Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

about

Delayed Diagnosis and Complications of Predominantly Antibody Deficiencies in a Cohort of Australian Adults.Assessing Disease Severity in Common Variable Immunodeficiency Disorders (CVID) and CVID-Like Disorders

P2860

Q55363912-6F0E4522-721C-498F-B8DC-B652F4FC4C9C Q57490109-421B1E73-CB52-4CB9-B5C1-4141F968825F

P2860

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

Item

http://www.wikidata.org/entity/Q42369096

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@en

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@nl

type

Item

label

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@en

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@nl

prefLabel

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@en

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@nl

P1476

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

@en

P2093

Arja H Aalto

http://www.w3.org/2001/XMLSchema#string

Asko Järvinen

http://www.w3.org/2001/XMLSchema#string

Eero Mattila

http://www.w3.org/2001/XMLSchema#string

Jannica S Selenius

http://www.w3.org/2001/XMLSchema#string

Pekka Suomalainen

http://www.w3.org/2001/XMLSchema#string

Risto Pietikäinen

http://www.w3.org/2001/XMLSchema#string

Sampsa Pikkarainen

http://www.w3.org/2001/XMLSchema#string

Sanna Siitonen

http://www.w3.org/2001/XMLSchema#string

P2860

Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders

Analysis of protein-coding genetic variation in 60,706 humans

Comparison of diagnostic criteria for common variable immunodeficiency disorder

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies)

Terminal deletion of 11q with significant late-onset combined immune deficiency.

Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti-Salmonella typhi Vi IgG Describe a Normal Polysaccharide Response

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

P304

1190

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3389/FIMMU.2017.01190

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Juha Kere

Janna Saarela

Elisabet Einarsdottir

Mikko Seppänen

Martti Färkkilä

Timi Martelius

P577

2017-09-28T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29033928

http://www.w3.org/2001/XMLSchema#string

P921

Finland

P932

5625003

http://www.w3.org/2001/XMLSchema#string

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

about

P2860

P2860

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P932