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Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
Werner KG, Morel CF, Kirton A, Benseler SM, Shoffner JM, Addis JB, Robinson BH, Burrowes DM, Blaser SI, Epstein LG, Feigenbaum AS. Werner KG, et al. Among authors: burrowes dm. Pediatr Neurol. 2009 Jul;41(1):27-33. doi: 10.1016/j.pediatrneurol.2009.02.010. Pediatr Neurol. 2009. PMID: 19520270
Neuroimaging findings in children with rare or novel de novo chromosomal anomalies.
Epstein LG, Jalali A, Chary AN, Khan S, Ross J, Coppinger J, Carlson K, Charrow J, Burton B, Zimmerman D, Curran J, Kim F, Nguyen P, Burrowes D, Angle B, Stack C, Shaffer L, Kessler JA, Bassuk AG. Epstein LG, et al. Birth Defects Res A Clin Mol Teratol. 2008 Apr;82(4):200-10. doi: 10.1002/bdra.20443. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18302267
Intracranial vascular abnormalities in patients with Alagille syndrome.
Emerick KM, Krantz ID, Kamath BM, Darling C, Burrowes DM, Spinner NB, Whitington PF, Piccoli DA. Emerick KM, et al. Among authors: burrowes dm. J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):99-107. doi: 10.1097/01.mpg.0000162776.67758.2f. J Pediatr Gastroenterol Nutr. 2005. PMID: 15990638
24 results