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- Mutational Analysis of Whole Mitochondrial DNA in Patients with MELAS and MERRF Diseases
- Acute Renal Failure and the MELAS Syndrome, a Mitochondrial Encephalomyopathy1 Fred Hsieh, Reginald Gohh, and Lance Dworkin2
- Investigation of Muscle Disease
- Anaesthesia in Children with Neuromuscular Disease
- Mitochondrial Disorders: Analysis of Their Clinical and Imaging Characteristics
- Evaluation and Treatment of Myopathies
- Mitochondrial Disease and Anesthesia ª the Author(S) 2017 DOI: 10.1177/2326409817707770 Journals.Sagepub.Com/Home/Iem
- Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
- Diagnosis and Management of Mitochondrial Disease: a Consensus Statement from the Mitochondrial Medicine Society
- Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like
- Inherited Neuromuscular Disorders: Which Role Forserum Biomarkers?
- Movement Disorders with Neuronal Antibodies: Syndromic Approach, Genetic Parallels and Pathophysiology
- MELAS Syndrome), Is a Rare Disorder That Affects Many of the Body’S Systems, Particularly the Brain and Nervous System (Encephalo-) and Muscles (Myopathy)
- MELAS Syndrome: an Update Mingzheng Aaron Goh* and Shiva Dindyal Department of Surgery, Basildon and Thurrock University Hospitals NHS Foundation Trust, UK
- MELAS Syndrome): Diagnostic Criteria, Features of Epileptic Seizures and Treatment Approaches
- Chronic Anemia As a Manifestation of MELAS Syndrome
- Type 1 Established Condition List
- Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies