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  1. Article ; Online: Lumbar spine epidural abscess and facet joint septic arthritis in a pediatric patient.

    Vergine, Gianluca / Ferrè, Cristina / Menetti, Federico / Libertucci, Francesca / Tonti, Giacomo / Pedini, Annalisa / Poloni, Maurizio

    Pediatrics and neonatology

    2023  Volume 64, Issue 4, Page(s) 474–475

    MeSH term(s) Humans ; Child ; Epidural Abscess/complications ; Epidural Abscess/diagnostic imaging ; Zygapophyseal Joint/diagnostic imaging ; Spine ; Arthritis, Infectious/diagnosis ; Magnetic Resonance Imaging ; Staphylococcal Infections/complications ; Staphylococcal Infections/diagnosis
    Language English
    Publishing date 2023-01-26
    Publishing country Singapore
    Document type Journal Article
    ZDB-ID 2441816-X
    ISSN 2212-1692 ; 1875-9572
    ISSN (online) 2212-1692
    ISSN 1875-9572
    DOI 10.1016/j.pedneo.2022.12.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Bartter Syndrome Type 1 Presenting as Nephrogenic Diabetes Insipidus.

    Vergine, Gianluca / Fabbri, Elena / Pedini, Annalisa / Tedeschi, Silvana / Borsa, Niccolò

    Case reports in pediatrics

    2018  Volume 2018, Page(s) 9175271

    Abstract: Bartter syndrome (BS) type 1 (OMIM #601678) is a hereditary salt-losing renal tubular disorder characterized by hypokalemic metabolic alkalosis, hypercalciuria, nephrocalcinosis, polyuria, recurrent vomiting, and growth retardation. It is caused by loss- ... ...

    Abstract Bartter syndrome (BS) type 1 (OMIM #601678) is a hereditary salt-losing renal tubular disorder characterized by hypokalemic metabolic alkalosis, hypercalciuria, nephrocalcinosis, polyuria, recurrent vomiting, and growth retardation. It is caused by loss-of-function mutations of the
    Language English
    Publishing date 2018-02-21
    Publishing country United States
    Document type Case Reports
    ZDB-ID 2659094-3
    ISSN 2090-6811 ; 2090-6803
    ISSN (online) 2090-6811
    ISSN 2090-6803
    DOI 10.1155/2018/9175271
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Patent ductus arteriosus in preterm infants born before 30 weeks' gestation: high rate of spontaneous closure after hospital discharge.

    Romagnoli, Vittorio / Pedini, Annalisa / Santoni, Monica / Scutti, Grazia / Colaneri, Massimo / Pozzi, Marco / Cogo, Paola E / Carnielli, Virgilio P

    Cardiology in the young

    2018  Volume 28, Issue 8, Page(s) 995–1000

    Abstract: AimThe aim of this study was to determine the spontaneous closure rate of patent ductus arteriosus at a 2-year follow-up, following failed medical therapy and beyond initial hospital discharge, and to evaluate in-hospital spontaneous or pharmacological ... ...

