Precautionary Recommendation System in Risk Management: A FMEA-Based Approach. [PDF]
Narlı M.
europepmc +1 more source
Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz +3 more
wiley +1 more source
Preface: ICFM9 – River Basin Disaster Resilience and Sustainability by All [PDF]
T. Koike +10 more
doaj +1 more source
Implementing a suicide risk management protocol as part of a multisite clinical trial: Findings and lessons learned. [PDF]
Chase E +10 more
europepmc +1 more source
Enterprise Asset Management Risks and Management and Control Strategies [PDF]
openalex +1 more source
Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky +8 more
wiley +1 more source
Advancing risk management in nuclear medicine diagnostic and therapy through incident-driven risk management tools. [PDF]
Strigari L +10 more
europepmc +1 more source
LAI Paper Series: “Lean Product Development for Practitioners”: Risk Management in Lean PD
Josef Oehmen, Eric Rebentisch
openalex +1 more source
Enhancing Data Integrity and Legal Accountability: A Blockchain-Driven Approach to Corporate Fraud Risk Management [PDF]
Victor Chinedu Achebe +2 more
openalex +1 more source
Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian +9 more
wiley +1 more source

