Results 21 to 30 of about 423,878 (284)

Transient Elastography for Detection of Liver Fibrosis in Children With Autosomal Recessive Polycystic Kidney Disease

open access: yesFrontiers in Pediatrics, 2019
Introduction: Congenital hepatic fibrosis (CHF) is invariably present in all patients with autosomal recessive polycystic kidney disease (ARPKD) but is usually clinically asymptomatic.
Dorota Wicher   +8 more
doaj   +1 more source

Symptom Scores and pH-Impedance: Secondary Analysis of a Randomized Controlled Trial in Infants Treated for Gastroesophageal Reflux

open access: yesGastro Hep Advances, 2022
Background and Aims: To evaluate and compare gastroesophageal reflux (GER) symptom scores with pH-impedance and test the effects of acid-suppressive medications with or without feeding modifications on pH-impedance in high-risk infants.
Zakia Sultana   +7 more
doaj   +1 more source

Clinical identification of feeding and swallowing disorders in 0-6 month old infants with Down syndrome [PDF]

open access: yes, 2019
Feeding and swallowing disorders have been described in children with a variety of neurodevelopmental disabilities, including Down syndrome (DS). Abnormal feeding and swallowing can be associated with serious sequelae such as failure to thrive and ...
Bull, Marilyn J.   +10 more
core   +1 more source

Cationic Polystyrene Resolves Nonalcoholic Steatohepatitis, Obesity, and Metabolic Disorders by Promoting Eubiosis of Gut Microbiota and Decreasing Endotoxemia. [PDF]

open access: yes, 2017
A pandemic of metabolic diseases, consisting of type 2 diabetes, nonalcoholic fatty liver disease, and obesity, has imposed critical challenges for societies worldwide, prompting investigation of underlying mechanisms and exploration of low-cost and ...
Bai, Li   +22 more
core   +1 more source

A service evaluation of parent adherence with dysphagia management therapy guidelines: Reports from family carers supporting children with complex needs in Greece [PDF]

open access: yes, 2020
Purpose: Many children with complex needs exhibit eating, drinking and/or swallowing disorders (dysphagia). These children often have associated learning needs, and require assistance from carers for daily tasks such as eating and drinking.
Alexia Charpentier   +5 more
core   +1 more source

Targeted Next-Generation Sequencing in Diagnostic Approach to Monogenic Cholestatic Liver Disorders—Single-Center Experience

open access: yesFrontiers in Pediatrics, 2020
Objective: To evaluate the clinical utility of panel-based NGS in the diagnostic approach of monogenic cholestatic liver diseases.Study design: Patients with diagnosis of chronic cholestatic liver disease of an unknown etiology underwent NGS of targeted ...
Patryk Lipiński   +11 more
doaj   +1 more source

From autism to eating disorders and more: the role of oxytocin in neuropsychiatric disorders [PDF]

open access: yes, 2016
Oxytocin (oxy) is a pituitary neuropeptide hormone synthesized from the paraventricular and supraoptic nuclei within the hypothalamus. Like other neuropeptides, oxy can modulate a wide range of neurotransmitter and neuromodulator activities. Additionally,
Di Bonaventura, Maria Vittoria Micioni   +3 more
core   +2 more sources

Mechanisms of bradycardia in premature infants: Aerodigestive–cardiac regulatory–rhythm interactions

open access: yesPhysiological Reports, 2020
Objective Eating difficulties coupled with cardiorespiratory spells delay acquisition of feeding milestones in convalescing neonates, and the mechanisms are unclear.
Kathryn A. Hasenstab‐Kenney   +5 more
doaj   +1 more source

Adult avoidant/restrictive food intake disorder: a case report [PDF]

open access: yesJornal Brasileiro de Psiquiatria, 2020
The aim this report is to present an adult case of avoidant/restrictive food intake disorder (ARFID) in a patient with atypical development. To emphasize the diagnostic and behavioral characteristics of this new nosological category included in the ...
Evelin Mascarenhas Soffritti   +4 more
doaj   +1 more source

DCDC2-Related Ciliopathy: Report of Six Polish Patients, Novel DCDC2 Variant, and Literature Review of Reported Cases

open access: yesDiagnostics, 2023
Introduction: The increasing usage of NGS technology has enabled the discovery of new causal genes in ciliopathies, including the DCDC2 gene. The aim of our study was to present the clinical, pathological and molecular report of six patients (from three ...
Patryk Lipiński   +8 more
doaj   +1 more source

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