Literature DB >> 35907985

Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation.

Yanping Wei1, Min Qian2, Yingmai Yang2.   

Abstract

Entities:  

Year:  2022        PMID： 35907985     DOI： 10.1007/s10072-022-06305-3

Source DB:  PubMed          Journal:  Neurol Sci        ISSN： 1590-1874            Impact factor:   3.830


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  10 in total

Review 1.  Leigh and Leigh-like syndrome in children and adults.

Authors:  Josef Finsterer
Journal:  Pediatr Neurol       Date:  2008-10       Impact factor: 3.372

2.  Mitochondrial DNA mutations in late-onset Leigh syndrome.

Authors:  Yanping Wei; Liying Cui; Bin Peng
Journal:  J Neurol       Date:  2018-08-20       Impact factor: 4.849

Review 3.  Primary Mitochondrial Disorders of the Pediatric Central Nervous System: Neuroimaging Findings.

Authors:  Fabrício Guimarães Gonçalves; César Augusto Pinheiro Ferreira Alves; Beth Heuer; James Peterson; Angela N Viaene; Sara Reis Teixeira; Juan Sebastián Martín-Saavedra; Savvas Andronikou; Amy Goldstein; Arastoo Vossough
Journal:  Radiographics       Date:  2020 Nov-Dec       Impact factor: 5.333

4.  Clinical and neuroimaging features of the m.10197G>A mtDNA mutation: New case reports and expansion of the phenotype variability.

Authors:  D Tolomeo; A Rubegni; M Severino; F Pochiero; C Bruno; D Cassandrini; A Madeo; S Doccini; M Pedemonte; A Rossi; F D'Amore; M A Donati; M Di Rocco; F M Santorelli; C Nesti
Journal:  J Neurol Sci       Date:  2019-02-06       Impact factor: 3.181

5.  Early spinal cord and brainstem involvement in infantile Leigh syndrome possibly caused by a novel variant.

Authors:  Jeffrey R Tenney; Carlos E Prada; Robert J Hopkin; Barbara E Hallinan
Journal:  J Child Neurol       Date:  2012-11-08       Impact factor: 1.987

6.  Mild clinical manifestation and unusual recovery upon coenzyme Q₁₀ treatment in the first Chinese Leigh syndrome pedigree with mutation m.10197 G>A.

Authors:  Zhiting Chen; Zhenhua Zhao; Qinyong Ye; Ying Chen; Xiaodong Pan; Bin Sun; Huapin Huang; An Zheng
Journal:  Mol Med Rep       Date:  2014-11-10       Impact factor: 2.952

7.  Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia.

Authors:  Kang Wang; Yuji Takahashi; Zong-Liang Gao; Guo-Xiang Wang; Xian-Wen Chen; Jun Goto; Jin-Ning Lou; Shoji Tsuji
Journal:  Neurogenetics       Date:  2009-05-21       Impact factor: 2.660

8.  A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.

Authors:  Jong Hee Chae; Jin Sook Lee; Ki Joong Kim; Yong Seung Hwang; Eduardo Bonilla; Kurenai Tanji; Michio Hirano
Journal:  Pediatr Res       Date:  2007-05       Impact factor: 3.756

9.  The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.

Authors:  Yinglin Leng; Yuhe Liu; Xiaojing Fang; Yao Li; Lei Yu; Yun Yuan; Zhaoxia Wang
Journal:  Mitochondrial DNA       Date:  2014-04-08

10.  Hormone replacement therapy in Leber's hereditary optic neuropathy: Accelerated visual recovery in vivo.

Authors:  Michele Fantini; Samuel Asanad; Rustum Karanjia; Alfredo Sadun
Journal:  J Curr Ophthalmol       Date:  2018-11-03
  10 in total

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