    Abstract AimThe aim of this study was to determine the spontaneous closure rate of patent ductus arteriosus at a 2-year follow-up, following failed medical therapy and beyond initial hospital discharge, and to evaluate in-hospital spontaneous or pharmacological closure rates.Materials and methodsA retrospective evaluation was conducted in a cohort of preterm infants admitted to the Neonatal ICU of Ancona between January, 2004 and June, 2013. Inclusion criteria were gestational age between 24+0 and 29+6 weeks or birth weight 1.5 mm, a left atrium-to-aorta ratio >1.4, and/or reversal of end-diastolic flow in the aorta >30% of the anterograde. First-line treatment was intravenous ibuprofen. Intravenous indomethacin was used if ibuprofen failed. Surgical ligation was considered in haemodynamically significant patent ductus arteriosus after medical treatment.
    Results: A total of 593 infants met the inclusion criteria, and patent ductus arteriosus was diagnosed in 317 (53.4%). Among them, 283 (89.3%) infants had haemodynamically significant patent ductus arteriosus, with pharmacological closure achieved in 228 (80.6%) infants and surgical ligation performed in 20 (7.1%). Follow-up at 24 months was available for 39 (81.3%) of 48 infants with patent ductus arteriosus at the hospital discharge: 36 (92.3%) underwent spontaneous closure, two (5.1%) underwent surgical ligation, and one (2.6%) had a patent ductus arteriosus.DiscussionA significant number of patent ductus arteriosus that fail pharmacological closure undergo spontaneous closure by the age of 2 years. This information should be taken into account when considering surgery or additional attempts of pharmacological closure.
    MeSH term(s) Administration, Intravenous ; Cyclooxygenase Inhibitors/therapeutic use ; Ductus Arteriosus, Patent/therapy ; Female ; Follow-Up Studies ; Gestational Age ; Humans ; Ibuprofen/therapeutic use ; Indomethacin/therapeutic use ; Infant ; Infant, Extremely Low Birth Weight ; Infant, Extremely Premature ; Infant, Newborn ; Italy/epidemiology ; Ligation ; Male ; Patient Discharge ; Remission Induction ; Remission, Spontaneous ; Retrospective Studies
    Chemical Substances Cyclooxygenase Inhibitors ; Ibuprofen (WK2XYI10QM) ; Indomethacin (XXE1CET956)
    Language English
    Publishing date 2018-06-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 1078466-4
    ISSN 1467-1107 ; 1047-9511
    ISSN (online) 1467-1107
    ISSN 1047-9511
    DOI 10.1017/S1047951118000641
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 4050: Show issues Location:
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  4. Article ; Online: A case of syndromic neutropenia and mutation in G6PC3.

    Gatti, Simona / Boztug, Kaan / Pedini, Annalisa / Pasqualini, Claudia / Albano, Veronica / Klein, Christoph / Pierani, Paolo

    Journal of pediatric hematology/oncology

    2011  Volume 33, Issue 2, Page(s) 138–140

    Abstract: Background: A previously unrecognized syndrome with congenital neutropenia and various organ abnormalities has been described recently, caused by mutations in the gene encoding glucose-6-phosphatase, catalytic subunit 3 (G6PC3).: Observation: A 10- ... ...

    Abstract Background: A previously unrecognized syndrome with congenital neutropenia and various organ abnormalities has been described recently, caused by mutations in the gene encoding glucose-6-phosphatase, catalytic subunit 3 (G6PC3).
    Observation: A 10-year-old boy from Ecuador suffering from severe neutropenia and multiple nonhematopoietic abnormalities was admitted to our department. We identified a novel mutation in the G6PC3 gene (c. 765_delAG; p.S255fs).
    Conclusions: This is the first case of G6PC3 deficiency in a patient from South America, caused by a novel mutation in the G6PC3 gene. Our results give insights into the molecular and clinical variability of this disease.
    MeSH term(s) Abnormalities, Multiple/genetics ; Abnormalities, Multiple/pathology ; Cell Differentiation ; Child ; Glucose-6-Phosphatase/genetics ; Humans ; Male ; Mutation ; Neutropenia/complications ; Neutropenia/congenital ; Neutropenia/genetics ; Neutropenia/pathology ; Syndrome
    Chemical Substances Glucose-6-Phosphatase (EC 3.1.3.9) ; G6PC3 protein, human (EC 3.1.3.9.)
    Language English
    Publishing date 2011-03
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 1231152-2
    ISSN 1536-3678 ; 1077-4114 ; 0192-8562
    ISSN (online) 1536-3678
    ISSN 1077-4114 ; 0192-8562
    DOI 10.1097/MPH.0b013e3181f46bf4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Efficacy of propranolol treatment in thyroid dysfunction associated with severe infantile hepatic hemangioma.

    Vergine, Gianluca / Marsciani, Alberto / Pedini, Annalisa / Brocchi, Silvia / Marsciani, Martino / Desiderio, Elena / Bertelli, Sara / Vecchi, Vico

    Hormone research in paediatrics

    2012  Volume 78, Issue 4, Page(s) 256–260

    Abstract: Infantile hepatic hemangioma can be associated to consumptive hypothyroidism due to overexpression of type 3 deiodinase in the endothelium of vascular tumor, which catalyzes the conversion of T4 to reverse T3 (rT3) and of T3 to T2, both of which are ... ...

