Results 41 to 50 of about 10,379 (220)

Visuomotor competencies and primary monosymptomatic nocturnal enuresis in prepubertal aged children. [PDF]

open access: yes, 2013
Background: Primary monosymptomatic nocturnal enuresis (PMNE) is a common problem in the developmental ages; it is the involuntary loss of urine during the night in children older than 5 years of age.
Carotenuto, M.   +9 more
core   +1 more source

Facial Patterns and Obstructive Sleep Apnea in Children Seeking for Orthodontic Treatment: Data From 3671 Polysomnographic Recordings

open access: yesOrthodontics &Craniofacial Research, EarlyView.
ABSTRACT Aim To evaluate the association between vertical and sagittal facial profile characteristics and the diagnosis/severity of Obstructive Sleep Apnea (OSA) based on hospital‐based polysomnography (PSG) in children attending their first orthodontic visit.
Derek Mahony   +7 more
wiley   +1 more source

Information retrieval or document retrieval? Terminological confusions and unrealistic goals in information science, exemplified in relation to generative artificial intelligence

open access: yesJournal of the Association for Information Science and Technology, Volume 77, Issue 5, Page 714-726, May 2026.
Abstract ChatGPT and related technologies have revived an old issue in information science (IS) concerning information retrieval (IR) versus document retrieval. Since 1950, the term IR has primarily been used as a misnomer for document retrieval. This problematic terminology reflects a desire to go beyond documents and provide, in response to user ...
Birger Hjørland
wiley   +1 more source

Eating and feeding disorders in pediatric age [PDF]

open access: yes, 2018
Eating and feeding disorders are common in pediatric age and may be important to discover and recover the early symptoms in order to optimize the treatment and ...
Cerroni F.   +20 more
core   +1 more source

Hypercalciuria in Children with Monosymptomatic Nocturnal Enuresis

open access: yesHaseki Tıp Bülteni, 2014
Aim: Nocturnal enuresis is a common problem in childhood. We aimed to evaluate the role of urinary calcium excretion in children with monosymptomatic nocturnal enuresis (MNE). Methods: This study included 60 children with MNE and 30 healthy controls. In
Mahmut Çivilibal   +2 more
doaj   +1 more source

Sodium fraction excretion rate in nocturnal enuresis correlates with nocturnal polyuria and osmolality [PDF]

open access: yes, 2004
: Purpose: We verify the sodium fraction excretion rate (FE Na) and potassium fraction excretion WE K) rates in monosymptomatic nocturnal enuresis. We also correlate FE Na and FE K to urinary osmolality, nocturnal polyuria and vasopressin in the same ...
Aceto, G.   +5 more
core   +1 more source

Once‐Nightly Sodium Oxybate Meets American Academy of Sleep Medicine Criteria for Treatment of Narcolepsy

open access: yesJournal of Sleep Research, Volume 35, Issue 2, April 2026.
ABSTRACT Data from the REST‐ON trial were not available before the 2021 American Academy of Sleep Medicine (AASM) clinical practice guideline update, which included a literature review through August 2020. This post hoc analysis from REST‐ON assessed participants who achieved clinically significant improvements on individual AASM clinical significance ...
Luis E. Ortiz   +7 more
wiley   +1 more source

Lasten yökastelun hoito perusterveydenhuollossa : kartoitus Etelä-Savon sairaanhoitopiirin alueella [PDF]

open access: yes, 2012
Lasten yökastelu on hyvin yleinen ongelma, Suomessa on arviolta 30 000–50 000 vähintään viisivuotiasta lasta, jotka tarvitsevat apua yökastelun hoitoon.
Vallenius, Anne
core  

Risk factors and functional abnormalities associated with adult onset secondary nocturnal enuresis in women [PDF]

open access: yes, 2015
Aims The study aims to evaluate bothersome lower urinary tract symptoms (LUTS), risk factors, and associated functional abnormalities in women reporting adult onset secondary nocturnal enuresis (SNE), to help understand factors associated with SNE ...
Abeygunasekera   +35 more
core   +2 more sources

Behavioral Phenotype and Neuropsychological Profile of an Adult With Smith‐Magenis Syndrome due to a Previously Unreported RAI1 Mutation: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Smith‐Magenis Syndrome (SMS) is an uncommon genetic disorder caused by microdeletions of chromosome 17p11.2 including the RAI1 gene, or loss‐of‐function mutations that directly affect RAI1. Due to the involvement of RAI1 in neurodevelopment, SMS leads to typical pathologic features in the behavioral and physical phenotype that must be ...
Edgar Andrés Chavarría‐Martínez   +4 more
wiley   +1 more source

Home - About - Disclaimer - Privacy