Clinical phenotype of schizophrenia in a Finnish isolate.

Clinical phenotype of schizophrenia in a Finnish isolate.

Item
http://www.wikidata.org/entity/Q43934761
An evaluation of variation in published estimates of schizophrenia prevalence from 1990─2013: a systematic literature reviewReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesPsychosis among "healthy" siblings of schizophrenia patients.Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.Kraepelin's dichotomy is true: contrasting brain dysfunction at the extremes of human growth and maturation. Excitability, the fundamental property of nervous tissue, is affected.Growth pattern and risk of schizophrenia.Both low birthweight and high birthweight are associated with cognitive impairment in persons with schizophrenia and their first-degree relatives.
P2860

Clinical phenotype of schizophrenia in a Finnish isolate.

Item
http://www.wikidata.org/entity/Q43934761
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
@zh-hant
name
Clinical phenotype of schizophrenia in a Finnish isolate.
@en
Clinical phenotype of schizophrenia in a Finnish isolate.
@nl
type
label
Clinical phenotype of schizophrenia in a Finnish isolate.
@en
Clinical phenotype of schizophrenia in a Finnish isolate.
@nl
prefLabel
Clinical phenotype of schizophrenia in a Finnish isolate.
@en
Clinical phenotype of schizophrenia in a Finnish isolate.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
Clinical phenotype of schizophrenia in a Finnish isolate
@en
P2093
P304
P31
P356
10.1016/S0920-9964(03)00007-0
P407
P433
P478
P50
P577
P698
P921