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7. 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]
9. 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]
10. 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. Rare genetic diseases--new opportunities and challenges through biotechnological progress and scientific knowledge. Fischbach M Eur J Paediatr Neurol; 2002; 6 Suppl A():A71-5; discussion A55-8, A65-6. PubMed ID: 12365364 [No Abstract] [Full Text] [Related]
13. A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis. Aicardi J; Goutières F Ann Neurol; 1984 Jan; 15(1):49-54. PubMed ID: 6712192 [TBL] [Abstract][Full Text] [Related]