Literature DB >> 27086608

Aicardi-Goutières Syndrome.

Rashid Merchant1, Mitusha Verma2, Ami Shah3, Shilpa Kulkarni3, Anil Jalan4.   

Abstract

Mesh：

Year:  2016        PMID： 27086608     DOI： 10.1007/s12098-016-2104-4

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Interferon and Aicardi-Goutières syndrome.

Authors:  Pierre Lebon; Jean François Meritet; Anne Krivine; Flore Rozenberg
Journal:  Eur J Paediatr Neurol       Date:  2002       Impact factor: 3.140

2.  Aicardi-Goutieres syndrome: neuroradiologic findings and follow-up.

Authors:  C Uggetti; R La Piana; S Orcesi; M G Egitto; Y J Crow; E Fazzi
Journal:  AJNR Am J Neuroradiol       Date:  2009-07-23       Impact factor: 3.825

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

Authors:  J Aicardi; F Goutières
Journal:  Ann Neurol       Date:  1984-01       Impact factor: 10.422

4.  Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype.

Authors:  N Blau; L Bonafé; I Krägeloh-Mann; B Thöny; L Kierat; M Häusler; V Ramaekers
Journal:  Neurology       Date:  2003-09-09       Impact factor: 9.910

5.  Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

Authors:  Gillian Rice; Teresa Patrick; Rekha Parmar; Claire F Taylor; Alec Aeby; Jean Aicardi; Rafael Artuch; Simon Attard Montalto; Carlos A Bacino; Bruno Barroso; Peter Baxter; Willam S Benko; Carsten Bergmann; Enrico Bertini; Roberta Biancheri; Edward M Blair; Nenad Blau; David T Bonthron; Tracy Briggs; Louise A Brueton; Han G Brunner; Christopher J Burke; Ian M Carr; Daniel R Carvalho; Kate E Chandler; Hans-Jurgen Christen; Peter C Corry; Frances M Cowan; Helen Cox; Stefano D'Arrigo; John Dean; Corinne De Laet; Claudine De Praeter; Catherine Dery; Colin D Ferrie; Kim Flintoff; Suzanna G M Frints; Angels Garcia-Cazorla; Blanca Gener; Cyril Goizet; Francoise Goutieres; Andrew J Green; Agnes Guet; Ben C J Hamel; Bruce E Hayward; Arvid Heiberg; Raoul C Hennekam; Marie Husson; Andrew P Jackson; Rasieka Jayatunga; Yong-Hui Jiang; Sarina G Kant; Amy Kao; Mary D King; Helen M Kingston; Joerg Klepper; Marjo S van der Knaap; Andrew J Kornberg; Dieter Kotzot; Wilfried Kratzer; Didier Lacombe; Lieven Lagae; Pierre Georges Landrieu; Giovanni Lanzi; Andrea Leitch; Ming J Lim; John H Livingston; Charles M Lourenco; E G Hermione Lyall; Sally A Lynch; Michael J Lyons; Daphna Marom; John P McClure; Robert McWilliam; Serge B Melancon; Leena D Mewasingh; Marie-Laure Moutard; Ken K Nischal; John R Ostergaard; Julie Prendiville; Magnhild Rasmussen; R Curtis Rogers; Dominique Roland; Elisabeth M Rosser; Kevin Rostasy; Agathe Roubertie; Amparo Sanchis; Raphael Schiffmann; Sabine Scholl-Burgi; Sunita Seal; Stavit A Shalev; C Sierra Corcoles; Gyan P Sinha; Doriette Soler; Ronen Spiegel; John B P Stephenson; Uta Tacke; Tiong Yang Tan; Marianne Till; John L Tolmie; Pam Tomlin; Federica Vagnarelli; Enza Maria Valente; Rudy N A Van Coster; Nathalie Van der Aa; Adeline Vanderver; Johannes S H Vles; Thomas Voit; Evangeline Wassmer; Bernhard Weschke; Margo L Whiteford; Michel A A Willemsen; Andreas Zankl; Sameer M Zuberi; Simona Orcesi; Elisa Fazzi; Pierre Lebon; Yanick J Crow
Journal:  Am J Hum Genet       Date:  2007-09-04       Impact factor: 11.025
  5 in total
  1 in total

1.  Type I interferonopathies with novel compound heterozygous TREX1 mutations in two siblings with different symptoms responded to tofacitinib.

Authors:  Shiyu Zhang; Jiaxing Song; Yuyan Yang; Huilei Miao; Lu Yang; Yuehua Liu; Xue Zhang; Yaping Liu; Tao Wang
Journal:  Pediatr Rheumatol Online J       Date:  2021-01-06       Impact factor: 3.054
  1 in total

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