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147 related items for PubMed ID: 15701315
1. [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 [Abstract] [Full Text] [Related]
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 [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 [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 [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 Apr; 6 Suppl A():A9-22; discussion A23-5, A77-86. PubMed ID: 12365365 [Abstract] [Full Text] [Related]
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 [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 [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 Jun; 2(1):47-8. PubMed ID: 3731164 [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 [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 [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 [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 [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 [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 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
18. TREX-1 related Aicardi-Goutières syndrome improved by Janus kinase inhibitor. Ryckmans C, Donge M, Marchèse A, Mastouri M, Thomee C, Stouffs K, Lieser SL, Scalais E. Am J Med Genet A; 2024 May; 194(5):e63510. PubMed ID: 38135344 [Abstract] [Full Text] [Related]