(Q36451114)

14 August 2017

Familial combined cellular and humoral immune defect with multisystem granulomata (English)

1 reference

14 August 2017

W. H. Perks

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A644530

17 July 2022

I. S. Petheram

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A644530

17 July 2022

language of work or name

English

0 references

publication date

1 February 1978

1 reference

PMC publication ID

470855

full work available at URL

14 August 2017

https://europepmc.org/articles/PMC470855

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A644530

https://europepmc.org/articles/PMC470855?pdf=render

17 July 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A644530

https://syndication.highwire.org/content/doi/10.1136/thx.33.1.101

17 July 2022

1 reference

https://api.crossref.org/works/10.1136/THX.33.1.101

1 September 2023

1 reference

14 August 2017

33

1 reference

14 August 2017

1

1 reference

14 August 2017

101-105

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

14 August 2017

1 reference

Familial hypogammaglobulinemia, splenomegaly and leukopenia. With a review of the etiological factors of the hypogammaglobulinemias

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

B and T lymphocytes in primary immunodeficiency disease in man.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Elevation of Serum Angiotensin-Converting Enzyme in Gaucher's Disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Elevation of serum angiotension-converting-enzyme (ACE) level in sarcoidosis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Lymphocyte purine 5'-nucleotidase edficiency in primary hypogammaglobulinaemia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Clinical, serologic and leukocyte function studies on patients with idiopathic “acquired” agammaglobulinemia and their families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Identification and function of T cells in the peripheral blood of patients with hypogammaglobulinaemia.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=470855

PRIMARY "ACQUIRED" HYPOGAMMAGLOBULINEMIA; CLINICAL AND GENETIC ASPECTS OF NINE CASES

28 June 2018

1 reference

12 December 2020

Inherited "acquired" hypogammaglobulinaemia

1 reference

12 December 2020

Syndrome of hypogammaglobulinemia, splenomegaly and hypersplenism

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

Hypogammaglobulinemia, depression of delayed-type hypersensitivity, and granuloma formation

1 reference

12 December 2020

Identifiers

DOI

10.1136/THX.33.1.101

1 reference

14 August 2017

1 reference

PMC publication ID

470855

14 August 2017

1 reference

PMC publication ID

470855