Literature DB >> 30315562

A Review of Infantile Vanishing White Matter Disease and A New Mutation.

Halûk Yavuz1.   

Abstract

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Mesh：

Year:  2017        PMID： 30315562

Source DB:  PubMed          Journal:  Acta Neurol Taiwan        ISSN： 1028-768X


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  4 in total

1.  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.  Familial deep cavitating state with a glutathione metabolism defect.

Authors:  Julien Fauré; Gérard Besson; John Rendu; Laetitia Van Noolen; Catherine Garrel; Julie Brocard; Isabelle Marty; Christelle Corne
Journal:  Ann Clin Transl Neurol       Date:  2019-11-09       Impact factor: 4.511

3.  EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report.

Authors:  Ilaria Filareto; Giulia Cinelli; Ilaria Scalabrini; Elisa Caramaschi; Patrizia Bergonzini; Elisabetta Spezia; Alessandra Todeschini; Lorenzo Iughetti
Journal:  Ital J Pediatr       Date:  2022-07-27       Impact factor: 3.288

4.  Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease.

Authors:  Doeun Kim; Yu-Ri Lee; Tae-Ik Choi; Se-Hee Kim; Hoon-Chul Kang; Cheol-Hee Kim; Sangkyu Lee
Journal:  Int J Mol Sci       Date:  2021-03-08       Impact factor: 5.923
  4 in total

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