndrome

    Open Access•Emiliano Altavilla, Andrea De Giacomo et al.•ARTICLE•Children•2025

    Background . Sturge-Weber syndrome (SWS) is a rare non-hereditary neurovascular disorder characterized by capillary-venous malformations on the face, ocular vascular anomalies, and leptomeningeal capillary-venous malformations. Patients with SWS often experience cerebral perfusion impairment, increasing their risk for stroke-like episodes, seizures, and motor and cognitive impairments. Methods . We report the case of a 2-year-old boy diagnosed wi…

  • Non-Traumatic Clavicular Lesions in Children

    Open Access•Federico Diomeda, Rossella Greco et al.•ARTICLE•Children•2026

    CNO predominates among pediatric non-traumatic clavicular lesions, but LCH and rare conditions are not uncommon, underscoring the need for careful differential diagnosis and targeted imaging

Medicine (4 works) · Family medicine (2 works) · Pediatrics (2 works) · Anesthesia (1 works) · Bone and Dental Protein Studies (1 works) · Breastfeeding Practices and Influences (1 works) · Cardiovascular Issues in Pregnancy (1 works) · Celiac Disease Research and Management (1 works) · Child Development and Digital Technology (1 works) · Clavicle (1 works)

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