Perceived emotional support mediates the association between childhood family adversity and adolescent mental health in the UK millennium cohort. [PDF]
Adjei NK +8 more
europepmc +1 more source
Determinants of Poverty during Transition: Household Survey Evidence from Ukraine [PDF]
The paper analyzes the incidence, the severity and the determinants of household poverty in Ukraine during transition using two comparable surveys from 1996 and 2004.
Brück, Tilman +3 more
core
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
wiley +1 more source
Emergent poverty traps at multiple levels impede social mobility. [PDF]
Dupont C, Roy D.
europepmc +1 more source
Measurement of Chronic and Transient Poverty: Theory and Application to Pakistan [PDF]
This paper investigates how to characterize each person's poverty status when his/her welfare level fluctuates and how to aggregate the status into chronic and transient poverty measures.
Kurosaki, Takashi
core
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco +18 more
wiley +1 more source
Corruption, poverty and inflation as enablers of AMR in low- and middle-income countries: finding the link and addressing the gaps. [PDF]
Egwu KC +5 more
europepmc +1 more source
ANALYSIS OF POVERTY IN JAVA-BALI ISLAND AND REGIONS OUTSIDE JAVA-BALI
Sri Nathasya +2 more
openalex +2 more sources
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
wiley +1 more source

