(Q35674223)

9 August 2017

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title

Pulmonary complications of primary immunodeficiencies (English)

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9 August 2017

Rebecca H Buckley

1

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9 August 2017

publication date

1 January 2004

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Paediatric Respiratory Reviews

9 August 2017

published in

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9 August 2017

volume

5 Suppl A

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9 August 2017

page(s)

S225-33

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Primary immunodeficiency diseases due to defects in lymphocytes

9 August 2017

cites work

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7 January 2021

X-linked agammaglobulinemia

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7 January 2021

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

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7 January 2021

Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

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7 January 2021

Bronchiectasis in hypogammaglobulinaemia--a computed tomography assessment

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7 January 2021

Common variable immunodeficiency: clinical and immunological features of 248 patients.

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7 January 2021

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

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7 January 2021

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

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7 January 2021

NIH conference. New insights into common variable immunodeficiency

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7 January 2021

Enhanced T cell apoptosis in common variable immunodeficiency: negative role of the fas/fasligand system and of the Bcl-2 family proteins and possible role of TNF-RS

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7 January 2021

Chronic enteroviral meningoencephalitis in agammaglobulinemic patients

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7 January 2021

Granulomatous disease in common variable immunodeficiency

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7 January 2021

Incidence of cancer in 98 patients with common varied immunodeficiency

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7 January 2021

Transplantation of thymus tissue in complete DiGeorge syndrome

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7 January 2021

Advances in the understanding and treatment of human severe combined immunodeficiency

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7 January 2021

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

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7 January 2021

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

1 reference

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7 January 2021

Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans

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7 January 2021

Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency.

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7 January 2021

Cutting edge: the common gamma-chain is an indispensable subunit of the IL-21 receptor complex

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7 January 2021

Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid development.

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7 January 2021

Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency

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7 January 2021

RAG mutations in human B cell-negative SCID.

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7 January 2021

Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease

1 reference

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7 January 2021

A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p

1 reference

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7 January 2021

Chondroosseous dysplasia in severe combined immunodeficiency due to adenosine deaminase deficiency (chondroosseous dysplasia in ADA deficiency scid)

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

1 reference

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7 January 2021

Correction of purine nucleoside phosphorylase deficiency by transplantation of allogeneic bone marrow from a sibling

1 reference

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7 January 2021

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

1 reference

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7 January 2021

The interaction between Cdc42 and WASP is required for SDF-1-induced T-lymphocyte chemotaxis.

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

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7 January 2021

DNA-dependent protein kinase catalytic subunit: a relative of phosphatidylinositol 3-kinase and the ataxia telangiectasia gene product

1 reference

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7 January 2021

Dual roles of ATM in the cellular response to radiation and in cell growth control.

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Ataxia telangiectasia: cell signaling, cell death and the cell cycle

1 reference

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7 January 2021

The hyper-IgE syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Hyperimmunoglobulinemia E Syndrome: Radiographic Observations

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7 January 2021

Hyperimmunoglobulinemia E syndrome: association with osteoporosis and recurrent fractures.

1 reference

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7 January 2021

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

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7 January 2021

Immunodeficiency diseases caused by defects in phagocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Adhesion molecule deficiencies and their clinical significance

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Human leukocyte adhesion deficiency: molecular basis for a defective immune response to infections of the skin

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Infectious diseases associated with complement deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1526-0542%2804%2990043-7

7 January 2021

10.1016/S1526-0542(04)90043-7

Identifiers

DOI

1 reference

9 August 2017

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