(Q73497745)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

title

Primary immunodeficiency diseases in Norway (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

A Stray-Pedersen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

T G Abrahamsen

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

S S Frøland

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

publication date

1 November 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

Journal of Clinical Immunology

4 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

4 November 2019

page(s)

477-485

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11202238 AND SRC:MED&resulttype=core&format=json

X-CGDbase: a database of X-CGD-causing mutations

4 November 2019

cites work

1 reference

12 December 2020

Clinical spectrum of X-linked hyper-IgM syndrome

1 reference

12 December 2020

Transient B cell immaturity with intractable diarrhoea: A possible new immunodeficiency syndrome

1 reference

12 December 2020

Primary immunodeficiencies in Switzerland: first report of the national registry in adults and children

1 reference

12 December 2020

Prevalence of a mutation causing C2 deficiency in systemic lupus erythematosus.

1 reference

12 December 2020

Mutation Screening of the BTK Gene in 56 Families With X-Linked Agammaglobulinemia (XLA): 47 Unique Mutations Without Correlation to Clinical Course

1 reference

12 December 2020

Registry of primary immunodeficiencies in Switzerland

1 reference

12 December 2020

CD40Lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome

1 reference

12 December 2020

Primary immunodeficiency syndromes in Italy: a report of the national register in children and adults

1 reference

12 December 2020

Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype

1 reference

12 December 2020

Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: identification of twelve different mutations in the WASP gene

1 reference

12 December 2020

Primary immunodeficiency diseases. Report of a WHO scientific group

1 reference

12 December 2020

Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

1 reference

12 December 2020

Primary immunodeficiency diseases in Latin America: first report from eight countries participating in the LAGID. Latin American Group for Primary Immunodeficiency Diseases

1 reference

12 December 2020

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

1 reference

12 December 2020

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

1 reference

12 December 2020

Chronic mucocutaneous candidiasis. Immunologic studies of three generations of a single family

1 reference

12 December 2020

A multiinstitutional survey of the Wiskott-Aldrich syndrome.

1 reference

12 December 2020

Primary immunodeficiency register, United Kingdom: update 1992.

1 reference

12 December 2020

Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effect

1 reference

12 December 2020

Pathophysiology and treatment of severe chronic neutropenia

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12 December 2020

Familial disseminated infection due to atypical mycobacteria with childhood onset

1 reference

12 December 2020

Primary antibody deficiency in Arabs: first report from eastern Saudi Arabia

1 reference

12 December 2020

Primary immunodeficiency disorders in Sweden: Cases among children, 1974?1979

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12 December 2020

The spectrum of primary immunodeficiency disorders in Australia

1 reference

12 December 2020

Genetic aspects of complement component C8 in Norwegian meningococcal disease patients

1 reference

12 December 2020

Immunodeficiency mutation databases--a new research tool

1 reference

12 December 2020

Primary immunodeficiency syndrome in Japan. I. Overview of a nationwide survey on primary immunodeficiency syndrome

1 reference

12 December 2020

Mutation analysis of IL2RG in human X-linked severe combined immunodeficiency.

1 reference

12 December 2020

Primary immunodeficiency syndrome in Spain: first report of the National Registry in Children and Adults

1 reference

12 December 2020

Hereditary angio-oedema: new clinical observations and autoimmune screening, complement and kallikrein-kinin analyses.

1 reference

12 December 2020

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants

1 reference

12 December 2020

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

1 reference

12 December 2020

Prevalence, genetics and clinical presentation of chronic granulomatous disease in Sweden

1 reference

12 December 2020

Low prevalence of complement deficiencies among patients with meningococcal disease in Norway

1 reference

12 December 2020