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366 related items for PubMed ID: 19689519
1. 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 [Abstract] [Full Text] [Related]
5. 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]
6. 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]
13. Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder? Fazzi E, Cattalini M, Orcesi S, Tincani A, Andreoli L, Balottin U, De Simone M, Fredi M, Facchetti F, Galli J, Giliani S, Izzotti A, Meini A, Olivieri I, Plebani A. Autoimmun Rev; 2013 Feb 28; 12(4):506-9. PubMed ID: 22940555 [Abstract] [Full Text] [Related]
14. 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 28; 32(11):881-4. PubMed ID: 8592332 [Abstract] [Full Text] [Related]
15. Blueberry muffin rash secondary to hereditary spherocytosis. Daum LM, Sklar LR, Mehregan DR. Cutis; 2018 Feb 28; 101(2):111-114. PubMed ID: 29554165 [Abstract] [Full Text] [Related]
17. 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 28; 23(3):157-61. PubMed ID: 1641084 [Abstract] [Full Text] [Related]