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"I just want to be treated like a normal person": Oral health care experiences of transgender adolescents and young adults.

Macdonald DW, Grossoehme DH, Mazzola A, Pestian T, Schwartz SB.

J Am Dent Assoc. 2019 Jun 19. pii: S0002-8177(19)30260-0. doi: 10.1016/j.adaj.2019.03.025. [Epub ahead of print]


Triplex real-time PCR assay for the detection of Streptococcus pneumoniae, Neisseria meningitidis and Haemophilus influenzae directly from clinical specimens without extraction of DNA.

Ouattara M, Whaley MJ, Jenkins LT, Schwartz SB, Traoré RO, Diarra S, Collard JM, Sacchi CT, Wang X.

Diagn Microbiol Infect Dis. 2019 Mar;93(3):188-190. doi: 10.1016/j.diagmicrobio.2018.10.008. Epub 2018 Oct 16.


CIED Cybersecurity Risks in an Increasingly Connected World.

Paulsen JE, Hazelett MB, Schwartz SB.

Circulation. 2018 Sep 18;138(12):1181-1183. doi: 10.1161/CIRCULATIONAHA.118.035021. No abstract available.


Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A.

Hum Mol Genet. 2019 Jan 1;28(1):175. doi: 10.1093/hmg/ddy342. No abstract available.


Sexual orientation-related oral health disparities in the United States.

Schwartz SB, Sanders AE, Lee JY, Divaris K.

J Public Health Dent. 2019 Dec;79(1):18-24. doi: 10.1111/jphd.12290. Epub 2018 Oct 2.


A qualitative exploration: questioning multisource feedback in residency education.

Yama BA, Hodgins M, Boydell K, Schwartz SB.

BMC Med Educ. 2018 Jul 24;18(1):170. doi: 10.1186/s12909-018-1270-7.


Pediatric Dentists' Attitudes, Perceptions, and Experience with the Affordable Care Act.

Schwartz SB, Lee JY, Casamassimo PS, Reggiardo P, Wright R, Litch CS.

Pediatr Dent. 2017 Sep 15;39(5):392-396.


Nontuberculous Mycobacterium Infections Associated With Heater-Cooler Devices.

Allen KB, Yuh DD, Schwartz SB, Lange RA, Hopkins R, Bauer K, Marders JA, Delgado Donayre J, Milligan N, Wentz C.

Ann Thorac Surg. 2017 Oct;104(4):1237-1242. doi: 10.1016/j.athoracsur.2017.04.067. Epub 2017 Aug 16.


Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 Gene.

Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choi W, Sheplock R, Swider M, Kosyk MS, Schwartz SB, Stone EM, Fishman GA.

Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2609-2622. doi: 10.1167/iovs.17-21560.


Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene.

Aguirre GK, Butt OH, Datta R, Roman AJ, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG.

Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):959-973. doi: 10.1167/iovs.16-20413.


L.G.B.T: Let's Go Beyond Teeth.

Schwartz SB.

Pediatr Dent. 2017 Mar 15;39(2):90-92. No abstract available.


Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D Mutations.

Jacobson SG, Cideciyan AV, Sumaroka A, Roman AJ, Charng J, Lu M, Choudhury S, Schwartz SB, Heon E, Fishman GA, Boye SE.

Am J Ophthalmol. 2017 May;177:44-57. doi: 10.1016/j.ajo.2017.02.003. Epub 2017 Feb 16.


Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Charng J, Cideciyan AV, Jacobson SG, Sumaroka A, Schwartz SB, Swider M, Roman AJ, Sheplock R, Anand M, Peden MC, Khanna H, Heon E, Wright AF, Swaroop A.

Hum Mol Genet. 2016 Dec 15;25(24):5444-5459. doi: 10.1093/hmg/ddw361. Erratum in: Hum Mol Genet. 2019 Jan 1;28(1):175.


Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin Mutations.

Jacobson SG, McGuigan DB 3rd, Sumaroka A, Roman AJ, Gruzensky ML, Sheplock R, Palma J, Schwartz SB, Aleman TS, Cideciyan AV.

Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4847-4858. doi: 10.1167/iovs.16-19890.


Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations.

Sumaroka A, Matsui R, Cideciyan AV, McGuigan DB 3rd, Sheplock R, Schwartz SB, Jacobson SG.

Invest Ophthalmol Vis Sci. 2016 Jul 1;57(9):OCT253-61. doi: 10.1167/iovs.15-18860.


Isospin Mixing Reveals ^{30}P(p,γ)^{31}S Resonance Influencing Nova Nucleosynthesis.

