Results 241 to 250 of about 330,299 (301)

A Systematic Review of Adverse Childhood Experiences and Epigenetic Age Acceleration in Later Adult Life Measured With Second and Third‐Generation Epigenetic Clocks

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT We examined the relationship between adverse childhood experiences (ACEs) and epigenetic age acceleration (EAA) in adulthood as measured by second and third generation epigenetic clocks by performing a systematic review of the literature. The electronic databases MEDLINE and EMBASE were searched on 17 July 2023.
Matthew Green, Laura Horsfall, Azam Saied   +2 more
wiley   +1 more source

Application of a 3D printed wig protection device after decompressive craniectomy. [PDF]

Sci Rep
Ma S, Li C, Gu Y, Chen Y, Li X, Wang Q, Xu H.   +6 more
europepmc   +1 more source

Psychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.
Julia M. Morales, Camille F. Villar, Beatriz Varman, Gianna M. Colombo, Danqi Li, Sarah J. Sadek, Marie‐Eve Robinson, Chaya N. Murali, Kara Ayers, Jocelyn Gomez, Brendan Lee, V. Reid Sutton, Eric A. Storch, Andrew D. Wiese   +13 more
wiley   +1 more source

Actical Accelerometers as a Clinical Tool for the Monitoring of Sleeping and Resting Periods in Individual Dogs. [PDF]

Animals (Basel)
Straube-Koegler S, Dobenecker B, Lauer S, Wielaender F, Zablotski Y, Fischer A.   +5 more
europepmc   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source

Monitoring respiratory mechanics as a training tool for manual ventilation. [PDF]

Front Pediatr
Carlomagno CEB, Mascaretti RS, Lyra JC, Zacharias RSB, Magalhaes M, Breuel PAF, Rebello CM.   +6 more
europepmc   +1 more source

Gemini Surfactants: Advances in Applications and Prospects for the Future. [PDF]

Molecules
Kowalczyk I, Szulc A, Brycki B.
europepmc   +1 more source

Chronically implantable μLED arrays for optogenetic cortical surface stimulation in mice. [PDF]

Nat Commun
Greer R, Verdier A, Butt E, Cheng Y, Callas E, McAlinden N, Aniorte A, Mabrouk Kakaouia E, Pereyra M, Dawson MD, Bathellier B, Mathieson K.   +11 more
europepmc   +1 more source

A Simple and Cost-Effective Retractor for Transorbital Neurosurgery: Technical Note and Application in Lacrimal Keyhole Approaches. [PDF]

J Clin Med
Ferlendis L, Fava A, Passeri T, Abbritti R, Froelich S.   +4 more
europepmc   +1 more source