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3. The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis). Tolmie JL; Shillito P; Hughes-Benzie R; Stephenson JB J Med Genet; 1995 Nov; 32(11):881-4. PubMed ID: 8592332 [TBL] [Abstract][Full Text] [Related]
4. Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy. Orcesi S; Pessagno A; Biancheri R; La Piana R; Mascaretti M; Rossi A; Rice GI; Crow YJ; Fazzi E; Veneselli E Eur J Paediatr Neurol; 2008 Sep; 12(5):408-11. PubMed ID: 18069026 [TBL] [Abstract][Full Text] [Related]
5. [Aicardi-Goutieres syndrome: an oft unrecognised familial early-onset encephalopathy]. San Antonio V; Sachs P; Monier A; Aicardi J; Evrard P; Arzimanoglou A Rev Neurol (Paris); 2005 Apr; 161(4):445-50. PubMed ID: 15924080 [TBL] [Abstract][Full Text] [Related]
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7. Encephalopathy of infancy with intracerebral calcification and chronic spinal fluid lymphocytosis--another case of the Aicardi-Goutières syndrome. Bönnemann CG; Meinecke P Neuropediatrics; 1992 Jun; 23(3):157-61. PubMed ID: 1641084 [TBL] [Abstract][Full Text] [Related]
8. Aicardi-Goutières syndrome: an expanding phenotype. McEntagart M; Kamel H; Lebon P; King MD Neuropediatrics; 1998 Jun; 29(3):163-7. PubMed ID: 9706629 [TBL] [Abstract][Full Text] [Related]
9. A case of progressive familial encephalopathy in infancy with calcification of the basal ganglia and chronic cerebrospinal fluid lymphocytosis. Giroud M; Gouyon JB; Chaumet F; Cinquin AM; Chevalier-Nivelon A; Alison M; Dumas R Childs Nerv Syst; 1986; 2(1):47-8. PubMed ID: 3731164 [TBL] [Abstract][Full Text] [Related]
10. Aicardi-Goutières syndrome: an update and results of interferon-alpha studies. Goutières F; Aicardi J; Barth PG; Lebon P Ann Neurol; 1998 Dec; 44(6):900-7. PubMed ID: 9851434 [TBL] [Abstract][Full Text] [Related]
11. Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype. Blau N; Bonafé L; Krägeloh-Mann I; Thöny B; Kierat L; Häusler M; Ramaekers V Neurology; 2003 Sep; 61(5):642-7. PubMed ID: 12963755 [TBL] [Abstract][Full Text] [Related]
12. Atypical case of Aicardi-Goutières syndrome with late-onset myoclonic status. Berger A; Schroeter C; Wiemer-Kruel A; Strobl K; Hoffmann GF; Rating D; Lebon P; Ernst JP; Wolf NI Epileptic Disord; 2007 Jun; 9(2):140-4. PubMed ID: 17525022 [TBL] [Abstract][Full Text] [Related]
13. Lack of progression of brain atrophy in Aicardi-Goutières syndrome. Polizzi A; Pavone P; Parano E; Incorpora G; Ruggieri M Pediatr Neurol; 2001 Apr; 24(4):300-2. PubMed ID: 11377106 [TBL] [Abstract][Full Text] [Related]
14. Aicardi-Goutières syndrome presenting with haematemesis in infancy. Hall D; Rice GI; Akbar N; Meager A; Crow YJ; Lim MJ Acta Paediatr; 2009 Dec; 98(12):2005-8. PubMed ID: 19775308 [TBL] [Abstract][Full Text] [Related]
15. Brainstem lesion in Aicardi-Goutières syndrome. Kato M; Ishii R; Honma A; Ikeda H; Hayasaka K Pediatr Neurol; 1998 Aug; 19(2):145-7. PubMed ID: 9744637 [TBL] [Abstract][Full Text] [Related]
16. Aicardi-Goutières syndrome: a genetic microangiopathy? Barth PG; Walter A; van Gelderen I Acta Neuropathol; 1999 Aug; 98(2):212-6. PubMed ID: 10442562 [TBL] [Abstract][Full Text] [Related]
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