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Published in 2019 at "Pediatric Cardiology"
DOI: 10.1007/s00246-019-02234-9
Abstract: Severe atrioventricular valve (AVV) or semilunar valve (SLV) regurgitation in the setting of a single ventricle physiology may proceed to valve replacement if repair strategies fail. Outcome data for these children are limited. We present… read more here.
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Published in 2019 at "International journal of pediatric otorhinolaryngology"
DOI: 10.1016/j.ijporl.2019.109808
Abstract: OBJECTIVES Children with single sided deafness (SSD) show a poorer performance at school, which is attributable to reduced speech discrimination in noise, to reduced localization ability, and to a decreased power of concentration due to… read more here.
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Published in 2020 at "Progress in Pediatric Cardiology"
DOI: 10.1016/j.ppedcard.2020.101297
Abstract: Abstract Objectives Congenital heart defects (CHD) can be detected during routine antenatal scans or go undiagnosed until birth. Parents of children with Single Ventricle CHD (SVCHD) have a complex experience. This study aimed to explore… read more here.
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Published in 2017 at "Scientific Reports"
DOI: 10.1038/s41598-017-17129-z
Abstract: Early treatment of single sided deafness in children has been recommended to protect from neurodevelopmental preference for the better hearing ear and from social and educational deficits. A fairly homogeneous group of five young children… read more here.
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Published in 2022 at "Ear and Hearing"
DOI: 10.1097/aud.0000000000001204
Abstract: More children with single-sided deafness (SSD) are receiving cochlear implants (CIs) due to the expansion of CI indications. This unique group of pediatric patients has different needs than the typical recipient with bilateral deafness and… read more here.
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Published in 2021 at "Journal of Pediatric Gastroenterology and Nutrition"
DOI: 10.1097/mpg.0000000000003066
Abstract: ABSTRACT Objectives: Esophageal squamous papilloma (ESP) is a rare epithelial lesion most commonly seen in adults, with an unclear etiology and limited pediatric data available. The aim of this study was to provide an estimated… read more here.
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Published in 2023 at "International Journal of Dermatology"
DOI: 10.1111/ijd.16612
Abstract: Mastocytosis is a heterogeneous group of rare disorders characterized by the accumulation of clonal mast cells in organs such as the skin and bone marrow. The diagnosis of cutaneous mastocytosis (CM) is based on clinical… read more here.
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Published in 2017 at "Journal of Cutaneous Medicine and Surgery"
DOI: 10.1177/1203475417708163
Abstract: Background: Neurofibromatosis type 1 (NF1) is a neurocutaneous disorder caused by loss-of-function mutation in the NF1 gene. Segmental or mosaic NF1 (MNF) is an uncommon presentation of the NF1 result of postzygotic mutations that present… read more here.
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Published in 2022 at "Brain Sciences"
DOI: 10.3390/brainsci12040423
Abstract: In children, single-sided deafness (SSD) affects the development of linguistic and social skills and can impede educational progress. These difficulties may relate to cortical changes that occur following SSD, such as reduced inter-hemispheric functional asymmetry… read more here.
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Published in 2022 at "Diagnostics"
DOI: 10.3390/diagnostics12112745
Abstract: Background: Craniopharyngioma (CP) is a rare brain tumor involving the sellar region. The best management is still debated. Gross total resection (GTR) is considered the best option to improve recurrence-free survival, but considerable long-term sequelae… read more here.