Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome (Q33388122)

26 July 2017

title

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

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26 July 2017

Georgia Ramantani

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Min Ae Lee-Kirsch

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26 July 2017

A Micheil Innes

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26 July 2017

Jürgen Kohlhase

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26 July 2017

Christoph Hertzberg

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26 July 2017

Kerstin Engel

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26 July 2017

Susan Hunger

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26 July 2017

Wiktor Borozdin

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26 July 2017

Jean K Mah

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26 July 2017

Kristina Ungerath

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26 July 2017

Hartmut Walkenhorst

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26 July 2017

Hans-Helmut Richardt

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26 July 2017

Johannes Buckard

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26 July 2017

Andrea Bevot

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26 July 2017

Corinna Siegel

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26 July 2017

Celina von Stülpnagel

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26 July 2017

Chrysanthy Ikonomidou

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26 July 2017

Kara Thomas

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26 July 2017

Virginia Proud

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26 July 2017

Frank Niemann

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26 July 2017

Dagmar Wieczorek

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26 July 2017

Martin Häusler

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26 July 2017

Pascal Niggemann

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26 July 2017

Volkan Baltaci

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26 July 2017

Karsten Conrad

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26 July 2017

Pierre Lebon

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26 July 2017

language of work or name

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1 May 2010

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26 July 2017

published in

Arthritis & Rheumatology

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

1469-1477

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

26 July 2017

cites work

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Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy

21 January 2018

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

21 January 2018

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The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

21 January 2018

1 reference

Familial systemic lupus erythematosus and congenital infection-like syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus

21 January 2018

1 reference

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

21 January 2018

1 reference

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

The emerging role of interferon in human systemic lupus erythematosus

21 January 2018

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Type I interferon and lupus

21 January 2018

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Trex1 exonuclease degrades ssDNA to prevent chronic checkpoint activation and autoimmune disease

21 January 2018

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Trex1 prevents cell-intrinsic initiation of autoimmunity

21 January 2018

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

21 January 2018

1 reference

Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new cases.

21 January 2018

1 reference

The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patients

21 January 2018

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Brain calcification in patients with cerebral lupus

21 January 2018

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Quantitative magnetic resonance imaging analyses and clinical significance of hyperintense white matter lesions in systemic lupus erythematosus patients

21 January 2018

1 reference

Imaging modalities in central nervous system systemic lupus erythematosus

21 January 2018

1 reference

The 1982 revised criteria for the classification of systemic lupus erythematosus

21 January 2018

1 reference

Familial chilblain lupus--a monogenic form of cutaneous lupus erythematosus due to a heterozygous mutation in TREX1.

21 January 2018

1 reference

Identification and expression of the TREX1 and TREX2 cDNA sequences encoding mammalian 3'-->5' exonucleases

21 January 2018

1 reference

Genetics of autoimmune diseases--disorders of immune homeostasis

21 January 2018

1 reference

A proposed classification of the immunological diseases

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ART.27367

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26 July 2017

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