Trends in Burden of Female Infertility During 1990-2021: An Analysis of Data from the Global Burden of Disease Study 2021. [PDF]
Zheng J, Chen X, Yuan A, Ying L.
europepmc +1 more source
INTERNATIONAL RELATIONS OF JAPAN WITH THE COUNTRIES OF CENTRAL ASIA
openaire +1 more source
State-Directed Diffusion of Technology: The Mechanization of Cotton-Farming in Soviet Central Asia [PDF]
When Soviet central planners began to mechanize the cotton harvest in earnest in 1958, they expected more rapid diffusion than the market-driven process that had begun in the United States a decade earlier.
Richard Pomfret
core
Genetic Variation in ADHD‐Related Risk Genes in an Indigenous Population of the Amazon
ABSTRACT Attention‐Deficit/Hyperactivity Disorder (ADHD) is a highly heritable neurodevelopmental disorder; however, its genetic architecture remains poorly explored in Indigenous populations. This study aimed to analyze and characterize genetic variation in 11 genes (ADGRL3, CDH8, DCC, DUSP6, FOXP1, FOXP2, MEF2C, PCDH7, SEMA6D, SORCS3, and ST3GAL3 ...
Hirlesson Paixão de Matos +11 more
wiley +1 more source
Global, regional, and 204 countries burden of disease attributed to secondhand smoke-related COPD, 1990-2021: A secondary data analysis of the Global Burden of Disease Study 2021. [PDF]
Huang Q +7 more
europepmc +1 more source
Theme: Strengthening Regional Cooperation In Central Asia: A Contribution to Long-Term Stability and Sustainable Development of ...
United Nations Special Programme for the Economies of Central Asia (SPECA) +1 more
core
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 +6 more
wiley +1 more source
The shifting burden of tracheal, bronchus and lung cancer in ageing Asia: structural drivers and projections to 2050. [PDF]
Zhu L +5 more
europepmc +1 more source
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with over 400 genetic and many non‐genetic causes implicated in its prenatal development.
Shahrzad Nematollahi +20 more
wiley +1 more source
Burden of chronic kidney disease and its attributable risk factors in 204 countries and territories, 1990-2021: Results from the Global Burden of Disease study 2021. [PDF]
Tao W, Chen C, Zhang J, Jiang X, Deng L.
europepmc +1 more source

