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Literature DB >> 14219207

IMMUNOLOGIC DEFICIENCY IN ATAXIA TELANGIECTASIA.

A H EISEN, G KARPATI, T LASZLO, F ANDERMANN, J P ROBB, H L BACAL.

Abstract

Entities: Disease

Keywords: ADOLESCENCE; AGAMMAGLOBULINEMIA; ALPHA GLOBULIN; ANTIGEN-ANTIBODY REACTIONS; ATAXIA; BETA GLOBULIN; BLOOD PROTEIN ELECTROPHORESIS; CHILD; HEMAGGLUTINATION; LEUKOPENIA; LYMPHOCYTES; NEUTRALIZATION TESTS; SKIN TESTS; SKIN TRANSPLANTATION; TELANGIECTASIS; THYMUS GLAND; TRANSPLANTATION IMMUNOLOGY; TRANSPLANTATION, HOMOLOGOUS

Mesh：

Substances：

Year: 1965 PMID： 14219207 DOI： 10.1056/NEJM196501072720104

Source DB: PubMed Journal: N Engl J Med ISSN： 0028-4793 Impact factor: 91.245

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Cited

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11 in total

1. A novel mouse model for ataxia-telangiectasia with a N-terminal mutation displays a behavioral defect and a low incidence of lymphoma but no increased oxidative burden.

Authors: Andrew Campbell; Brittany Krupp; Jared Bushman; Mark Noble; Christoph Pröschel; Margot Mayer-Pröschel
Journal: Hum Mol Genet Date: 2015-08-26 Impact factor: 6.150

2. Dysgammaglobulinaemia type IV C.

Authors: J R Hobbs; A Russell; S M Worlledge
Journal: Clin Exp Immunol Date: 1967-09 Impact factor: 4.330

3. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).

Authors: C E Parker; J Mavalwala; R Koch; A Hatashita; A Derencsenyi
Journal: Calif Med Date: 1972-10

4. Mutation of ataxia-telangiectasia mutated is associated with dysfunctional glutathione homeostasis in cerebellar astroglia.

Authors: Andrew Campbell; Jared Bushman; Joshua Munger; Mark Noble; Christoph Pröschel; Margot Mayer-Pröschel
Journal: Glia Date: 2015-10-15 Impact factor: 7.452

IMMUNOLOGIC DEFICIENCY IN ATAXIA TELANGIECTASIA.

1. A novel mouse model for ataxia-telangiectasia with a N-terminal mutation displays a behavioral defect and a low incidence of lymphoma but no increased oxidative burden.

2. Dysgammaglobulinaemia type IV C.

3. The syndrome associated with the partial deletion of the long arms of chromosome 18 (18q-).

4. Mutation of ataxia-telangiectasia mutated is associated with dysfunctional glutathione homeostasis in cerebellar astroglia.

5. Diagnostic considerations in ataxia-telangiectasia.

6. Immunological investigations in two brothers with ataxia telangiectasia Louis-Bar.

7. The association of autoimmune diseases and anti-IgA antibodies in patients with selective IgA deficiency.

8. Antibody responses in vivo in chromosome instability syndromes with immunodeficiency.

9. [Ataxia-telangiectasia (Louis-Bar-syndrome). Report on seven cases].

10. Antibody response to a seven-valent pneumococcal conjugated vaccine in patients with ataxia-telangiectasia.