Results 261 to 270 of about 523,743 (349)

Stress, Health, and Injury Among Illinois Farmers

American Journal of Industrial Medicine, EarlyView.
ABSTRACT Objectives The goal of this cross‐sectional study was to characterize stress, injury, and chronic health conditions among agricultural producers in Illinois. The objectives were to: (1) describe the prevalence and nature of work‐related injuries; (2) describe chronic health conditions, stress, and symptoms of mental health conditions; and (3 ...
Josie M. Rudolphi, Salah Issa, Courtney Cuthbertson, Kaleigh Barnett   +3 more
wiley   +1 more source

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

Gender distribution of Top Doctors in otolaryngology-head and neck surgery. [PDF]

PLoS One
DiNardo LA, Reese AD, Raghavan M, Sullivan M, Carr MM.   +4 more
europepmc   +1 more source

Application of Nd: YAG and KTP Contact Lasers in Surgery for Head and Neck Tumors

, 2003
Masaru Sugiyama, Tamiko Dohmen
openalex   +2 more sources

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

Application of organoids in otolaryngology: head and neck surgery. [PDF]

Eur Arch Otorhinolaryngol
Zhu H, Qu S, Deng Y, Gong M, Xiang Y, Teng Y, Ye D.   +6 more
europepmc   +1 more source

ENDOSCOPIC NECK SURGERY USING THE CERVICAL REGION-LIFTING METHOD THE UNDERSTANDING AND TRAINING OF THE ENDOSCOPIC SURGERY; A GUIDE FOR HEAD AND NECK SURGEONS

, 2003
Hideyuki Kataoka, Hiroya Kitano, Takashi Kinoshita, Msamitsu HIRANO   +3 more
openalex   +2 more sources

Patient With Prolidase Deficiency due to an Homozygous PEPD Variant, Induced by Paternal Uniparental Isodisomy of Chromosome 19

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Uniparental disomy (UPD) is a rare phenomenon in which both copies of a chromosome are inherited from a single parent. This can lead to genomic imprinting disorders and recessive disorders due to the presence of recessive pathogenic variants in both alleles. Additionally, depending on the mechanisms by which UPD occurs, mosaic aneuploidies may
Marta Carreño‐Hidalgo, Raquel Muñoz‐Siles, Vanesa López‐González, Lidia Carreño‐Gago, Lluís Armengol Dulcet   +4 more
wiley   +1 more source

Assessment of decision-making with locally run and web-based large language models versus human board recommendations in otorhinolaryngology, head and neck surgery. [PDF]

Eur Arch Otorhinolaryngol
Buhr CR, Ernst BP, Blaikie A, Smith H, Kelsey T, Matthias C, Fleischmann M, Jungmann F, Alt J, Brandts C, Kämmerer PW, Foersch S, Kuhn S, Eckrich J.   +13 more
europepmc   +1 more source

Survivorship of Individuals With Double Heterozygosity for Achondroplasia and Type 2 Collagenopathy

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Historically, double heterozygosity, or a diagnosis of two separate, dominant genetic conditions, was often thought to be lethal in individuals with autosomal dominant skeletal dysplasias. In previously published studies of individuals with dual dysplasia diagnoses of achondroplasia and type 2 collagenopathy, infants died of respiratory ...
Valerie R. Schwartz, Andrea Schelhaas, Angela L. Duker, Ricki S. Carroll   +3 more
wiley   +1 more source