Literature DB >> 11601505

Myelinopathia centralis diffusa (vanishing white matter disease): evidence of apoptotic oligodendrocyte degeneration in early lesion development.

W Brück1, J Herms, K Brockmann, W Schulz-Schaeffer, F Hanefeld.   

Abstract

We describe histopathological changes in a 2-year-old boy who died from myelinopathia centralis diffusa. Despite extensive white matter destruction, surprisingly high numbers of oligodendrocytes expressing proteolipid protein mRNA were detected. In an active demyelinating lesion in the brainstem, oligodendrocytes showed typical signs of apoptosis. We suggest that death of mature oligodendrocytes is the critical event in the disease.

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Year:  2001        PMID: 11601505     DOI: 10.1002/ana.1227

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


  12 in total

1.  Ovarian failure related to eukaryotic initiation factor 2B mutations.

Authors:  Anne Fogli; Diana Rodriguez; Eléonore Eymard-Pierre; Françoise Bouhour; Pierre Labauge; Brandon F Meaney; Susan Zeesman; Christine R Kaneski; Raphael Schiffmann; Odile Boespflug-Tanguy
Journal:  Am J Hum Genet       Date:  2003-04-21       Impact factor: 11.025

2.  Hereditary diffuse leukoencephalopathy with spheroids: ultrastructural and immunoelectron microscopic studies.

Authors:  Wen-Lang Lin; Zbigniew K Wszolek; Dennis W Dickson
Journal:  Int J Clin Exp Pathol       Date:  2010-07-26

3.  Defective glial maturation in vanishing white matter disease.

Authors:  Marianna Bugiani; Ilja Boor; Barbara van Kollenburg; Nienke Postma; Emiel Polder; Carola van Berkel; Ronald E van Kesteren; Martha S Windrem; Elly M Hol; Gert C Scheper; Steven A Goldman; Marjo S van der Knaap
Journal:  J Neuropathol Exp Neurol       Date:  2011-01       Impact factor: 3.685

4.  eIF2B-related disorders: antenatal onset and involvement of multiple organs.

Authors:  Marjo S van der Knaap; Carola G M van Berkel; Jochen Herms; Rudy van Coster; Martina Baethmann; Sakkubai Naidu; Eugen Boltshauser; Michèl A A P Willemsen; Barbara Plecko; Georg F Hoffmann; Christopher G Proud; Gert C Scheper; Jan C Pronk
Journal:  Am J Hum Genet       Date:  2003-10-17       Impact factor: 11.025

5.  An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous region.

Authors:  Yukiko Hata; Koshi Kinoshita; Kazushi Miya; Keiichi Hirono; Fukiko Ichida; Koji Yoshida; Naoki Nishida
Journal:  Int J Clin Exp Pathol       Date:  2014-05-15

Review 6.  Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms.

Authors:  Marjo S van der Knaap; Marianna Bugiani
Journal:  Acta Neuropathol       Date:  2017-06-21       Impact factor: 17.088

7.  Axonal abnormalities in vanishing white matter.

Authors:  Melanie D Klok; Marianna Bugiani; Sharon I de Vries; Wouter Gerritsen; Marjolein Breur; Sophie van der Sluis; Vivi M Heine; Maarten H P Kole; Wia Baron; Marjo S van der Knaap
Journal:  Ann Clin Transl Neurol       Date:  2018-03-01       Impact factor: 4.511

8.  Pathoetiology of multiple sclerosis: are we barking up the wrong tree?

Authors:  Peter K Stys
Journal:  F1000Prime Rep       Date:  2013-06-03

Review 9.  Diagnosis of inflammatory demyelination in biopsy specimens: a practical approach.

Authors:  Tanja Kuhlmann; Hans Lassmann; Wolfgang Brück
Journal:  Acta Neuropathol       Date:  2008-01-04       Impact factor: 17.088

Review 10.  Inherited and acquired disorders of myelin: The underlying myelin pathology.

Authors:  Ian D Duncan; Abigail B Radcliff
Journal:  Exp Neurol       Date:  2016-04-09       Impact factor: 5.330

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