Aicardi–Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies

Brain-Reactive Antibodies and Disease

(2013) B. Diamond et al.   Annual Review of Immunology

Therapies in Aicardi-Goutières syndrome

(2013) Y. J. Crow et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

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

(2013) I Olivieri et al.   LUPUS

Aquaporin water channels in the nervous system

(2013) Marios C. Papadopoulos et al.   NATURE REVIEWS NEUROSCIENCE

B cell encounters with apoptotic cells

(2012) Isabelle Bekeredjian-Ding   AUTOIMMUNITY

Antinuclear antibody detection by automated multiplex immunoassay in untreated patients at the time of diagnosis

(2012) Katrijn Op De Beéck et al.   AUTOIMMUNITY REVIEWS

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

(2012) Elisa Fazzi et al.   AUTOIMMUNITY REVIEWS

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

(2012) Gillian I Rice et al.   NATURE GENETICS

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

(2011) Kazunori Nanri et al.   Diagnostic Pathology

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

(2011) B Namjou et al.   GENES AND IMMUNITY

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

(2011) B. Xin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

(2010) Jane C. Ravenscroft et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

(2010) Georgia Ramantani et al.   ARTHRITIS AND RHEUMATISM

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

(2010) VENKATESWARAN RAMESH et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

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

(2010) Holger Thiele et al.   HUMAN MUTATION

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

(2010) Shahrooz Rashtak et al.   JOURNAL OF NEUROIMMUNOLOGY

Aicardi-Goutieres syndrome

(2009) S. Orcesi et al.   BRITISH MEDICAL BULLETIN

Aicardi-Goutières syndrome: an important Mendelian mimic of congenital infection

(2009) Yanick J Crow et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

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

(2009) Y. J. Crow et al.   HUMAN MOLECULAR GENETICS

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

(2009) DS Domiciano et al.   LUPUS

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

(2009) Gillian I Rice et al.   NATURE GENETICS

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

(2008) S. Orcesi et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

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

(2008) Jane T. Van Heteren et al.   GLIA

Cutaneous histopathological findings of AicardiGoutires syndrome, overlap with chilblain lupus

(2008) Athanassios Kolivras et al.   JOURNAL OF CUTANEOUS PATHOLOGY