Bennett MB, Wrede C, Brown BA, Liddick SN, Pérez-Loureiro D, Bardayan DW, Chen AA, Chipps KA, Fry C, Glassman BE, Langer C, Larson NR, McNeice EI, Meisel Z, Ong W, O'Malley PD, Pain SD, Prokop CJ, Schatz H, Schwartz SB, Suchyta S, Thompson P, Walters M, Xu X.

Phys Rev Lett. 2016 Mar 11;116(10):102502. doi: 10.1103/PhysRevLett.116.102502. Epub 2016 Mar 8.


SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.

Matsui R, McGuigan Iii DB, Gruzensky ML, Aleman TS, Schwartz SB, Sumaroka A, Koenekoop RK, Cideciyan AV, Jacobson SG.

Ophthalmic Genet. 2016 Sep;37(3):333-8. doi: 10.3109/13816810.2015.1130154. Epub 2016 Feb 8.


Leber Congenital Amaurosis: Genotypes and Retinal Structure Phenotypes.

Jacobson SG, Cideciyan AV, Huang WC, Sumaroka A, Nam HJ, Sheplock R, Schwartz SB.

Adv Exp Med Biol. 2016;854:169-75. doi: 10.1007/978-3-319-17121-0_23.


Molecular Heterogeneity Within the Clinical Diagnosis of Pericentral Retinal Degeneration.

Matsui R, Cideciyan AV, Schwartz SB, Sumaroka A, Roman AJ, Swider M, Huang WC, Sheplock R, Jacobson SG.

Invest Ophthalmol Vis Sci. 2015 Sep;56(10):6007-18. doi: 10.1167/iovs.15-17174.


Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease Front.

Cideciyan AV, Swider M, Schwartz SB, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2015 Sep;56(10):5946-55. doi: 10.1167/iovs.15-17698.


Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast.

Roman AJ, Cideciyan AV, Matsui R, Sheplock R, Schwartz SB, Jacobson SG.

BMC Ophthalmol. 2015 Aug 8;15:98. doi: 10.1186/s12886-015-0085-0.


Improvement and decline in vision with gene therapy in childhood blindness.

Jacobson SG, Cideciyan AV, Roman AJ, Sumaroka A, Schwartz SB, Heon E, Hauswirth WW.

N Engl J Med. 2015 May 14;372(20):1920-6. doi: 10.1056/NEJMoa1412965. Epub 2015 May 3.


Blue cone monochromacy: visual function and efficacy outcome measures for clinical trials.

Luo X, Cideciyan AV, Iannaccone A, Roman AJ, Ditta LC, Jennings BJ, Yatsenko SA, Sheplock R, Sumaroka A, Swider M, Schwartz SB, Wissinger B, Kohl S, Jacobson SG.

PLoS One. 2015 Apr 24;10(4):e0125700. doi: 10.1371/journal.pone.0125700. eCollection 2015.


Protein misfolding and the pathogenesis of ABCA4-associated retinal degenerations.

Zhang N, Tsybovsky Y, Kolesnikov AV, Rozanowska M, Swider M, Schwartz SB, Stone EM, Palczewska G, Maeda A, Kefalov VJ, Jacobson SG, Cideciyan AV, Palczewski K.

Hum Mol Genet. 2015 Jun 1;24(11):3220-37. doi: 10.1093/hmg/ddv073. Epub 2015 Feb 24.


Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy.

Zelinger L, Cideciyan AV, Kohl S, Schwartz SB, Rosenmann A, Eli D, Sumaroka A, Roman AJ, Luo X, Brown C, Rosin B, Blumenfeld A, Wissinger B, Jacobson SG, Banin E, Sharon D.

Ophthalmology. 2015 May;122(5):997-1007. doi: 10.1016/j.ophtha.2014.11.025. Epub 2015 Jan 21.


Pseudo-fovea formation after gene therapy for RPE65-LCA.

Cideciyan AV, Aguirre GK, Jacobson SG, Butt OH, Schwartz SB, Swider M, Roman AJ, Sadigh S, Hauswirth WW.

Invest Ophthalmol Vis Sci. 2014 Dec 23;56(1):526-37. doi: 10.1167/iovs.14-15895.


Advancing regulatory science to bring novel medical devices for use in emergency care to market: the role of the Food and Drug Administration.

Scully CG, Forrest S, Galeotti L, Schwartz SB, Strauss DG.

