Literature DB >> 27613634

Cerebral involvement in mitochondrial disorders on imaging.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

Entities:  

Keywords:  Central nervous system; Gene; Imaging; Maternal inheritance; Mitochondrial; Mutation; mtDNA

Mesh：

Substances：

Year:  2016        PMID： 27613634     DOI： 10.1007/s00381-016-3241-9

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN： 0256-7040            Impact factor:   1.475


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  5 in total

Review 1.  Mitochondrial vasculopathy.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  World J Cardiol       Date:  2016-05-26

2.  Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption.

Authors:  H L M van Straaten; J P van Tintelen; J M F Trijbels; L P van den Heuvel; D Troost; J M Rozemuller; M Duran; L S de Vries; M Schuelke; P G Barth
Journal:  Neuropediatrics       Date:  2005-06       Impact factor: 1.947

3.  A3243G mitochondrial mutation associated with polymicrogyria.

Authors:  W T Keng; D T Pilz; B Minns; D R FitzPatrick
Journal:  Dev Med Child Neurol       Date:  2003-10       Impact factor: 5.449

Review 4.  The many faces of paediatric mitochondrial disease on neuroimaging.

Authors:  Fabian Baertling; Dirk Klee; Tobias B Haack; Holger Prokisch; Thomas Meitinger; Ertan Mayatepek; Jörg Schaper; Felix Distelmaier
Journal:  Childs Nerv Syst       Date:  2016-07-23       Impact factor: 1.475

Review 5.  Central nervous system imaging in mitochondrial disorders.

Authors:  Josef Finsterer
Journal:  Can J Neurol Sci       Date:  2009-03       Impact factor: 2.104
  5 in total
  1 in total

Review 1.  Cerebral imaging in paediatric mitochondrial disorders.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Neuroradiol J       Date:  2018-07-06
  1 in total

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