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Literature DB >> 16429382

Phenotypic overlap between infantile systemic lupus erythematosus and Aicardi-Goutières syndrome.

C De Laet, P Goyens, C Christophe, A Ferster, F Mascart, B Dan.

Abstract

Entities: Disease

Mesh：

Year: 2005 PMID： 16429382 DOI： 10.1055/s-2005-873058

Source DB: PubMed Journal: Neuropediatrics ISSN： 0174-304X Impact factor: 1.947

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27 in total

1. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort.

Authors: B Namjou; P H Kothari; J A Kelly; S B Glenn; J O Ojwang; A Adler; M E Alarcón-Riquelme; C J Gallant; S A Boackle; L A Criswell; R P Kimberly; E Brown; J Edberg; A M Stevens; C O Jacob; B P Tsao; G S Gilkeson; D L Kamen; J T Merrill; M Petri; R R Goldman; L M Vila; J-M Anaya; T B Niewold; J Martin; B A Pons-Estel; J M Sabio; J L Callejas; T J Vyse; S-C Bae; F W Perrino; B I Freedman; R H Scofield; K L Moser; P M Gaffney; J A James; C D Langefeld; K M Kaufman; J B Harley; J P Atkinson
Journal: Genes Immun Date: 2011-01-27 Impact factor: 2.676

Phenotypic overlap between infantile systemic lupus erythematosus and Aicardi-Goutières syndrome.

1. Evaluation of the TREX1 gene in a large multi-ancestral lupus cohort.

Review 2. Immunoinflammatory diseases of the central nervous system - the tale of two cytokines.

Review 3. An Update on Autoinflammatory Diseases: Interferonopathies.

4. A Brief Historical Perspective on the Pathological Consequences of Excessive Type I Interferon Exposure In vivo.

5. Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.

6. Exploring Autoimmunity in a Cohort of Children with Genetically Confirmed Aicardi-Goutières Syndrome.

Review 7. Human disease phenotypes associated with mutations in TREX1.

8. Aicardi-Goutières syndrome with emphasis on sonographic features in infancy.

Review 9. New roles for the major human 3'-5' exonuclease TREX1 in human disease.

Review 10. Therapies in Aicardi-Goutières syndrome.