Search Results - "Lonardo, Maria Concetta"
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Incomplete Kawasaki Disease with Peripheral Facial Nerve Palsy and Lung Nodules: A Case Report and Literature Review
Published in Children (Basel) (01-04-2023)“…The diagnosis of Kawasaki disease (KD) is challenging and often delayed mainly in case of young infants and in presence of an incomplete disease and atypical…”
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A rare case of hydrometrocolpos from persistent urogenital sinus in patient affected by adrenogenital syndrome
Published in Journal of ultrasound (01-09-2018)“…Persistent urogenital sinus (PUGS) is a congenital pathological condition characterized by an abnormal communication between the urethra and vagina, which has…”
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Severe Myopia with Unusual Retinal Anomalies and Dandy-Walker Sequence in Two Sibs. A Distinct New Neuro-ocular Disorder
Published in Ophthalmic genetics (01-12-2013)“…Abstract We have observed a male and a female, sibs of non-consanguineous parents, affected by severe myopia with characteristic retinal defects and…”
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A case of polimalformed fetus with a microdeletion of CTNNA3 gene
Published in Journal of prenatal medicine (01-07-2016)“…We report a case of a male fetus of 20 weeks of gestation with plurimalformed observed by transonic scan and confirmed by MR. The karyotype was 46, XY…”
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Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences
Published in Journal of prenatal medicine (01-07-2014)“…the purpose of this paper is to report the first case of megaurethra in a fetus with Meckel syndrome and in a fetus with femal pseudoermaphroditism. the former…”
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Pediatric Minimal Change Disease and AKI following the Pfizer-BioNTech COVID-19 Vaccine: causal or incidental correlation?
Published in Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia (21-12-2022)“…The global coronavirus 2019 (COVID-19) pandemic required vaccination even in children to reduce infection. We report on the development of acute kidney injury…”
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A case of polimalformed fetus with a microdeletion of CTNNA3 gene
Published in Journal of prenatal medicine (01-07-2016)Get full text
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Severe Myopia with Unusual Retinal Anomalies and Dandy-Walker Sequence in Two Sibs. A Distinct New Neuro-ocular Disorder
Published in Ophthalmic Genetics (01-12-2013)“…We have observed a male and a female, sibs of non-consanguineous parents, affected by severe myopia with characteristic retinal defects and Dandy-Walker…”
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Report -
10
Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences
Published in Journal of prenatal medicine (01-04-2014)“…OBJECTIVEthe purpose of this paper is to report the first case of megaurethra in a fetus with Meckel syndrome and in a fetus with femal pseudoermaphroditism…”
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