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Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.
Ophthalmic Genet. 2016 Jun;37(2):217-27. doi: 10.3109/13816810.2015.1028647. Epub 2015 Sep 2.
Ophthalmic Genet. 2016.
PMID: 26331342
Prevalence of retinal hemorrhages in pediatric patients after in-hospital cardiopulmonary resuscitation: a prospective study.
Odom A, Christ E, Kerr N, Byrd K, Cochran J, Barr F, Bugnitz M, Ring JC, Storgion S, Walling R, Stidham G, Quasney MW.
Odom A, et al.
Pediatrics. 1997 Jun;99(6):E3. doi: 10.1542/peds.99.6.e3.
Pediatrics. 1997.
PMID: 9164799
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