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A rare case of MELAS syndrome caused by mitochondrial DNA m.3256C>T mutation in China.

• Authors : Xiangxin Zheng¹; Man Huang^1,2

• Source: World Journal of Emergency Medicine. Mar2025, Vol. 16 Issue 2, p180-182. 3p.

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Adult-onset mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A case report and review of its conventional and diffusionweighted MRI features.

• Authors : Pui-Hung Ho¹ ; Li, Richard¹; Chi-Yeung Chu²

• Source: Neurology Asia. 2024, Vol. 29 Issue 2, p465-470. 6p.

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From stroke workup to mitochondrial disease: A case report of MELAS

• Authors : Yusuf Sevencan; Siddharth Rode, MD; Ashley Park, MD

Subjects: MELAS syndrome; Mitochondrial disease; Stroke mimic

• Source: Radiology Case Reports, Vol 20, Iss 12, Pp 6248-6252 (2025)

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A Rare Heteroplasmic MT-ND5 Mutation (m.13094T>C) in an Iranian Patient with Adult-Onset MELAS: Diagnostic Challenges and Therapeutic Implications.

• Authors : Amirifard, Hamed¹; Shahbazi, Mojtaba¹; Farahmand, Ghasem¹

• Source: Case Reports in Clinical Practice. Mar/Apr2025, Vol. 10 Issue 2, p83-89. 7p.

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Effective Management of Chronic Intestinal Pseudo-Obstruction in MELAS Using Acotiamide: A Case Report.

• Authors : Kawano, Yuri^1,2,3 (AUTHOR); Taniguchi, Akira^1,4 (AUTHOR); Narita, Yugo^1,4 (AUTHOR)

• Source: Case Reports in Neurology. Sep2024, Vol. 16 Issue 1, p288-293. 6p. 2 Illustrations.

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Arginine Supplementation in MELAS Syndrome: What Do We Know about the Mechanisms?

• Authors : Barros, Camila D. S.¹ (AUTHOR) ; Coutinho, Aryane¹ (AUTHOR); Tengan, Celia H.¹ (AUTHOR)

• Source: International Journal of Molecular Sciences. Apr2024, Vol. 25 Issue 7, p3629. 12p.

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Comprehensive predictors of drug-resistant epilepsy in MELAS: clinical, EEG, imaging, and biochemical factors.

• Authors : Gao R; Department of Neurology, Tianjin Huanhu Hospital, Nankai University, Tianjin, China.; Gu L

Subjects: MELAS Syndrome*/MELAS Syndrome*/MELAS Syndrome*/complications ; MELAS Syndrome*/MELAS Syndrome*/MELAS Syndrome*/physiopathology ; MELAS Syndrome*/MELAS Syndrome*/MELAS Syndrome*/diagnostic imaging

• Source: BMC neurology [BMC Neurol] 2025 Feb 14; Vol. 25 (1), pp. 64. Date of Electronic Publication: 2025 Feb 14.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Mitochondrial gene heterogeneity related to MELAS syndrome: A review of literature.

• Authors : WEN Limin¹; LI Ran¹; HAO Yanlei¹

• Source: Journal of Practical Medicine / Shiyong Yixue Zazhi. 7/10/2024, Vol. 40 Issue 13, p1885-1888. 4p.

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A Rare Heteroplasmic MT-ND5 Mutation (m.13094T>C) in an Iranian Patient with Adult-Onset MELAS: Diagnostic Challenges and Therapeutic Implications

• Authors : Hamed Amirifard; Mojtaba Shahbazi; Ghasem Farahmand

Subjects: MELAS syndrome; MT-ND5 mutation; Heteroplasmy

• Source: Case Reports in Clinical Practice, Vol 10, Iss 2 (2025)

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Dynamic reconfiguration and transition of whole-brain networks in patients with MELAS revealed by a hidden Markov model

• Authors : Qingyun Yu; Rong Wang; Chong Sun

Subjects: MELAS; stroke-like episode; rs-fMRI

• Source: Frontiers in Neurology, Vol 16 (2025)

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