Results 181 to 190 of about 138,344 (267)

The Need for Flexible, Co-Developed Adverse Childhood Experiences Assessment: Response to Chang and Su: "Adverse Childhood Experiences in the Digital Era: An Urgent Call for Precision Assessment&quot.

Psychother Psychosom
Caes L, Christogianni A, Hales TG, Colvin LA.   +3 more
europepmc   +1 more source

Students' perceptions on determinants of cyberbullying at a rural higher education institution in Limpopo. [PDF]

BMC Public Health
Nkuna N, Baloyi V.
europepmc   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu, Rosan Kenana, Rana Chakrabarti, Sarah D. P. Wilhelm, Joseph Andrews, Susan J. Leat, Christina Parker, Michael Miller, Leslie A. Nangle, Wendy McCaul, Ashfia Chowdhury, Natalie Hutchings, Ryan A. Adams, Lauren Guy, Mandy Rhody, Verena Juncal, Marisa I. Mendes, Desiree E. C. Smith, Gajja S. Salomons, Angelica A. Moresco, Daphne L. McCulloch, D. Holmes Morton, Ilka U. Heinemann, C. Anthony Rupar   +23 more
wiley   +1 more source

Developmental literacy and epistemic dignity as primary child protection: a developmentally staged, disability-inclusive public-health framework for preventing adverse childhood experiences. [PDF]

Front Public Health
Niederlohmann E.
europepmc   +1 more source

Authors' reply to: Todd et al., prenatal and intrapartum antibiotic exposure and childhood infections: considerations and complexities. [PDF]

Lancet Reg Health Am
Coggins SA, Mukhopadhyay S.
europepmc   +1 more source

Childhood by Design: Toys and the Material Culture of Childhood

Le magasin des enfants, 2016
openaire   +2 more sources

A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco, Aaron Williams, Claudia Soler‐Alfonso, Emily Waskow, Elizabeth Mizerik, Fernando Scaglia, Chaya N. Murali   +6 more
wiley   +1 more source

Clinical Signs Associated With Mortality and Sepsis in Young Infants: A Systematic Review and Meta-Analysis. [PDF]

JAMA Pediatr
Driker S, Mathias S, Fung A, Widyaningsih SA, Schmeck N, Adnan J, Kim Y, Hussaini AS, Kehoe T, North K, Hoey A, Shafiq Y, Wade CG, Mediratta RP, Rees CA, Lee AC.   +15 more
europepmc   +1 more source

Immune Modulatory Therapy for Severe Dengue Hemorrhagic Fever in a Patient With Mitochondrial Complex I Deficiency: A Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Dengue virus (DENV) poses a serious global health challenge, particularly in cases of dengue hemorrhagic fever (DHF). Patients with preexisting mitochondrial disorders may be at increased risk for complications due to the specific impact of DENV on mitochondrial‐dependent cellular processes and immune function.
Audra N. Iness, Ameya S. Walimbe, Emily R. Strouphauer, Michio Hirano, Alejandro D. Iglesias, Valentina Emmanuele, Caitlin C. Griffin, Sheldon L. Kaplan, William A. Gomes, Karen K. Moeller, Stephen F. Kralik, Fernando Scaglia   +11 more
wiley   +1 more source

Actinomyces graevenitzii Detected in a Case of Endobronchial Actinomycosis Caused by Foreign Body Aspiration: A Case Report. [PDF]

Cureus
Hakamada N, Odaka H, Shimada K, Hatakeyama N, Tokairin T.   +4 more
europepmc   +1 more source