Results 291 to 300 of about 1,723,878 (343)

Cow‐Related Injuries in Wisconsin During 2017−2023

American Journal of Industrial Medicine, EarlyView.
ABSTRACT Introduction The dairy industry–a key industry for the economy–remains a potentially hazardous industry across the nation. The literature on animal‐related injuries in the agriculture industry is sparse. This analysis aimed to describe cow‐related injuries, the utilization of workers' compensation, and the circumstances of the injuries ...
Komi K. S. Modji, Katherine McCoy, Paul D. Creswell, Morris R. Collin, Carrie Tomasallo, Sheryl Bedno   +5 more
wiley   +1 more source

The lived experience of mothers who give birth after induction of labour in hospital settings in Southern Ethiopia: a phenomenological study. [PDF]

Reprod Health
Abebe A, Setato TN, Bisetegn FS, Dake SK, Nane D.   +4 more
europepmc   +1 more source

Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This case report describes a child with hypomyelinating leukodystrophy type 20 (HLD20), a rare neurodegenerative disorder characterized by impaired myelin formation. The patient presented with multiple neurodevelopmental abnormalities, including delayed motor milestones, seizures, and abnormal facial features.
Malak Alghamdi, Ghaida Alghamdi, Khalid Hundallah, Dima Jamjoom, Naif Almontashiri, Essa Alharbi, Muhammad Umair, Majid Alfadhel   +7 more
wiley   +1 more source

“We are more than diabetes”: a qualitative study of maternity and postnatal care experiences of mothers in England with type 1, type 2 and gestational diabetes

McLeish J, Alderdice F.
europepmc   +1 more source

Challenges in breastfeeding consultation among child health service nurses in Sweden: a qualitative study. [PDF]

Front Pediatr
Ny P, Andersson J, Bergholtz E, Janlöv AC, Ekstrand Ragnar M.   +4 more
europepmc   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong, Caoimhe McKenna, Karen Stals, Antonio Vitobello, Mathilde Renaud, Claudine Rieubland, Michel Guipponi, Christophe Philippe, Paul Vrana, Alisa Gaskell, A. Micheil Innes, Alyssa L. Rippert, Rebecca Ahrens‐Nicklas, Elizabeth Bhoj, Kiersten Keller, Bimal P. Chaudhari, Brandon S. Stone   +16 more
wiley   +1 more source

Mother-child reminiscing of emotional events during the pandemic: The role of changing family relationships and maternal prepandemic depression. [PDF]

Dev Psychol
Feng X, Gong Y, Chan MH, Inboden K, Wang Q.   +4 more
europepmc   +1 more source

Quality of Life of Families Who Have Children With Cornelia de Lange Syndrome in Brazil: Opportunities for Improvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT This exploratory cross‐sectional study aimed to estimate the family quality of life (FQoL) among 70 Brazilian families with children with Cornelia de Lange syndrome (CdLS). Data were collected using sociodemographic and clinical data forms, the Barthel index for activities of daily living, and the Beach Center FQoL Scale, a 5‐point Likert tool
Aline Apis, Beatriz Carvalho Nunes, Thainá Vilella, Rafaela Catelan Martins Pereira, Rui Fernando Pilotto, Lucimar Retto da Silva de Avó, Maria Isabel Melaragno, Carla Maria Ramos Germano, Débora Gusmão Melo   +8 more
wiley   +1 more source

The level of I-FABP and IgA/IgG to beta-lactoglobulin in mothers at risk for gestational diabetes and in their children: association with antibodies to <i>Bifidobacterium adolescentis</i> and <i>Bifidobacterium breve</i>. [PDF]

Front Immunol
Vorobjova T, Tagoma A, Peterson C, Talja I, Bärenson A, Alnek K, Janson H, Metsküla K, Kirss A, Sepp E, Rööp T, Kõljalg S, Uibo R.   +12 more
europepmc   +1 more source

Addressing the Diagnostic Odyssey for Adults With Neurodevelopmental Disabilities: Case Study of an Individual With Mandibulofacial Dysostosis With Microcephaly

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Whole exome sequencing (WES) has been widely used in the pediatric setting to increase diagnostic yield, provide treatment options, and to estimate reoccurrence risks. However, there is limited knowledge regarding the utility of this technology in adults with neurodevelopmental disabilities.
Ruhi Shah, Neora Shifrin, Mary Ellen Keogh, Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon   +6 more
wiley   +1 more source