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Stroke, ISSN 0039-2499, 07/2016, Volume 47, Issue 7, pp. 1702 - 1709
Journal Article
Kidney International, ISSN 0085-2538, 03/2015, Volume 87, Issue 3, pp. 610 - 622
Journal Article
The American Journal of Forensic Medicine and Pathology, ISSN 0195-7910, 06/2016, Volume 37, Issue 2, pp. 54 - 56
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 5/2016, Volume 39, Issue 3, pp. 465 - 466
Auditory impairment in mitochondrial disorders are usually due to peripheral sensorineural dysfunction. Central deafness is only rarely reported. We report... 
Human Genetics | Biochemistry, general | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | MELAS Syndrome - complications | Humans | Hearing Loss, Central - etiology | Stroke - complications | Male | Child | Deafness - etiology | Stroke (Disease) | Deafness | Sleep | Hospitals | Index Medicus | Images in Metabolic Medicine
Journal Article
The Neurologist, ISSN 1074-7931, 05/2019, Volume 24, Issue 3, pp. 90 - 92
Journal Article
Neurology, ISSN 0028-3878, 07/2015, Volume 85, Issue 2, pp. 197 - 198
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome (MT-TL1 gene) is a progressive neurologic disorder with stroke-like... 
CLINICAL NEUROLOGY | MELAS Syndrome - complications | Stroke - etiology | Humans | MELAS Syndrome - drug therapy | Male | Stroke - drug therapy | Arginine - therapeutic use | Child | Index Medicus | Abridged Index Medicus | Clinical | 157 | Scientific Notes | 227 | 120
Journal Article