Ann Emerg Med. 2015 Apr;65(4):400-3. doi: 10.1016/j.annemergmed.2014.07.008. Epub 2014 Aug 13. Review.


TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.

Jacobson SG, Cideciyan AV, Huang WC, Sumaroka A, Roman AJ, Schwartz SB, Luo X, Sheplock R, Dauber JM, Swider M, Stone EM.

Invest Ophthalmol Vis Sci. 2014 Jul 29;55(8):5354-64. doi: 10.1167/iovs.14-14570.


Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.

Huang WC, Cideciyan AV, Roman AJ, Sumaroka A, Sheplock R, Schwartz SB, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2014 Mar 20;55(3):1810-22. doi: 10.1167/iovs.13-13768.


Classical-NOVA CONTRIBUTION to the Milky Way's ²⁶Al abundance: exit channel of the key ²⁵Al(p,γ) ²⁶Si resonance.

Bennett MB, Wrede C, Chipps KA, José J, Liddick SN, Santia M, Bowe A, Chen AA, Cooper N, Irvine D, McNeice E, Montes F, Naqvi F, Ortez R, Pain SD, Pereira J, Prokop C, Quaglia J, Quinn SJ, Schwartz SB, Shanab S, Simon A, Spyrou A, Thiagalingam E.

Phys Rev Lett. 2013 Dec 6;111(23):232503. Epub 2013 Dec 4.


Intravenous acetaminophen: an alternative to opioids for pain management?

Schwartz SB, Rauch D.

Hosp Pediatr. 2013 Jul;3(3):294-6. No abstract available.


Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy.

Cideciyan AV, Hufnagel RB, Carroll J, Sumaroka A, Luo X, Schwartz SB, Dubra A, Land M, Michaelides M, Gardner JC, Hardcastle AJ, Moore AT, Sisk RA, Ahmed ZM, Kohl S, Wissinger B, Jacobson SG.

Hum Gene Ther. 2013 Dec;24(12):993-1006. doi: 10.1089/hum.2013.153. Epub 2013 Oct 30.


Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement.

Cideciyan AV, Jacobson SG, Beltran WA, Sumaroka A, Swider M, Iwabe S, Roman AJ, Olivares MB, Schwartz SB, Komáromy AM, Hauswirth WW, Aguirre GD.

Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):E517-25. doi: 10.1073/pnas.1218933110. Epub 2013 Jan 22.


Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutations.

Roman AJ, Cideciyan AV, Schwartz SB, Olivares MB, Heon E, Jacobson SG.

Invest Ophthalmol Vis Sci. 2013 Feb 15;54(2):1378-83. doi: 10.1167/iovs.12-11341.


Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.

Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, Zanlonghi X, Lancelot ME, Michiels C, Schwartz SB, Bocquet B; Congenital Stationary Night Blindness Consortium, Antonio A, Audier C, Letexier M, Saraiva JP, Luu TD, Sennlaub F, Nguyen H, Poch O, Dollfus H, Lecompte O, Kohl S, Sahel JA, Bhattacharya SS, Audo I.

Am J Hum Genet. 2013 Jan 10;92(1):67-75. doi: 10.1016/j.ajhg.2012.10.023. Epub 2012 Dec 13.


Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease.

Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, Bennett J, Sieving PA, Andreasson S, Duncan JL, Fishman GA, Iannaccone A, Weleber RG, Jacobson SG, Heckenlively JR, Swaroop A.

Invest Ophthalmol Vis Sci. 2012 Dec 13;53(13):8232-7. doi: 10.1167/iovs.12-11025.


Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants.

Jacobson SG, Cideciyan AV, Peshenko IV, Sumaroka A, Olshevskaya EV, Cao L, Schwartz SB, Roman AJ, Olivares MB, Sadigh S, Yau KW, Heon E, Stone EM, Dizhoor AM.

Hum Mol Genet. 2013 Jan 1;22(1):168-83. doi: 10.1093/hmg/dds421. Epub 2012 Oct 3.


RPGR-associated retinal degeneration in human X-linked RP and a murine model.

Huang WC, Wright AF, Roman AJ, Cideciyan AV, Manson FD, Gewaily DY, Schwartz SB, Sadigh S, Limberis MP, Bell P, Wilson JM, Swaroop A, Jacobson SG.

Invest Ophthalmol Vis Sci. 2012 Aug 15;53(9):5594-608. doi: 10.1167/iovs.12-10070.


Macular function in macular degenerations: repeatability of microperimetry as a potential outcome measure for ABCA4-associated retinopathy trials.

Cideciyan AV, Swider M, Aleman TS, Feuer WJ, Schwartz SB, Russell RC, Steinberg JD, Stone EM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2012 Feb 21;53(2):841-52. doi: 10.1167/iovs.11-8415. Print 2012 Feb.


Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of concept.

Dinculescu A, Estreicher J, Zenteno JC, Aleman TS, Schwartz SB, Huang WC, Roman AJ, Sumaroka A, Li Q, Deng WT, Min SH, Chiodo VA, Neeley A, Liu X, Shu X, Matias-Florentino M, Buentello-Volante B, Boye SL, Cideciyan AV, Hauswirth WW, Jacobson SG.

Hum Gene Ther. 2012 Apr;23(4):367-76. doi: 10.1089/hum.2011.169. Epub 2012 Jan 26.


Autosomal recessive retinitis pigmentosa caused by mutations in the MAK gene.

Stone EM, Luo X, Héon E, Lam BL, Weleber RG, Halder JA, Affatigato LM, Goldberg JB, Sumaroka A, Schwartz SB, Cideciyan AV, Jacobson SG.

Invest Ophthalmol Vis Sci. 2011 Dec 28;52(13):9665-73. doi: 10.1167/iovs.11-8527.


Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.

Jacobson SG, Cideciyan AV, Ratnakaram R, Heon E, Schwartz SB, Roman AJ, Peden MC, Aleman TS, Boye SL, Sumaroka A, Conlon TJ, Calcedo R, Pang JJ, Erger KE, Olivares MB, Mullins CL, Swider M, Kaushal S, Feuer WJ, Iannaccone A, Fishman GA, Stone EM, Byrne BJ, Hauswirth WW.

Arch Ophthalmol. 2012 Jan;130(1):9-24. doi: 10.1001/archophthalmol.2011.298. Epub 2011 Sep 12.


Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, Schwartz SB, Olivares MB, Russell RC, Steinberg JD, Kenna MA, Kimberling WJ, Rehm HL, Williams DS.

Invest Ophthalmol Vis Sci. 2011 Oct 7;52(11):7924-36. doi: 10.1167/iovs.11-8313.


Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.

Aleman TS, Cideciyan AV, Aguirre GK, Huang WC, Mullins CL, Roman AJ, Sumaroka A, Olivares MB, Tsai FF, Schwartz SB, Vandenberghe LH, Limberis MP, Stone EM, Bell P, Wilson JM, Jacobson SG.

Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6898-910. doi: 10.1167/iovs.11-7701.


Infectious aortitis: a rare cause of chest pain in a child.

Schwartz SB, Fisher D, Reinus C, Shahroor S.

Pediatr Emerg Care. 2011 Jul;27(7):654-6. doi: 10.1097/PEC.0b013e318222561f.


Impact of diabetes on burn injury: preliminary results from prospective study.

Schwartz SB, Rothrock M, Barron-Vaya Y, Bendell C, Kamat A, Midgett M, Abshire J, Biebighauser K, Staiano-Coico LF, Yurt RW.

J Burn Care Res. 2011 May-Jun;32(3):435-41. doi: 10.1097/BCR.0b013e318217f954.


A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews.

Zelinger L, Banin E, Obolensky A, Mizrahi-Meissonnier L, Beryozkin A, Bandah-Rozenfeld D, Frenkel S, Ben-Yosef T, Merin S, Schwartz SB, Cideciyan AV, Jacobson SG, Sharon D.

Am J Hum Genet. 2011 Feb 11;88(2):207-15. doi: 10.1016/j.ajhg.2011.01.002. Epub 2011 Feb 3.


Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy.

Cideciyan AV, Rachel RA, Aleman TS, Swider M, Schwartz SB, Sumaroka A, Roman AJ, Stone EM, Jacobson SG, Swaroop A.

Hum Mol Genet. 2011 Apr 1;20(7):1411-23. doi: 10.1093/hmg/ddr022. Epub 2011 Jan 18.


Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome.

Stone EM, Cideciyan AV, Aleman TS, Scheetz TE, Sumaroka A, Ehlinger MA, Schwartz SB, Fishman GA, Traboulsi EI, Lam BL, Fulton AB, Mullins RF, Sheffield VC, Jacobson SG.

Arch Ophthalmol. 2011 Jan;129(1):81-7. doi: 10.1001/archophthalmol.2010.330.


Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remaining.

Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Swider M, Schwartz SB, Banin E, Stone EM.

Invest Ophthalmol Vis Sci. 2011 Jan 5;52(1):70-9. doi: 10.1167/iovs.10-6127.


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