Literature DB >> 20349030

[Demyelinating disorders].

T Weber1, W Köhler.   

Abstract

Leukoencephalopathies in adults are frequent and exhibit highly variable aetiology, including multiple acquired causes such as inflammatory, vascular or toxic diseases and neoplasias. In contrast leukodystrophies are genetically determined, chronic progressive myelin disorders with a variable pathogenetic background and a great diversity of clinical and paraclinical findings. Some diseases, namely those with an additional inborn error of metabolism, are treatable. Genetic counselling appears to be of major importance for patients and their families. In the light of numerous acquired adulthood leukoencephalopathies a clear delineation of late-onset genetic leukodystrophies is necessary. Clinical symptoms and MRI patterns of some of the major leukodystrophies are reported, including possibilities of biochemical and genetic testing.

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Year:  2010        PMID: 20349030     DOI: 10.1007/s00115-010-2948-1

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  114 in total

1.  Asymptomatic spinal cord involvement in posterior reversible encephalopathy syndrome.

Authors:  C Briganti; M Caulo; F Notturno; A Tartaro; A Uncini
Journal:  Neurology       Date:  2009-11-03       Impact factor: 9.910

2.  Heterogeneity of multiple sclerosis lesions: implications for the pathogenesis of demyelination.

Authors:  C Lucchinetti; W Brück; J Parisi; B Scheithauer; M Rodriguez; H Lassmann
Journal:  Ann Neurol       Date:  2000-06       Impact factor: 10.422

3.  Atypical progressive multifocal leukoencephalopathy associated with an unusual JC polyomavirus mutation.

Authors:  Emma C Tallantyre; Simon M L Paine; Colin P Sharp; James S Lowe; Bruno Gran
Journal:  Arch Neurol       Date:  2009-08

Review 4.  Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC).

Authors:  R Blattner; A Von Moers; P A J Leegwater; F A Hanefeld; M S Van Der Knaap; W Köhler
Journal:  Neuropediatrics       Date:  2003-08       Impact factor: 1.947

5.  Cerebral blindness and encephalopathy with cyclosporin A toxicity.

Authors:  A M Rubin; H Kang
Journal:  Neurology       Date:  1987-06       Impact factor: 9.910

6.  A case of hypertensive encephalopathy with extensive spinal lesions on MRI.

Authors:  Masako Nagato; Yasuo Takahashi; Mieko Yoshioka; Mitsuhiko Nambu
Journal:  Brain Dev       Date:  2009-09-05       Impact factor: 1.961

7.  Progressive multifocal leukoencephalopathy after natalizumab monotherapy.

Authors:  Hans Lindå; Anders von Heijne; Eugene O Major; Caroline Ryschkewitsch; Johan Berg; Tomas Olsson; Claes Martin
Journal:  N Engl J Med       Date:  2009-09-10       Impact factor: 91.245

Review 8.  From the archives of the AFIP: central nervous system infections associated with human immunodeficiency virus infection: radiologic-pathologic correlation.

Authors:  Alice B Smith; James G Smirniotopoulos; Elisabeth J Rushing
Journal:  Radiographics       Date:  2008 Nov-Dec       Impact factor: 5.333

9.  IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel.

Authors:  Vanda A Lennon; Thomas J Kryzer; Sean J Pittock; A S Verkman; Shannon R Hinson
Journal:  J Exp Med       Date:  2005-08-08       Impact factor: 14.307

Review 10.  Leukoencephalopathies associated with inborn errors of metabolism in adults.

Authors:  F Sedel; A Tourbah; B Fontaine; C Lubetzki; N Baumann; J-M Saudubray; O Lyon-Caen
Journal:  J Inherit Metab Dis       Date:  2008-02-25       Impact factor: 4.750

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