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Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.

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Title: Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
Authors: Demarest ST; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Whitehead MT; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Turnacioglu S; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA., Pearl PL; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA., Gropman AL; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA AGropman@childrensnational.org.
Source: Journal of child neurology [J Child Neurol] 2014 Sep; Vol. 29 (9), pp. 1249-56. Date of Electronic Publication: 2014 Jul 17.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Sage Country of Publication: United States NLM ID: 8606714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1708-8283 (Electronic) Linking ISSN: 08830738 NLM ISO Abbreviation: J Child Neurol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
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  Data: <searchLink fieldCode="AU" term="%22Demarest+ST%22">Demarest ST</searchLink>; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA.<br /><searchLink fieldCode="AU" term="%22Whitehead+MT%22">Whitehead MT</searchLink>; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA.<br /><searchLink fieldCode="AU" term="%22Turnacioglu+S%22">Turnacioglu S</searchLink>; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA.<br /><searchLink fieldCode="AU" term="%22Pearl+PL%22">Pearl PL</searchLink>; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Gropman+AL%22">Gropman AL</searchLink>; Children's National Medical Center, The George Washington University School of Medicine, Washington, DC, USA AGropman@childrensnational.org.
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  Data: <searchLink fieldCode="JN" term="%228606714%22">Journal of child neurology</searchLink> [J Child Neurol] 2014 Sep; Vol. 29 (9), pp. 1249-56. <i>Date of Electronic Publication: </i>2014 Jul 17.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Sage%22">Sage </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8606714 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1708-8283 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208830738%22">08830738 </searchLink><i>NLM ISO Abbreviation: </i>J Child Neurol <i>Subsets: </i>MEDLINE
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        Value: 10.1177/0883073814538511
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        Text: English
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      – TitleFull: Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
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              Text: 2014 Sep
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