Educational paper: Defects in number and function of neutrophilic granulocytes causing primary immunodeficiency (Q37942048)

25 August 2017

2 references

31 December 2023

Educational paper: Defects in number and function of neutrophilic granulocytes causing primary immunodeficiency (English)

1 reference

primary immunodeficiency disease

25 August 2017

1 reference

1 reference

2

Taco W Kuijpers

1 reference

PMCID

3197933

25 August 2017

J Merlijn van den Berg

series ordinal

1

object named as

J Merlijn van den Berg

1 reference

25 August 2017

4 October 2011

1 reference

PMCID

3197933

European Journal of Pediatrics

25 August 2017

1 November 2011

1 reference

31 December 2023

2 references

25 August 2017

31 December 2023

170

1 reference

25 August 2017

11

1 reference

25 August 2017

1369-1376

1 reference

Creative Commons Attribution-NonCommercial 4.0 International

25 August 2017

1 reference

https://scigraph.springernature.com/pub.10.1007/s00431-011-1584-5

31 December 2023

exact match

0 references

cites work

Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Genetic defects in severe congenital neutropenia: emerging insights into life and death of human neutrophil granulocytes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Educational paper: Primary immunodeficiencies in children: a diagnostic challenge

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Cyclic and chronic neutropenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Neutrophil granules in health and disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Primary immunodeficiencies of protective immunity to primary infections

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

6 September 2017

Eponym. Kostmann disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Leukocyte adhesion deficiency type II: long-term follow-up and review of the literature

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Genetic etiologies of leukocyte adhesion defects

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Chronic granulomatous disease: the European experience

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

A syndrome with congenital neutropenia and mutations in G6PC3

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

6 September 2017

Chediak-Higashi syndrome

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

6 September 2017

https://api.crossref.org/works/10.1007%2FS00431-011-1584-5

Granulocyte transfusions in neutropaenic children: a systematic review of the literature.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Getting to the site of inflammation: the leukocyte adhesion cascade updated

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Growth factor independence-1 (Gfi-1) plays a role in mediating specific granule deficiency (SGD) in a patient lacking a gene-inactivating mutation in the C/EBPepsilon gene

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Diagnosis and clinical course of autoimmune neutropenia in infancy: analysis of 240 cases.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Toll-like receptor responses in IRAK-4-deficient neutrophils

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Kostmann disease with developmental delay in three patients.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

LAD-1/variant syndrome is caused by mutations in FERMT3.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Toll-like receptors stimulate human neutrophil function

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3197933

Hematopoietic stem cell transplantation in severe congenital neutropenia

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-011-1584-5

Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21968907

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00431-011-1584-5

1 reference

25 August 2017

1 reference

25 August 2017

1 reference

PMCID

3197933