Literature DB >> 17401526

Late onset vanishing white matter disease.

Axel Riecker, Thomas Nägele, Marco Henneke, Ludger Schöls.   

Abstract

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Year:  2007        PMID： 17401526     DOI： 10.1007/s00415-006-0306-9

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  14 in total

1.  1H chemical shift imaging, MRI, and diffusion-weighted imaging in vanishing white matter disease.

Authors:  Paul E Sijens; Maartje Boon; Linda C Meiners; Oebele F Brouwer; Matthijs Oudkerk
Journal:  Eur Radiol       Date:  2005-04-27       Impact factor: 5.315

Review 2.  Childhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis.

Authors:  Raphael Schiffmann; Orna Elroy-Stein
Journal:  Mol Genet Metab       Date:  2006-01-18       Impact factor: 4.797

3.  EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy.

Authors:  Jörg Dietrich; Michelle Lacagnina; David Gass; Eric Richfield; Margot Mayer-Pröschel; Mark Noble; Carlos Torres; Christoph Pröschel
Journal:  Nat Med       Date:  2005-02-20       Impact factor: 53.440

4.  A new leukoencephalopathy with vanishing white matter.

Authors:  M S van der Knaap; P G Barth; F J Gabreëls; E Franzoni; J H Begeer; H Stroink; J J Rotteveel; J Valk
Journal:  Neurology       Date:  1997-04       Impact factor: 9.910

5.  Heightened stress response in primary fibroblasts expressing mutant eIF2B genes from CACH/VWM leukodystrophy patients.

Authors:  Liraz Kantor; Heather P Harding; David Ron; Raphael Schiffmann; Christine R Kaneski; Scot R Kimball; Orna Elroy-Stein
Journal:  Hum Genet       Date:  2005-10-28       Impact factor: 4.132

6.  Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome.

Authors:  K Wong; R C Armstrong; K A Gyure; A L Morrison; D Rodriguez; R Matalon; A B Johnson; R Wollmann; E Gilbert; T Q Le; C A Bradley; K Crutchfield; R Schiffmann
Journal:  Acta Neuropathol       Date:  2000-12       Impact factor: 17.088

7.  MRI of a family with leukoencephalypathy with vanishing white matter.

Authors:  Elzbieta Jurkiewicz; Hanna Mierzewska; Monika Bekiesińska-Figatowska; Iwona Pakua-Kościesza; Tomasz Kmieć; Gert Scheper; Marjo S van der Knaap; Ewa Pronicka
Journal:  Pediatr Radiol       Date:  2005-05-24

8.  Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

Authors:  P A Leegwater; G Vermeulen; A A Könst; S Naidu; J Mulders; A Visser; P Kersbergen; D Mobach; D Fonds; C G van Berkel; R J Lemmers; R R Frants; C B Oudejans; R B Schutgens; J C Pronk; M S van der Knaap
Journal:  Nat Genet       Date:  2001-12       Impact factor: 38.330

9.  Phenotypic variation in leukoencephalopathy with vanishing white matter.

Authors:  M S van der Knaap; W Kamphorst; P G Barth; C L Kraaijeveld; E Gut; J Valk
Journal:  Neurology       Date:  1998-08       Impact factor: 9.910

10.  Arg113His mutation in eIF2Bepsilon as cause of leukoencephalopathy in adults.

Authors:  M S van der Knaap; P A J Leegwater; C G M van Berkel; C Brenner; E Storey; M Di Rocco; F Salvi; J C Pronk
Journal:  Neurology       Date:  2004-05-11       Impact factor: 9.910
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  2 in total

Review 1.  [Demyelinating disorders].

Authors:  T Weber; W Köhler
Journal:  Nervenarzt       Date:  2010-04       Impact factor: 1.214

2.  Adult-onset vanishing white matter disease with the EIF2B2 gene mutation presenting as menometrorrhagia.

Authors:  Cuibai Wei; Qi Qin; Fei Chen; Aihong Zhou; Fen Wang; Xiumei Zuo; Rong Chen; Jihui Lyu; Jianping Jia
Journal:  BMC Neurol       Date:  2019-08-22       Impact factor: 2.474
  2 in total

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