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4. 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]
5. 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]
6. 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]
16. 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]
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18. A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21. Ali M; Highet LJ; Lacombe D; Goizet C; King MD; Tacke U; van der Knaap MS; Lagae L; Rittey C; Brunner HG; van Bokhoven H; Hamel B; Oade YA; Sanchis A; Desguerre I; Cau D; Mathieu N; Moutard ML; Lebon P; Kumar D; Jackson AP; Crow YJ J Med Genet; 2006 May; 43(5):444-50. PubMed ID: 15908569 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Case of Aicardi-Goutières syndrome with long-lasting increase of cerebrospinal interferon-alpha. Dimova PS; Mikova OA J Child Neurol; 2005 Nov; 20(11):915-9. PubMed ID: 16417864 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]