Kerr NC - Search Results

1

Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.

Wilkin J, Kerr NC, Byrd KW, Ward JC, Iannaccone A. Wilkin J, et al. Among authors: kerr nc. Ophthalmic Genet. 2016 Jun;37(2):217-27. doi: 10.3109/13816810.2015.1028647. Epub 2015 Sep 2. Ophthalmic Genet. 2016. PMID: 26331342

2

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

3

Visual evoked potentials in children with neurofibromatosis type 1.

Iannaccone A, McCluney RA, Brewer VR, Spiegel PH, Taylor JS, Kerr NC, Pivnick EK. Iannaccone A, et al. Among authors: kerr nc. Doc Ophthalmol. 2002 Jul;105(1):63-81. doi: 10.1023/a:1015719803719. Doc Ophthalmol. 2002. PMID: 12152804

4

Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.

Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM. Iannaccone A, et al. Among authors: kerr nc. Arch Ophthalmol. 2011 Feb;129(2):211-7. doi: 10.1001/archophthalmol.2010.367. Arch Ophthalmol. 2011. PMID: 21320969

5

Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene.

Cox KF, Kerr NC, Kedrov M, Nishimura D, Jennings BJ, Stone EM, Sheffield VC, Iannaccone A. Cox KF, et al. Among authors: kerr nc. Vision Res. 2012 Dec 15;75:77-87. doi: 10.1016/j.visres.2012.08.005. Epub 2012 Aug 24. Vision Res. 2012. PMID: 22940089 Free article.

6

Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene.

Hood MP, Kerr NC, Smaoui N, Iannaccone A. Hood MP, et al. Among authors: kerr nc. Doc Ophthalmol. 2015 Apr;130(2):157-64. doi: 10.1007/s10633-014-9477-3. Epub 2015 Jan 3. Doc Ophthalmol. 2015. PMID: 25555363

7

Type 3 Pfeiffer syndrome with normal thumbs.

Kerr NC, Wilroy RS Jr, Kaufman RA. Kerr NC, et al. Am J Med Genet. 1996 Dec 11;66(2):138-43. doi: 10.1002/(SICI)1096-8628(19961211)66:2<138::AID-AJMG3>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8958319

8

Reversal of optic canal stenosis in osteopetrosis after bone marrow transplant.

Kerr NC, Wang WC, Mohadjer Y, Haik BG, Kaste SC, Horwitz EM. Kerr NC, et al. Am J Ophthalmol. 2000 Sep;130(3):370-2. doi: 10.1016/s0002-9394(00)00543-2. Am J Ophthalmol. 2000. PMID: 11020426

9

Persistent binocular diplopia in childhood following successful treatment for esotropia: a case series.

Tae T, Devould C, Skilbeck L, Hoehn ME, Kerr N. Tae T, et al. Am Orthopt J. 2014;64:117-22. doi: 10.3368/aoj.64.1.117. Am Orthopt J. 2014. PMID: 25313121

10

Traumatic hyphemas in children secondary to corporal punishment with a belt.

Calzada JI, Kerr NC. Calzada JI, et al. Among authors: kerr nc. Am J Ophthalmol. 2003 May;135(5):719-20. doi: 10.1016/s0002-9394(02)01890-1. Am J Ophthalmol. 2003. PMID: 12719088

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