Participation in Daily Activities of Children with Atopic Diseases and Its Relation to Their Sensory Modulation Difficulties.

(1) Background: Participation in daily activities is critical for a child's health, development and wellbeing and is considered a main outcome measure of intervention efficiency. Atopic diseases affect children's daily life and routines but the knowledge about impacts on participation is limited. (2) Objectives: a.

Heterozygous de novo variants in cause hypomyelinating leukodystrophy through impaired HSP60 oligomerisation.

Introduction: Hypomyelinating leukodystrophies are a group of genetic disorders, characterised by severe permanent myelin deficiency. Their clinical features include developmental delay with or without neuroregression, nystagmus, central hypotonia, progressing to spasticity and ataxia. encodes the HSP60 chaperonin protein, mediating ATP-dependent folding of imported proteins in the mitochondrial matrix.

Semi-Opaque Perovskite Solar Cells.

Transparent photovoltaics are garnering significant interest for power generation in applications where light transmission is required. Metal halide perovskites have emerged as one of the most lucrative material classes for such device architectures due to their exceptional optoelectronic properties, and compositional versatility enabling a wide range of transparency levels. While research has primarily focused on semitransparent solar cell architectures, their colored appearance, and efficiency limitations hinder their practical applicability.

-Related Autosomal Recessive Retinitis Pigmentosa with Intellectual Disability: Confirming and Extending the Phenotypic Spectrum and Bioinformatics Analyses.

Mutations in the gene (S phase Cyclin A-Associated Protein residing in the Endoplasmic Reticulum) have recently been associated with retinitis pigmentosa (RP) and intellectual disability (ID). In 2011, a possible involvement of in human diseases was discovered for the first time due to the identification of a homozygous mutation causing ID in an Iranian family. Later, five studies were published in 2019 that described patients with autosomal recessive syndromic retinitis pigmentosa (arRP) accompanied by ID and attention-deficit/hyperactivity disorder (ADHD).