(Q44624038)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

title

Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

severe congenital neutropenia

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Asghar Aghamohammadi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Qiang Pan-Hammarström

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

5

Lennart Hammarstrom

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Asghar Ramyar

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

1 reference

2 July 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

International Archives of Allergy and Immunology

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

147

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

255-259

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee

9 January 2020

cites work

1 reference

The hyper IgM syndrome--an evolving story

21 January 2018

1 reference

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

21 January 2018

1 reference

The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.

21 January 2018

1 reference

Clinical spectrum of X-linked hyper-IgM syndrome

21 January 2018

1 reference

CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000142050

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18594157%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference