Literature DB >> 3239950

Encephalitis among Cree children in northern Quebec.

D N Black1, G V Watters, E Andermann, C Dumont, M E Kabay, P Kaplan, K Meagher-Villemure, J Michaud, G O'Gorman, E Reece.   

Abstract

We report a neurological disease among Cree Indian children in a northern Quebec village. The disease manifests as severe mental retardation, cerebral atrophy with white matter changes and calcifications, and systemic immunological abnormalities. Eleven cases are known in five families. The familial incidence of cases and the high degree of parental consanguinity suggest a genetic contribution. We propose that this entity may be caused by an unusual viral infection in a genetically vulnerable host.

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Year:  1988        PMID: 3239950     DOI: 10.1002/ana.410240402

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  11 in total

Review 1.  Immunoinflammatory diseases of the central nervous system - the tale of two cytokines.

Authors:  M J Hofer; I L Campbell
Journal:  Br J Pharmacol       Date:  2015-06-12       Impact factor: 8.739

2.  The Arg-62 residues of the TREX1 exonuclease act across the dimer interface contributing to catalysis in the opposing protomers.

Authors:  Jason M Fye; Stephanie R Coffin; Clinton D Orebaugh; Thomas Hollis; Fred W Perrino
Journal:  J Biol Chem       Date:  2014-03-09       Impact factor: 5.157

3.  The type I interferon-alpha mediates a more severe neurological disease in the absence of the canonical signaling molecule interferon regulatory factor 9.

Authors:  Markus J Hofer; Wen Li; Sue Ling Lim; Iain L Campbell
Journal:  J Neurosci       Date:  2010-01-20       Impact factor: 6.167

Review 4.  Transgenic models for cytokine-induced neurological disease.

Authors:  Iain L Campbell; Markus J Hofer; Axel Pagenstecher
Journal:  Biochim Biophys Acta       Date:  2009-10-14

Review 5.  The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

Authors:  J L Tolmie; P Shillito; R Hughes-Benzie; J B Stephenson
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

6.  The TREX1 C-terminal region controls cellular localization through ubiquitination.

Authors:  Clinton D Orebaugh; Jason M Fye; Scott Harvey; Thomas Hollis; John C Wilkinson; Fred W Perrino
Journal:  J Biol Chem       Date:  2013-08-26       Impact factor: 5.157

7.  A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21.

Authors:  M Ali; L J Highet; D Lacombe; C Goizet; M D King; U Tacke; M S van der Knaap; L Lagae; C Rittey; H G Brunner; H van Bokhoven; B Hamel; Y A Oade; A Sanchis; I Desguerre; D Cau; N Mathieu; M L Moutard; P Lebon; D Kumar; A P Jackson; Y J Crow
Journal:  J Med Genet       Date:  2005-05-20       Impact factor: 6.318

8.  A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus.

Authors:  Min Ae Lee-Kirsch; Dipanjan Chowdhury; Scott Harvey; Maoliang Gong; Lydia Senenko; Kerstin Engel; Christiane Pfeiffer; Thomas Hollis; Manfred Gahr; Fred W Perrino; Judy Lieberman; Norbert Hubner
Journal:  J Mol Med (Berl)       Date:  2007-04-18       Impact factor: 5.606

Review 9.  Aberrant Type I Interferon Regulation in Autoimmunity: Opposite Directions in MS and SLE, Shaped by Evolution and Body Ecology.

Authors:  Anthony T Reder; Xuan Feng
Journal:  Front Immunol       Date:  2013-09-17       Impact factor: 7.561

10.  Adult mouse eIF2Bε Arg191His astrocytes display a normal integrated stress response in vitro.

Authors:  Lisanne E Wisse; Timo J Ter Braak; Malu-Clair van de Beek; Carola G M van Berkel; Joke Wortel; Vivi M Heine; Chris G Proud; Marjo S van der Knaap; Truus E M Abbink
Journal:  Sci Rep       Date:  2018-02-28       Impact factor: 4.379

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