Literature DB >> 30924003

Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype.

Josef Finsterer1, Sinda Zarrouk-Mahjoub2.   

Abstract

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Year:  2019        PMID： 30924003     DOI： 10.1007/s10633-019-09690-x

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN： 0012-4486            Impact factor:   2.379


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  4 in total

Review 1.  Mitochondrial vasculopathy.

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

2.  Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome.

Authors:  Kenji Ozawa; Kiyofumi Mochizuki; Yusuke Manabe; Nobuaki Yoshikura; Takayoshi Shimohata; Ichizo Nishino; Yu-Ichi Goto
Journal:  Doc Ophthalmol       Date:  2019-01-30       Impact factor: 2.379

Review 3.  Management of mitochondrial stroke-like-episodes.

Authors:  J Finsterer
Journal:  Eur J Neurol       Date:  2009-09-23       Impact factor: 6.089

4.  Clinical characteristics of patients with non-specific and non-categorized mitochondrial diseases.

Authors:  Jeong Tae Kim; Yun Jin Lee; Young Mock Lee; Hoon Chul Kang; Joon Soo Lee; Heung Dong Kim
Journal:  Acta Paediatr       Date:  2009-07-31       Impact factor: 2.299
  4 in total

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