Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome: a case report-Reference-Cited by-同舟云学术

Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome: a case report

Published:2023-03-05 Issue:3 Volume:47 Page:227-235
ISSN:0191-3123
Container-title:Ultrastructural Pathology
language:en
Short-container-title:Ultrastructural Pathology

Author:

Ru Yong-Xin¹,Ying Li²,Dong Shu-Xu¹,Yi Hui-Ming¹,Jing Liu¹,Yongqiang Zhang²

Affiliation:

1. State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Haihe Laboratory of Cell Ecosystem, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, BJ, China

2. Tianjin Neurological Institute, Tianjin Medical University General Hospital, TJ, China

Funder

funding

Publisher

Informa UK Limited

Subject

Structural Biology,Pathology and Forensic Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/01913123.2023.2184892

Reference18 articles.

1. Mitochondrial disorders: aetiologies, models systems, and candidate therapies

2. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options

3. The broadening spectrum of mitochondrial disease: Shifts in the diagnostic paradigm

4. Chronic progressive external ophthalmoplegia: A correlative study of mitochondrial DNA deletions and their phenotypic expression in muscle biopsies

5. A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

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