Reply: MELAS can be delineated from CADASIL by genotype and phenotype

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Published inNeurobiology of aging Vol. 99; p. 104
Main Authors Liao, Nai-Yi, Liao, Kwong-Kum, Liao, Yi-Chu, Lee, Yi-Chung
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2021
Subjects
CADASIL - genetics
DNA, Mitochondrial
Genotype
Humans
MELAS Syndrome - genetics
Mutation
Phenotype
Online AccessGet full text

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Author Liao, Nai-Yi
Lee, Yi-Chung
Liao, Yi-Chu
Liao, Kwong-Kum
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  givenname: Kwong-Kum
  surname: Liao
  fullname: Liao, Kwong-Kum
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Cites_doi 10.1111/ene.14183
10.1001/archneur.62.7.1154
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References Apostolova, White, Moore, Davis (bib1) 2005; 62
Liao, Liao, Liao, Lee (bib3) 2020
Castillo, Kwock, Green (bib2) 1995; 1995
Mancuso, Arnold, Bersano, Burlina, Chabriat, Debette, Enzinger, Federico, Filla, Finsterer, Hunt, Lesnik Oberstein, Tournier-Lasserve, Markus (bib4) 2020; 27
32950272 - Neurobiol Aging. 2021 Jan;97:145.e5-145.e6
33840574 - Neurobiol Aging. 2021 Mar 13;:null
Apostolova (10.1016/j.neurobiolaging.2020.10.026_bib1) 2005; 62
Liao (10.1016/j.neurobiolaging.2020.10.026_bib3) 2020
Mancuso (10.1016/j.neurobiolaging.2020.10.026_bib4) 2020; 27
Castillo (10.1016/j.neurobiolaging.2020.10.026_bib2) 1995; 1995
References_xml – volume: 1995
  start-page: 233
  year: 1995
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  ident: bib2
  article-title: MELAS syndrome: imaging and proton MR spectroscopic findings
  publication-title: AJNR. Am. J. Neuroradiol.
  contributor:
    fullname: Green
– volume: 27
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  year: 2020
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  article-title: Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology
  publication-title: Eur. J. Neurol.
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    fullname: Markus
– volume: 62
  start-page: 1154
  year: 2005
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  ident: bib1
  article-title: Deep white matter pathologic features in watershed regions: a novel pattern of central nervous system involvement in MELAS
  publication-title: Arch. Neurol.
  contributor:
    fullname: Davis
– year: 2020
  ident: bib3
  article-title: Mitochondrial DNA m. 3243A> G mutation rarely causes CADASIL-like phenotype
  publication-title: Neurobiol. Aging
  contributor:
    fullname: Lee
– volume: 27
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  article-title: Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology
  publication-title: Eur. J. Neurol.
  doi: 10.1111/ene.14183
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    fullname: Mancuso
– year: 2020
  ident: 10.1016/j.neurobiolaging.2020.10.026_bib3
  article-title: Mitochondrial DNA m. 3243A> G mutation rarely causes CADASIL-like phenotype
  publication-title: Neurobiol. Aging
  contributor:
    fullname: Liao
– volume: 62
  start-page: 1154
  year: 2005
  ident: 10.1016/j.neurobiolaging.2020.10.026_bib1
  article-title: Deep white matter pathologic features in watershed regions: a novel pattern of central nervous system involvement in MELAS
  publication-title: Arch. Neurol.
  doi: 10.1001/archneur.62.7.1154
  contributor:
    fullname: Apostolova
– volume: 1995
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  article-title: MELAS syndrome: imaging and proton MR spectroscopic findings
  publication-title: AJNR. Am. J. Neuroradiol.
  contributor:
    fullname: Castillo
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SubjectTerms CADASIL - genetics
DNA, Mitochondrial
Genotype
Humans
MELAS Syndrome - genetics
Mutation
Phenotype
Title Reply: MELAS can be delineated from CADASIL by genotype and phenotype
URI https://dx.doi.org/10.1016/j.neurobiolaging.2020.10.026
https://www.ncbi.nlm.nih.gov/pubmed/33288335
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Volume 99
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