Atrophin 1-Related CHEDDA Syndrome Associated with Different Inheritance and Epileptic Encephalopathy with Hand Stereotypies. [PDF]
Özkale Y +3 more
europepmc +1 more source
‘We Teach Kids About It So They Don't Get Addicted’: Gender, Porn and Sex Education in New Zealand
ABSTRACT This research sought to explore young people's and teachers' understandings of porn. Drawing on a qualitative content analysis of small focus group interview data with 106 young people aged 12–16 years old and semi‐structured interviews with six teachers in Aotearoa, New Zealand, I examine their perceptions of porn and the place of porn in sex
Claire Meehan
wiley +1 more source
Benign Movement Disorders Mimicking Seizures in Children: A Retrospective Cohort Study. [PDF]
Eroglu A.
europepmc +1 more source
Summary Chronic stress, characterized by increased long‐term exposure to the glucocorticoid hormone cortisol, is increasingly linked to obesity development. Still, various knowledge gaps persist, including on underlying pathophysiological mechanisms. The aim of the current review is to provide the latest insights on the connection between stress and ...
Robin Lengton +4 more
wiley +1 more source
Neurological findings in a cohort of adults with down syndrome. [PDF]
Grotteschi N +11 more
europepmc +1 more source
Polyamine metabolism is innervation responsive and involved in denervation‐induced muscle atrophy. Inhibition of polyamine metabolism attenuates muscle atrophy by restraining proteolysis and preserving MuSCs homeostasis. Denervation‐induced activation of FAP‐derived FGF7 drives premature MuSCs activation, while DFMO suppresses this paracrine cue to ...
Mingming Zhang +9 more
wiley +1 more source
During development, the oxygen‐sensitive transcription factor Zeb2 restrains astrocyte proliferation and maturation to ensure balanced retinal angiogenesis. In disease, it promotes the neurotoxic A1 astrocyte phenotype and inflammation, thereby promoting reparative revascularization over pathological neovascularization.
Jing Liu +5 more
wiley +1 more source
Mixed Movement Disorder Caused by <i>ADCY5</i> Pathogenic Variant Successfully Treated With Caffeine: A Case From Ukraine. [PDF]
Tsoma E +7 more
europepmc +1 more source
Precision therapies for rare childhood neurogenetic movement disorders
Genetic childhood movement disorders are a heterogeneous group of individually rare conditions that cause abnormal movements such as dystonia, chorea, myoclonus, tremor, and parkinsonism.
Spaull, Robert
core
Translation and Validation of the Arabic Version of the Revised Restrictive Behaviours Scale Among Iraqi Children With Autism Spectrum Disorder: A Suggestion for Model Modification. [PDF]
Hussein Al-Sultan RR +6 more
europepmc +1 more source

