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6. Recognizable inherited syndrome of progressive central nervous system degeneration and generalized intracranial calcification with overlapping phenotype of the syndrome of Aicardi and Goutières. Kumar D; Rittey C; Cameron AH; Variend S Am J Med Genet; 1998 Feb; 75(5):508-15. PubMed ID: 9489795 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Aicardi-Goutières syndrome: description of a late onset case. D'Arrigo S; Riva D; Bulgheroni S; Chiapparini L; Lebon P; Rice G; Crow YJ; Pantaleoni C Dev Med Child Neurol; 2008 Aug; 50(8):631-4. PubMed ID: 18754903 [TBL] [Abstract][Full Text] [Related]
9. Respiratory chain deficiency in a female with Aicardi-Goutières syndrome. Barnérias C; Giurgea I; Hertz-Pannier L; Bahi-Buisson N; Boddaert N; Rustin P; Rotig A; Desguerre I; Munnich A; de Lonlay P Dev Med Child Neurol; 2006 Mar; 48(3):227-30. PubMed ID: 16483401 [TBL] [Abstract][Full Text] [Related]
11. Aicardi-Goutières syndrome: a description of 21 new cases and a comparison with the literature. Lanzi G; Fazzi E; D'Arrigo S Eur J Paediatr Neurol; 2002; 6 Suppl A():A9-22; discussion A23-5, A77-86. PubMed ID: 12365365 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Interferon-related transcriptome alterations in the cerebrospinal fluid cells of Aicardi-Goutières patients. Izzotti A; Pulliero A; Orcesi S; Cartiglia C; Longobardi MG; Capra V; Lebon P; Cama A; La Piana R; Lanzi G; Fazzi E Brain Pathol; 2009 Oct; 19(4):650-60. PubMed ID: 19016741 [TBL] [Abstract][Full Text] [Related]
14. Blueberry muffin rash as the presenting sign of Aicardi-Goutières syndrome. Brisman S; Gonzalez M; Morel KD Pediatr Dermatol; 2009; 26(4):432-5. PubMed ID: 19689519 [TBL] [Abstract][Full Text] [Related]
15. 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]
17. 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]
18. Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism. Crow YJ; Black DN; Ali M; Bond J; Jackson AP; Lefson M; Michaud J; Roberts E; Stephenson JB; Woods CG; Lebon P J Med Genet; 2003 Mar; 40(3):183-7. PubMed ID: 12624136 [TBL] [Abstract][Full Text] [Related]
19. [Aicardi-Goutières syndrome: report of two new cases]. Blanco-Barca MO; Curros Novo MC; Alvarez Moreno A; Alonso Martín A; Eirís-Puñal JM; Castro-Gago M An Pediatr (Barc); 2005 Feb; 62(2):166-70. PubMed ID: 15701315 [TBL] [Abstract][Full Text] [Related]
20. The genetics of Aicardi-Goutières syndrome. Crow Y Eur J Paediatr Neurol; 2002; 6 Suppl A():A33-5; discussion A37-9, A77-86. PubMed ID: 12365359 [No Abstract] [Full Text] [Related] [Next] [New Search]