(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

1

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Min Ae Lee-Kirsch

26

object named as

Min Ae Lee-Kirsch

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26 July 2017

4

A Micheil Innes

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26 July 2017

Jürgen Kohlhase

2

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26 July 2017

Christoph Hertzberg

3

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26 July 2017

Kerstin Engel

5

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26 July 2017

Susan Hunger

6

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26 July 2017

Wiktor Borozdin

7

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26 July 2017

Jean K Mah

8

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26 July 2017

Kristina Ungerath

9

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26 July 2017

Hartmut Walkenhorst

10

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26 July 2017

Hans-Helmut Richardt

11

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26 July 2017

Johannes Buckard

12

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26 July 2017

Andrea Bevot

13

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26 July 2017

Corinna Siegel

14

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26 July 2017

Celina von Stülpnagel

15

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26 July 2017

Chrysanthy Ikonomidou

16

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26 July 2017

Kara Thomas

17

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26 July 2017

Virginia Proud

18

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26 July 2017

Frank Niemann

19

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26 July 2017

Dagmar Wieczorek

20

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26 July 2017

Martin Häusler

21

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26 July 2017

Pascal Niggemann

22

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26 July 2017

Volkan Baltaci

23

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26 July 2017

Karsten Conrad

24

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26 July 2017

Pierre Lebon

25

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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

volume

62

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26 July 2017

issue

5

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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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

Type I interferon and lupus

21 January 2018

1 reference

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

21 January 2018

1 reference

Trex1 prevents cell-intrinsic initiation of autoimmunity

21 January 2018

1 reference

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

1 reference

Brain calcification in patients with cerebral lupus.

21 January 2018

1 reference

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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