Results 231 to 240 of about 1,475,270 (301)

A systematic review of educational interventions to enhance ethical sensitivity in nursing students in Asia and the Middle East. [PDF]

BMC Med Ethics
Shi X, Wang R, Li Y, Zeng L.
europepmc   +1 more source

Variants in AKR1D1 and Infant Mortality: Should Bile Acid Screening be a Routine Part of Newborn Screening?

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic pathogenic variants in AKR1D1 cause Δ4‐3‐oxosteroid 5β‐reductase deficiency, disrupt bile acid synthesis, and result in Congenital Bile Acid Synthesis defect type 2 (CBAS2). CBAS2 presents in infancy with cholestasis, coagulopathy, and failure to thrive.
Jade Hudson, Stephanie Hyunh, Bojana Rakic, Cornelius Boerkoel   +3 more
wiley   +1 more source

Ethics and dilemmas regarding acceptance of COVID-19 vaccine among people living in an Indian metropolitan city during the pandemic: a qualitative study. [PDF]

BMJ Open
Raj JP, Balasubramanian S, Nellikal S, Sawant DA, Sadawarte D.   +4 more
europepmc   +1 more source

Denial of Inpatient Genetic Testing: A Study on Outpatient Yield and Outcomes

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic conditions suspected in children often require genetic testing for accurate diagnoses, but testing remains costly. Case management teams review genetic test requests to improve access for patients while reducing the financial burden for medical institutions.
Cindy Y. Canales, Kathleen Shields, Meagan Choates, Paul Hillman, Laura Farach, Theresa Wittman, Kathryn Leal   +6 more
wiley   +1 more source

Shaping professional identity in dentistry: a cross-sectional study of value prioritization among undergraduate students. [PDF]

BMC Med Educ
Nafea ET, Alhussin AM, Alkuhayli SA, Aljohani MO.   +3 more
europepmc   +1 more source

Expanding the Genotype–Phenotype Correlation of Marden–Walker Syndrome due to PIEZO2 Gene Variants: A Case Report From Brazil

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston, Carolina de Souza Araujo, Fernanda Araujo Romera, André Luis Ferreira, Érica Trovisco Martins, Carolina Galhós de Aguiar, José Eduardo Mourão Santos, Rodrigo Ragazzini, Daniela Testoni Costa‐Nobre, Ana Claudia Yoshikumi Prestes, Allan Chiaratti de Oliveira, Eduardo Perrone, Débora Gusmão Melo, Anne Caroline Barbosa Teixeira, Antonio Victor Campos Coelho, Caio Robledo D’Angioli Costa Quaio, Carolina Araujo Moreno, Eduardo Perrone, Jose Bandeira do Nascimento Junior, Jessica Grasiela Araujo Espolaor, Joana Rosa Marques Prota, Joao Bosco de Oliveira Filho, Jose Ricardo Magliocco Ceroni, Kelin Chen, Letícia Torres Ferreira, Lucas Santos de Santana, Luciana Souto Mofatto, Luiza do Amaral Virmond, Marina de Franca Basto Silva, Michele Patricia Migliavacca, Renata Moldenhauer Minillo, Renata Yoshiko Yamada, Roberta Sitnik, Tatiana Ferreira de Almeida, Thiago Yoshinaga Tonholo Silva, Vivian Pedigone Cintra   +35 more
wiley   +1 more source

Interprofessional Competencies for Effective Interprofessional Collaborative Practices Amongst Intensive Care Unit Teams in the North West Province, South Africa: A Cross-Sectional Survey. [PDF]

Health Serv Insights
Zenani NE, Scholtz S, Heymans Y, Christmals C.   +3 more
europepmc   +1 more source

Exploring allied health research capacity in Nigeria: a qualitative study of enablers and barriers. [PDF]

BMC Health Serv Res
Osaigbovo II, Ogboghodo EO, Obaseki CO, Nwaogwugwu JC.   +3 more
europepmc   +1 more source

Development and validation of a competency-based assessment tool for public health workers in Shanghai community health centers: a population-based study. [PDF]

Hum Resour Health
Chang R, Zhang M, Li R, Zhu Q, Dong Y, Liu Y, Chen Y, Wang Z, Huang H, Cai Y.   +9 more
europepmc   +1 more source