Results 211 to 220 of about 1,669,600 (380)
Factor Price Equalization in Finland [PDF]
The Heckscher-Ohlin trade model leads to clear conclusions on the absolute and relative factor prices in a two-commodity specification of the model where both commodities are produced and factors can move freely within the economy.
Aki Kangasharju +2 more
core
Capacitive, charge‐domain compute‐in‐memory (CIM) stores weights as capacitance,eliminating DC sneak paths and IR‐drop, yielding near‐zero standbypower. In this perspective, we present a device to systems level performance analysis of most promising architectures and predict apathway for upscaling capacitive CIM for sustainable edge computing ...
Kapil Bhardwaj +2 more
wiley +1 more source
What We Don't Speak of: Exploring the Impact of Historical Trauma and Discrimination on the Health and Well-Being of Sweden Finns. [PDF]
Strand M, Lindqvist M.
europepmc +1 more source
Gambling, violent behaviour and attitudes towards violence among adolescent gamblers in Finland
Tiina Räsänen +4 more
openalex +1 more source
This condensed version of chao-dyn/9509010 will be the main hand-out for a course on algorithmic information theory to be given 22-29 May 1996 at the Rovaniemi Institute of Technology, Rovaniemi, Finland (see announcement at http://www.rotol.fi ...
Chaitin Ibm Box, G. J. Chaitin
core +4 more sources
A Systematic Review and Meta‐Analysis of the Birth Prevalence of Turner Syndrome
ABSTRACT Turner syndrome, a chromosomal disorder, causes short stature, pubertal arrest, amenorrhea, and infertility in females. Prevalence estimates vary widely; however, reliable estimates are important for public health initiatives. Therefore, a meta‐analysis was undertaken.
David Hinds +5 more
wiley +1 more source
Aging in place or relocating? Older adults' housing decisions in Taiwan and Finland. [PDF]
Chou YC, Jolanki O, Chen BW.
europepmc +1 more source
Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää +14 more
wiley +1 more source
Associations of Domain-Specific Physical Activity With Mental Health Symptoms Among Finnish Employed Adults: A Population-Based Study. [PDF]
Jussila JJ +8 more
europepmc +1 more source

