Familial combined cellular and humoral immune defect with multisystem granulomata

about

Development of granulomatous common variable immunodeficiency subsequent to infection with Toxoplasma gondii.Acquired common variable hypogammaglobulinaemia and lymphoedema.

P2860

Q35867518-8D4D6CD9-D37B-4F1E-8E00-314358AB998C Q36722147-71A1B524-1D24-4C14-82CB-3E298F25D86B

P2860

Familial combined cellular and humoral immune defect with multisystem granulomata

Item

http://www.wikidata.org/entity/Q36451114

description

1978 nî lūn-bûn

@nan

1978年の論文

@ja

1978年学术文章

@wuu

1978年学术文章

@zh-cn

1978年学术文章

@zh-hans

1978年学术文章

@zh-my

1978年学术文章

@zh-sg

1978年學術文章

@yue

1978年學術文章

@zh

1978年學術文章

@zh-hant

name

Familial combined cellular and humoral immune defect with multisystem granulomata

@ast

Familial combined cellular and humoral immune defect with multisystem granulomata

@en

type

Item

label

Familial combined cellular and humoral immune defect with multisystem granulomata

@ast

Familial combined cellular and humoral immune defect with multisystem granulomata

@en

prefLabel

Familial combined cellular and humoral immune defect with multisystem granulomata

@ast

Familial combined cellular and humoral immune defect with multisystem granulomata

@en

P1476

Familial combined cellular and humoral immune defect with multisystem granulomata

@en

P2093

Perks WH

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

Petheram IS

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

P2860

Agammaglobulinemia

B and T lymphocytes in primary immunodeficiency disease in man.

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

Lymphocyte purine 5'-nucleotidase edficiency in primary hypogammaglobulinaemia.

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

Elevation of serum angiotensin-converting enzyme in Gaucher's disease.

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

Clinical, serologic and leukocyte function studies on patients with idiopathic "acquired" agammaglobulinemia and their families.

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

P304

101-105

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

P31

scholarly article

P356

10.1136/THX.33.1.101

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

P407

English

P433

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

P478

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

P577

1978-02-01T00:00:00Z

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

P5875

22496837

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P698

644530

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

P932

470855

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

Familial combined cellular and humoral immune defect with multisystem granulomata

about

P2860

P2860

Familial combined cellular and humoral immune defect with multisystem granulomata

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P5875

P698

P932