Response to: Letter to the Editor Regarding: The Expanding Phenotype of MELAS Caused by the m.3291 T>C tRNA Mutation E Kelland, C. A. Rupar, Asuri N. Prasad, K. Y. Tay, A. Downie a... by E. Kelland, C.A. Rupar, Asuri N. Prasad, K.Y. Tay, A. Downie, C. Prasad

Subjects: “…MELAS…”
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VERBALINIŲ MELO POŽYMIŲ ATPAŽINIMAS RAŠYTINĖJE IR ŽODINĖJE KOMUNIKACIJOJE by Laima Markevičiūtė, Kristina Vanagaitė

Subjects: “…melas žodžiu…”
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Melas синдром (митохондриална енцефало миопатия, лактатна ацидоза и инсулти) – представяне на клиничен случай... by Teodor Angelov, T. Chamova, S. Cherninkova, A. Elenkova, I. Tournev

Subjects: “…MELAS…”
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Clinical analysis of three children patients with MELAS by Xiao-jun LIU, Yu-qin ZHANG, Yi-jun SONG

Subjects: “…MELAS syndrome…”
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An anesthetic experience with remimazolam for MELAS patients by Atsuhiro Kitaura, Shinichi Nakao

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The expanding phenotype of MELAS caused by the m.3291T>C mutation in the MT-TL1 gene by E. Keilland, C.A. Rupar, Asuri N. Prasad, K.Y. Tay, A. Downie, C. Prasad

Subjects: “…MELAS…”
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Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes by Hueng-Chuen Fan, Hsiu-Fen Lee, Chen-Tang Yue, Ching-Shiang Chi

Subjects: “…MELAS…”
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Case studies of two families with MIDD and MELAS: heteroplasmy level in m.3243A>G mutation and the first report on m.3271T>C mutation in Colombia by Jorge Luis Granadillo De Luque, Manuel Luna, Leonardo Hernández-Reina, Clara Arteaga-Diaz, Juan Manuel Arteaga-Díaz

Subjects: “…MELAS…”
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Mitochondrial encephalomyopathy with lactic acidemia and stroke-like episodes by Xiao-ling YAN, Xue-bin ZHANG, Shu-mei JIN, Fan TANG, Zhu-yu HAN

Subjects: “…MELAS syndrome…”
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Síndrome de Melas: correlación clínica con hallazgos imagenológicos en espectroscopia y tractografía, reporte de caso by Sergio Francisco Ramírez, Jorge Humberto Marín, José Fernando Hernández, Aura Virginia González, Orlando López, Adriana Lucía Posso, Luis Fernando Roa, Juan Diego Vargas, Gabriel Augusto Castillo, Juan Andrés Monsalve

Subjects: “…Melas…”
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Targeted elimination of mutant mitochondrial DNA in MELAS-iPSCs by mitoTALENs by Yi Yang, Han Wu, Xiangjin Kang, Yanhui Liang, Ting Lan, Tianjie Li, Tao Tan, Jiangyun Peng, Quanjun Zhang, Geng An, Yali Liu, Qian Yu, Zhenglai Ma, Ying Lian, Boon Seng Soh, Qingfeng Chen, Ping Liu, Yaoyong Chen, Xiaofang Sun, Rong Li, Xiumei Zhen, Ping Liu, Yang Yu, Xiaoping Li, Yong Fan

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Vitelliform maculopathy in MELAS syndrome by Cody Jahrig, Cristy A. Ku, Molly Marra, Mark E. Pennesi, Paul Yang

Subjects: “…MELAS…”
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Arrhythmia as a cardiac manifestation in MELAS syndrome by Tamara Thomas, William J. Craigen, Ryan Moore, Richard Czosek, John L. Jefferies

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Síndrome de Melas: correlación clínica con hallazgos imagenológicos en espectroscopia y tractografía, reporte de caso by Sergio Francisco Ramírez, Jorge Humberto Marín, José Fernando Hernández, Aura Virginia González, Orlando López, Adriana Lucía Posso, Luis Fernando Roa, Juan Diego Vargas, Gabriel Augusto Castillo, Juan Andrés Monsalve

Subjects: “…Melas…”
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Refractory Hypotension in a Late-Onset Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Male with m.3243 A>G Mutation: A Case Report by Youjie Wang, Enhui Zhang, Chen Ye, Bo Wu

Subjects: “…MELAS…”
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Identificación de mutaciones en pacientes diagnosticados con MELAS y/o MERRF by Andrés Ruiz, Gabriel Bedoya Berrío, José William Cornejo Ochoa, Victoria Parra, Luis Carlos Burgos Herrera

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Case report: A double pathogenic mutation in a patient with late-onset MELAS/PEO overlap syndrome by Qiu Yan Zhao, Wen Zhao Zhang, Xue Lian Zhu, Fei Qiao, Li Yuan Jia, Bi Li, Yong Xiao, Han Chen, Yu Zhang, Yun Guo Chen, Yong Liang Wang

Subjects: “…MELAS…”
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The characteristics of cardiac involvement in 113 patients with mitochondrial encephalomyopathy with lactic academia and stroke⁃like episodes by ZHAO Xu⁃tong, WANG Jie, ZHUO Yong⁃jie, WANG Qi, YANG Ying, LIU Lin, DING Wen⁃hui, YUAN Yun, WANG Zhao⁃xia

Subjects: “…melas syndrome…”
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A rare cause of mixed hypertrophic and dilated phenotype cardiomyopathy – the MELAS syndrome by Casian Mihnea, Dragotoiu Nic, Onciul Sebastian, Popescu Bogdan A., Jurcuţ Ruxandra

Subjects: “…melas…”
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A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene by Tao-Ran Li, Tao-Ran Li, Qun Wang, Mao-Mao Liu, Rui-Juan Lv

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