Paediatric neurology: brain development at an interface between genetics, the environment, and the immune system

The Lancet Neurology

Volumn 9, Issue 1, 2010, Pages 13-14

  Tardieu, Marc ^a  

^a BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA INTERFERON; CYCLOPHOSPHAMIDE; GLYCOPROTEIN; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; PROTEIN RANBP2; PROTEIN RNASET2; RAN PROTEIN; RITUXIMAB; STEROID; UNCLASSIFIED DRUG;

AICARDI GOUTIERES SYNDROME; ANGIOGENESIS; ARTICLE; BRAIN DEVELOPMENT; BRAIN INFECTION; CELL COUNT; CEREBROSPINAL FLUID ANALYSIS; CYTOMEGALOVIRUS INFECTION; DISEASE PREDISPOSITION; GENE MUTATION; GENETIC DISORDER; GENETIC RISK; HEREDITY; HERPES SIMPLEX ENCEPHALITIS; LOSS OF FUNCTION MUTATION; NERVE CELL; NUCLEAR MAGNETIC RESONANCE IMAGING; OPSOCLONUS MYOCLONUS SYNDROME; PRIORITY JOURNAL; PROTEIN CEREBROSPINAL FLUID LEVEL; RNA METABOLISM; SEROCONVERSION; VIRUS ENCEPHALITIS;

EID: 72049093207     PISSN: 14744422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1474-4422(09)70307-2     Document Type: Note

References (12)

1. Mizuguchi M. Acute necrotizing encephalopathy of childhood: a novel form of acute encephalopathy prevalent in Japan and Taiwan. Brain Dev 19 (1997) 82-92
2. Neilson D.E., Adams M.D., Orr C.M.D., et al. Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore RANBP2. Am J Hum Genet 84 (2009) 44-51
3. Alcais A., Abel L., and Casanova J.L. Human genetics of infectious diseases: between proof of principle and paradigm. J Clin Invest 119 (2009) 2506-2514
4. Sancho-Shimizu V., Zhang S.Y., Abel L., et al. Genetic susceptibility to herpes simplex 1 encephalitis in mice and human. Curr Opin Allergy Clin Immunol 7 (2007) 495-505
5. Zhang S.-Y., Jouanguy E., Ugolini S., et al. TLR3 deficiency in otherwise healthy patients with herpes simplex encephalitis. Science 317 (2007) 522-527
6. Henneke M., Diekmann S., Ohlenbusch A., et al. RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection. Nat Genet 41 (2009) 773-775
7. Crow Y.J., Leitch A., Hayward B.E., et al. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. Nat Genet 38 (2006) 910-916
8. Rice G.I., Bond J., Asipu A., et al. Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet 41 (2009) 829-833
9. Florance N.R., Davis R.L., Lam C., et al. Anti-N-methyl-D-aspartate receptor encephalitis in children and adolescent. Ann Neurol 66 (2009) 11-18
10. Dale R.C., Irani S.R., Brilot F., et al. NMDA receptor antibodies in pediatric dyskinetic encephalitis lethargica. Ann Neurol 66 (2009) 704-709
11. Lebas, Husson B., Didelot A., et al. Expanding spectrum of encephalitis with NMDA receptor in young children. J Child Neurol (2009) 10.1177/0883073809343319 published online Oct 15.
12. Dalmau J., Tuzun E., Wu H.Y., et al. Paraneoplastic anti-N-methyl-D aspartate receptor encephalitis associated with ovarian teratoma. Ann Neurol 61 (2007) 25-36