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Results for
""MELAS Syndrome""[mesh_terms]

36 Results

Searching titles within these results

The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.

Jennifer L Northrop, Fernando Scaglia

CNS drugs 2006;20(6):443-64

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Abstract

A novel tRNASer(AGY) 12244G > a variant impairs mitochondrial function and presents with classical MELAS phenotype.

Xingyu Zhuang, Jiayin Wang, Jianing Wang, Yan Lin, Chuanzhu Yan, Kunqian Ji

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2026;47(3):264

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Abstract

Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome.

Young-Mock Lee, Ji-Hoon Na

Biomolecules 2025;14(12):

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Abstract

THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS.

Katie Nahay Robinson, Sari Terrazas, Samantha Giordano-Mooga, Neena A Xavier

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020;26(2):241-246

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Abstract

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

Celia H Tengan, Camila D S Barros, Aryane Coutinho

International journal of molecular sciences 2024;25(7):

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Abstract

Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements.

Michelangelo Mancuso, Marcello Bellusci, Valerio Carelli, Irenaeus de Coo, Daria Diodato, Felix Distelmaier, Omar Hikmat, Michio Hirano, Rita Horvath, Amel Karaa, Thomas Klopstock, Mary Kay Koenig, Cornelia Kornblum, Chiara La Morgia, Piervito Lopriore, Mika Henrik Martikainen, Robert McFarland, Olimpia Musumeci, Robert D S Pitceathly, Guido Primiano, Shamima Rahman, Fernando Scaglia, Andrew Schaefer, Manuel Schiff, Luisa Semmler, Costanza Lamperti, Serenella Servidei

European journal of neurology 2026;33(4):e70588

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Abstract

Assessment of Nitric Oxide Production in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome with the Use of a Stable Isotope Tracer Infusion Technique.

Ayman W El-Hattab, Farook Jahoor

The Journal of nutrition 2017;147(7):1251-1257

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Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications.

Razek Georges Coussa, Sumit Parikh, Elias I Traboulsi

Survey of ophthalmology 2022;66(5):838-855

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Abstract

Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.

Kristin M Santa

Pharmacotherapy 2011;30(11):1179-96

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MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions: A Case Report and Literature Review.

Zhaoxia Wang, Yanping Zhu, Wenxia Wang, Jing Shi, Xuan Chen, Qing Liu, Chao Wen, Xiaolian Xing, Yangli Su

The neurologist 2025;30(2):75-79

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Abstract

Mitochondrial metabolic stroke: Phenotype and genetics of stroke-like episodes.

Josef Finsterer

Journal of the neurological sciences 2020;400():135-141

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Abstract

Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.

Magdalena Hoptasz, Adam Szczuciński, Jacek Losy

Neurologia i neurochirurgia polska 2014;48(2):150-3

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Abstract

High-dose oral glutamine supplementation reduces elevated glutamate levels in cerebrospinal fluid in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.

Montserrat Morales-Conejo, Aitor Delmiro, María Morán, Cristina Domínguez-González, Elena Arranz-Canales, Ana Ramos-González, Joaquín Arenas, Miguel A Martín, Jesús González de la Aleja, María Paz Guerrero-Molina

European journal of neurology 2023;30(2):538-547

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Abstract

Clinical manifestation of mitochondrial diseases.

Martin Magner, Hana Kolářová, Tomáš Honzik, Ivana Švandová, Jiří Zeman

Developmental period medicine 2016;19(4):441-9

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Abstract

Stroke-like episodes, peri-episodic seizures, and MELAS mutations.

Josef Finsterer, Salma Majid Wakil

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2016;20(6):824-829

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Results: 1 – 15 / 36

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Results for ""MELAS Syndrome""[mesh_terms]

The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.

A novel tRNASer(AGY) 12244G > a variant impairs mitochondrial function and presents with classical MELAS phenotype.

Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome.

THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS.

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

Diagnostic Criteria and Management of MELAS and Stroke-Like Episodes: Consensus-Based Statements.

Assessment of Nitric Oxide Production in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome with the Use of a Stable Isotope Tracer Infusion Technique.

Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications.

Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.

MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions: A Case Report and Literature Review.

Mitochondrial metabolic stroke: Phenotype and genetics of stroke-like episodes.

Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report.

High-dose oral glutamine supplementation reduces elevated glutamate levels in cerebrospinal fluid in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.

Clinical manifestation of mitochondrial diseases.

Stroke-like episodes, peri-episodic seizures, and MELAS mutations.

Results for
""MELAS Syndrome""[mesh_terms]