Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies. (Q48728863)

15 February 2018

title

Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies. (English)

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Yanick J. Crow

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Adeline Vanderver

object named as

Adeline Vanderver

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Eleonora Aronica

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object named as

Eleonora Aronica

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Taco W Kuijpers

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author name string

Eloy Cuadrado

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Kristy J Brown

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Annie Sandza

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Asako Takanohashi

5

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Machiel H Jansen

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Jasper Anink

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Brian Herron

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Simona Orcesi

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Ivana Olivieri

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Pierre Lebon

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Elly M Hol

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language of work or name

English

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publication date

6 June 2014

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Annals of the Rheumatic Diseases

published in

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volume

74

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issue

10

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page(s)

1931-1939

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15 February 2018

A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

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Aicardi-Goutières syndrome: an update and results of interferon-alpha studies

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Aicardi-Goutières syndrome: a description of 21 new cases and a comparison with the literature.

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Aicardi-Goutières syndrome

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Aicardi-Goutieres syndrome.

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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

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Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

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Clinical and molecular phenotype of Aicardi-Goutieres syndrome

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Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome

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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

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Aicardi-Goutieres syndrome and related phenotypes: linking nucleic acid metabolism with autoimmunity

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Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?

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

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Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome

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Autosomal dominant inheritance of a heterozygous mutation in SAMHD1 causing familial chilblain lupus

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Astrocytes produce interferon-alpha and CXCL10, but not IL-6 or CXCL8, in Aicardi-Goutières syndrome

21 January 2018

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Cerebral thrombotic microangiopathy and antiphospholipid antibodies in Aicardi-Goutieres syndrome--report of two sisters.

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Identification of autoantibody clusters that best predict lupus disease activity using glomerular proteome arrays

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Genesis: cluster analysis of microarray data

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Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome?

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Familial systemic lupus erythematosus and congenital infection-like syndrome

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Serology of celiac disease in gluten-sensitive ataxia or neuropathy: role of deamidated gliadin antibody

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Immune cross-reactivity in celiac disease: anti-gliadin antibodies bind to neuronal synapsin I.

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Selective loss of Purkinje cells in a patient with anti-gliadin-antibody-positive autoimmune cerebellar ataxia

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Aicardi-Goutières syndrome: a genetic microangiopathy?

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Pathogenic role of anti-endothelial cell antibodies in autoimmune rheumatic diseases

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A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis

21 January 2018

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IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel

21 January 2018

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Aquaporin water channels in the nervous system.

21 January 2018

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Brain-reactive antibodies and disease.

21 January 2018

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Mimicry and autoantibody-mediated neuronal cell signaling in Sydenham chorea.

21 January 2018

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Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke

21 January 2018

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Cerebral arterial stenoses and stroke: novel features of Aicardi-Goutières syndrome caused by the Arg164X mutation in SAMHD1 are associated with altered cytokine expression

21 January 2018

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Dysregulation of the immune system in Aicardi-Goutières syndrome: another example in a TREX1-mutated patient.

21 January 2018

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Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy.

21 January 2018

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Aicardi-Goutières syndrome: immunophenotyping in relation to interferon-alpha

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21 January 2018

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Cutaneous histopathological findings of AicardiGoutires syndrome, overlap with chilblain lupus

21 January 2018

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Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis

21 January 2018

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10.1136/ANNRHEUMDIS-2014-205396

21 January 2018

Identifiers

DOI

1 reference

15 February 2018

PubMed ID

24906636

1 reference

15 February 2018