    Abstract Infantile hepatic hemangioma can be associated to consumptive hypothyroidism due to overexpression of type 3 deiodinase in the endothelium of vascular tumor, which catalyzes the conversion of T4 to reverse T3 (rT3) and of T3 to T2, both of which are biologically inactive. Here, we report an infant with a massive biopsy-proven infantile hepatic hemangioma who developed thyroid dysfunction without a typical biochemical profile consistent with severe consumptive hypothyroidism, despite the large tumor burden. Our patient was treated with propranolol that rapidly resolved both hepatic hemangioma and thyroid dysfunction. We propose propranolol as a first-line therapy of thyroid dysfunction associated with infantile hepatic hemangioma, in order to avoid interference with neurological development caused by hypothyroidism in the first months of life.
    MeSH term(s) Adrenergic beta-Antagonists/therapeutic use ; Female ; Hemangioma/complications ; Hemangioma/drug therapy ; Humans ; Infant ; Liver Neoplasms/complications ; Liver Neoplasms/drug therapy ; Propranolol/therapeutic use ; Severity of Illness Index ; Thyroid Diseases/complications ; Thyroid Diseases/drug therapy ; Treatment Outcome
    Chemical Substances Adrenergic beta-Antagonists ; Propranolol (9Y8NXQ24VQ)
    Language English
    Publishing date 2012
    Publishing country Switzerland
    Document type Case Reports ; Journal Article
    ZDB-ID 2537278-6
    ISSN 1663-2826 ; 1663-2818
    ISSN (online) 1663-2826
    ISSN 1663-2818
    DOI 10.1159/000337253
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Efficacy of Propranolol Treatment in Thyroid Dysfunction Associated with Severe Infantile Hepatic Hemangioma

    Vergine, Gianluca / Marsciani, Alberto / Pedini, Annalisa / Brocchi, Silvia / Marsciani, Martino / Desiderio, Elena / Bertelli, Sara / Vecchi, Vico

    Hormone Research in Paediatrics

    2012  Volume 78, Issue 4, Page(s) 256–260

    Abstract: Infantile hepatic hemangioma can be associated to consumptive hypothyroidism due to overexpression of type 3 deiodinase in the endothelium of vascular tumor, which catalyzes the conversion of T4 to reverse T3 (rT3) and of T3 to T2, both of which are ... ...

    Institution Department of Pediatrics, ‘Infermi’ Hospital, Rimini Department of Pediatrics, ‘S.Orsola Malpighi’ Hospital, Bologna, and Department of Growth and Reproduction, ‘S. Anna’ Hospital, Ferrara, Italy
    Abstract Infantile hepatic hemangioma can be associated to consumptive hypothyroidism due to overexpression of type 3 deiodinase in the endothelium of vascular tumor, which catalyzes the conversion of T4 to reverse T3 (rT3) and of T3 to T2, both of which are biologically inactive. Here, we report an infant with a massive biopsy-proven infantile hepatic hemangioma who developed thyroid dysfunction without a typical biochemical profile consistent with severe consumptive hypothyroidism, despite the large tumor burden. Our patient was treated with propranolol that rapidly resolved both hepatic hemangioma and thyroid dysfunction. We propose propranolol as a first-line therapy of thyroid dysfunction associated with infantile hepatic hemangioma, in order to avoid interference with neurological development caused by hypothyroidism in the first months of life.
    Keywords Propranolol ; Hepatic hemangioma ; Thyroid dysfunction ; Iodothyronine deiodinase ; TSH-like factor
    Language English
    Publishing date 2012-08-14
    Publisher S. Karger AG
    Publishing place Basel, Switzerland
    Document type Article
    Note Novel Insights from Clinical Practice
    ZDB-ID 2537278-6
    ISSN 1663-2826 ; 1663-2818
    ISSN (online) 1663-2826
    ISSN 1663-2818
    DOI 10.1159/000337253
    Database Karger publisher's database

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