Results 121 to 130 of about 811,983 (344)
ABSTRACT Background Classified as carcinogenic to humans by the International Agency for Research on Cancer, aluminum production has been transitioning towards lower polycyclic aromatic hydrocarbon‐emitting prebake smelters. This study explored the risk of cancer and mortality over 20 years follow‐up among a cohort of aluminum prebake smelter workers ...
Natasha Kinsman +7 more
wiley +1 more source
Occupational medicine training in Korea
Won-Jun Choi
doaj +1 more source
AN IMPROVEMENT OF THE RISK MANAGEMENT SYSTEM FOR THE PREVENTION OF OCCUPATIONAL DISEASES
This entry deals with the problem of improvement of the risk management system for prevention of occupational diseases.
V. A. Kaptsov, V. B. Pankova
doaj
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates +6 more
wiley +1 more source
Medical data exchange between family physicians and specialists of occupational medicine
Occupational medicine specialists often demand an access to original medical records kept by patients’ family physicians. Referring medical documentation is often not in accordance with the legislation, though the latter is neither precise nor ...
Grega Strban +2 more
doaj
The Reciprocal Relationship Between Art and Occupational Therapy Practice
Susan Burwash, Ph.D., OTR/L, an occupational therapy professor and artist based in Washington State, provided the cover art for the Winter 2017 issue of the Open Journal of Occupational Therapy (OJOT).
Jennifer Fortuna
doaj +1 more source
Jefferson Award for Excellence in Interprofessional Education [PDF]
In recognition for outstanding contributions to interprofessional education two faculty awards were given by JCIPE to Christine Jerpbak, MD, Department of Family and Community Medicine on May 23, 2010 and E.
core +1 more source
Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat +4 more
wiley +1 more source

