Literature DB >> 28884978

Response to Letter to the Editor: Can MR spectroscopy and muscle biopsy findings be correlated in MELAS and CPEO?

Feng-Nan Niu1, Hai-Lan Meng2, Ren-Yuan Liu2, Bing Zhang3, Yun Xu2.   

Abstract

Mesh：

Year:  2017        PMID： 28884978      PMCID： PMC6492724          DOI： 10.1111/cns.12752

Source DB:  PubMed          Journal:  CNS Neurosci Ther        ISSN： 1755-5930            Impact factor:   5.243


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  11 in total

Review 1.  Mitochondrial DNA replication and disease: insights from DNA polymerase γ mutations.

Authors:  Jeffrey D Stumpf; William C Copeland
Journal:  Cell Mol Life Sci       Date:  2010-10-08       Impact factor: 9.261

Review 2.  Bigenomic regulation of cytochrome c oxidase in neurons and the tight coupling between neuronal activity and energy metabolism.

Authors:  Margaret T T Wong-Riley
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

Review 3.  Molecular pathology of MELAS and L-arginine effects.

Authors:  Yasutoshi Koga; Nataliya Povalko; Junko Nishioka; Koujyu Katayama; Shuichi Yatsuga; Toyojiro Matsuishi
Journal:  Biochim Biophys Acta       Date:  2011-09-14

4.  Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.

Authors:  S G Pavlakis; P C Phillips; S DiMauro; D C De Vivo; L P Rowland
Journal:  Ann Neurol       Date:  1984-10       Impact factor: 10.422

Review 5.  Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.

Authors:  Mike Gerards; Suzanne C E H Sallevelt; Hubert J M Smeets
Journal:  Mol Genet Metab       Date:  2015-12-19       Impact factor: 4.797

6.  Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox".

Authors:  Ali Naini; Petra Kaufmann; Sara Shanske; Kristin Engelstad; Darryl C De Vivo; Eric A Schon
Journal:  J Neurol Sci       Date:  2004-12-15       Impact factor: 3.181

7.  A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions.

Authors:  Henna Tyynismaa; Emil Ylikallio; Mehul Patel; Maria J Molnar; Ronald G Haller; Anu Suomalainen
Journal:  Am J Hum Genet       Date:  2009-08-06       Impact factor: 11.025

Review 8.  Mitochondrial energy metabolism is regulated via nuclear-coded subunits of cytochrome c oxidase.

Authors:  B Kadenbach; M Hüttemann; S Arnold; I Lee; E Bender
Journal:  Free Radic Biol Med       Date:  2000-08       Impact factor: 7.376

Review 9.  Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome.

Authors:  Douglas M Sproule; Petra Kaufmann
Journal:  Ann N Y Acad Sci       Date:  2008-10       Impact factor: 5.691

10.  Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance.

Authors:  M Cristina Bianchi; Michela Tosetti; Roberta Battini; Maria L Manca; Michelangelo Mancuso; Giovanni Cioni; Raffaello Canapicchi; Gabriele Siciliano
Journal:  AJNR Am J Neuroradiol       Date:  2003 Nov-Dec       Impact factor: 3.825
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