The development and pilot testing of the OroFacial Awakening Symptoms Questionnaire (OFASQ). [PDF]
Saracutu OI+5 more
europepmc +1 more source
Investigating the Prevalence and Level of Pain Experienced by Australian Farmers. [PDF]
Koralegedera I+3 more
europepmc +1 more source
Investigating assessment standards and fixed passing marks in dental undergraduate finals: a mixed-methods approach. [PDF]
Ho TK, O'Malley L, Roudsari RV.
europepmc +1 more source
Development and Validation of a Questionnaire to Measure Feeding Challenges and Nutritional Problems Associated With Long-Term Enteral Nutrition Among Children With Disabilities. [PDF]
Zaher S, Ajabnoor SM.
europepmc +1 more source
A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses
ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu+10 more
wiley +1 more source
Caring perception questionnaire of the home-dwelling elderly: development and validation study. [PDF]
Feng M+7 more
europepmc +1 more source
ABSTRACT Gastrointestinal (GI) symptoms are common in patients with Williams–Beuren syndrome (WBS), but their prevalence and possible causes are not yet fully known. This study assessed GI symptoms' prevalence and their possible origin by performing a predefined set of tests in adult WBS patients.
Maria Francesca Bedeschi+10 more
wiley +1 more source
Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence
ABSTRACT The NatA N‐terminal acetyltransferase complex is composed of the NAA10 catalytic subunit and the auxiliary subunits NAA15 and HYPK. While those with variants in the enzymatic subunit develop Ogden Syndrome, individuals with variants in the NAA15 coding region develop NAA15‐related neurodevelopmental syndrome, which presents with a wide array ...
Rikhil Makwana+5 more
wiley +1 more source
ABSTRACT Individuals with an extra X or Y chromosome (sex chromosome trisomy or SCT) have an increased risk for symptoms of psychopathology and neurocognitive dysfunction. In this study, we evaluated the contribution of family history (FH) of neuropsychiatric or neurocognitive disorders to the phenotype of SCT. One hundred and six children with SCT and
Sophie van Rijn+2 more
wiley +1 more source