Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Publication year range
1.
J Pers Soc Psychol ; 79(1): 66-76, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10909878

ABSTRACT

In 5 studies, the authors examined people's perceptions of the endowment effect, or the tendency to value an object more once one owns it. In the 1st 2 studies, the authors documented egocentric empathy gaps between owners and buyers regarding the endowment effect: Both owners and buyers overestimated the similarity between their own valuation of a commodity and the valuation of people in the other role. The next 2 studies showed that these empathy gaps may lead to reduced earnings in a market setting. The final study showed that egocentric empathy gaps stem partly from people's misprediction of what their own valuation would be if they were in the other role.


Subject(s)
Attitude , Choice Behavior , Empathy , Self Concept , Social Perception , Adult , Female , Humans , Male , United States
2.
Ned Tijdschr Geneeskd ; 144(50): 2412-5, 2000 Dec 09.
Article in Dutch | MEDLINE | ID: mdl-11145098

ABSTRACT

In 1988 three families were described in this journal with Fabry's disease, an X-linked recessive lysosomal storage disorder caused by the deficiency of alpha-galactosidase A. A fourth family contained four affected men of whom one was unavailable for evaluation. The other three had the same mutation in de alpha-galactosidase gene, notably Gln386Stop, leading to the change of a glutamine codon into a stop codon. Genetic investigation in one of the other families revealed the Met72Arg mutation. The classical symptoms of the disease (angiokeratomata, acroparaesthesias, hypohidrosis and lucid areas in the cornea) are frequently only recognized after a doctor's delay that may be as long as decades. The recognition of this disease is even more important now, as therapeutic possibilities are in sight.


Subject(s)
Amino Acid Metabolism, Inborn Errors/diagnosis , Fabry Disease/diagnosis , Fabry Disease/genetics , Mutation , alpha-Galactosidase/genetics , Adult , Amino Acid Metabolism, Inborn Errors/complications , Amino Acid Metabolism, Inborn Errors/genetics , Amino Acid Metabolism, Inborn Errors/physiopathology , Diagnosis, Differential , Fabry Disease/complications , Fabry Disease/physiopathology , Female , Genetic Predisposition to Disease , Genetic Testing , Humans , Male , Middle Aged , Pedigree , Phenotype , Sex Factors , alpha-Galactosidase/blood
SELECTION OF CITATIONS
SEARCH DETAIL
...