Literature DB >> 26823911

Genetic background and phenotypic heterogeneity of MELAS and maternally inherited diabetes and deafness.

Josef Finsterer1, Marlies Frank2, Anushree Mishra3.   

Abstract

Entities:  

Keywords:  Non-compaction; acquired; chromosomal; left ventricular hypertrabeculation; mitochondrial

Mesh：

Substances：

Year:  2015        PMID： 26823911      PMCID： PMC4713697     

Source DB:  PubMed          Journal:  Int J Clin Exp Pathol        ISSN： 1936-2625


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  4 in total

1.  A case of cluster headache associated with mitochondrial DNA deletions.

Authors:  P Montagna; P Cortelli; B Barbiroli
Journal:  Muscle Nerve       Date:  1998-01       Impact factor: 3.217

2.  Manifestations of the mitochondrial A3243G mutation.

Authors:  Josef Finsterer
Journal:  Int J Cardiol       Date:  2008-07-26       Impact factor: 4.164

3.  Maternally inherited diabetes and deafness (MIDD): diagnosis and management.

Authors:  Aye Naing; Manohar Kenchaiah; Binu Krishnan; Farheen Mir; Amanda Charnley; Catherine Egan; Gul Bano
Journal:  J Diabetes Complications       Date:  2014-03-12       Impact factor: 2.852

4.  Mitochondrial genetic analysis in a Chinese family suffering from both mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes and diabetes.

Authors:  Weiwei Li; Wei Zhang; Fang Li; Cailing Wang
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01
  4 in total

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