Results 161 to 170 of about 146,457 (308)

Health Biotechnology to 2030:OECD International Futures Project on “The Bioeconomy to 2030: Designing a Policy Agenda” [PDF]

, 2007
Bruce, Ann, Chataway, Joanna, Tait, Joyce, Wield, David   +3 more
core  

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Strengthening funding and integration for NTD elimination: insights from the 2025 Annual Meeting of National NTD Programme Managers in the WHO African Region. [PDF]

BMC Proc
Juma E, Achu D, Barry A, Beshah A, Adjami AAG, Kello AB, Ebeja AK, Jatta B, Bakajika D, Nduba DY, Sen D, Lekhanya-Mohatla FM, Zoure HGM, Cano J, Davi KM, Sanfo MS, Kaonga N, Mwinzi P, Ndayiziga SM, Barogui YTM, Makino Y, Farham B, Impouma B.   +22 more
europepmc   +1 more source

Animal advocacy in a pluralist society [PDF]

Human concern with the moral status of non-human animals can be seen to stretch quite some\ud way back into human history. In ancient Greece such concerns were considered to be very\ud much a part of the ethical agenda, with thinkers on the issue being divided into four main\ud schools of thought: animism; vitalism; mechanism; and anthropocentrism ...
openaire  

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

Youth as change makers on antimicrobial resistance: an evidence-based call-to-action. [PDF]

Nat Commun
Mitchell J, Khan SF, Almazidou C, Barón-Cruz A, Bazzi RA, Estrella-Porter P, Gicheru NK, Khatic K, Mosha MJ, Ungurenci M, Noali BEP, Wong K, Zanni F.   +12 more
europepmc   +1 more source

Homelessness Service Usage Patterns of 30,000 Homeless and At‐Risk Households: The Melbourne Access Point Study

Australian Journal of Social Issues, EarlyView.
ABSTRACT Over the last three decades, overseas researchers have utilised administrative data to identify distinct patterns in shelter use. In Australia, the use of administrative data to understand service utilisation patterns among people ‘at risk’ of homelessness and experiencing homelessness is limited.
Godwin Kavaarpuo, Kathryn Daley, Guy Johnson   +2 more
wiley   +1 more source

Toward One Health Institutionalization: harnessing stakeholder network as leverage to strengthen health security in Libya. [PDF]

Front Public Health
Saidouni A, Ghazy RM, Zorgani A, Elahmer O, Natuh D, Osman RM, El Halafi A, Zouiten A.   +7 more
europepmc   +1 more source

Trauma‐Informed Practice in Welfare‐to‐Work and Employment Services: A Scoping Review

Australian Journal of Social Issues, EarlyView.
ABSTRACT There is increasing recognition within welfare services, including employment services, that many participants may have histories of trauma. Research suggests that experiences of trauma not only impact individuals' psychosocial health but also vocational elements such as job performance, employability, career progression, and financial ...
Emily Corbett, Michael McGann, Mark Considine, René Rejón   +3 more
wiley   +1 more source

Navigating identity and professional life: A qualitative study of LGBTQ+ genetic counselors' workplace experiences. [PDF]

J Genet Couns
Nelson KL, Zayhowski K, MacFarlane IM.
europepmc   +1 more source