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Results: 1 to 20 of 77

1.

Maternal placentophagy as an alternative medicinal practice in the postpartum period.

Schwartz S.

Midwifery Today Int Midwife. 2014 Summer;(110):28-9. No abstract available.

PMID:
25112065
[PubMed - in process]
2.

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.

PMID:
25074776
[PubMed - in process]
3.

The authors respond.

Gatto NM, Campbell UB, Schwartz S.

Epidemiology. 2014 Jul;25(4):619-20. doi: 10.1097/EDE.0000000000000125. No abstract available.

PMID:
24887170
[PubMed - in process]
4.

The Role of Help-Seeking in Preventing Suicide Attempts among Lesbians, Gay Men, and Bisexuals.

Meyer IH, Teylan M, Schwartz S.

Suicide Life Threat Behav. 2014 May 14. doi: 10.1111/sltb.12104. [Epub ahead of print]

PMID:
24825437
[PubMed - as supplied by publisher]
5.

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.

PMID:
24550365
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

An organizational schema for epidemiologic causal effects.

Gatto NM, Campbell UB, Schwartz S.

Epidemiology. 2014 Jan;25(1):88-97. doi: 10.1097/EDE.0000000000000005.

PMID:
24276524
[PubMed - indexed for MEDLINE]
7.

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.

PMID:
24067079
[PubMed - indexed for MEDLINE]
8.

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.

PMID:
23341635
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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.

PMID:
23341016
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

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.

PMID:
23246293
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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.

PMID:
23150612
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

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.

PMID:
23035049
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
22807293
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Extending the sufficient component cause model to describe the Stable Unit Treatment Value Assumption (SUTVA).

Schwartz S, Gatto NM, Campbell UB.

Epidemiol Perspect Innov. 2012 Apr 3;9:3. doi: 10.1186/1742-5573-9-3.

PMID:
22472125
[PubMed]
Free PMC Article
15.

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.

PMID:
22247458
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

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.

PMID:
22142163
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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.

PMID:
22110072
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

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.

PMID:
21911650
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

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.

PMID:
21873662
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Transportability and causal generalization.

Schwartz S, Gatto NM, Campbell UB.

Epidemiology. 2011 Sep;22(5):745-6. doi: 10.1097/EDE.0b013e3182254b8f. No abstract available.

PMID:
21811113
[PubMed - indexed for MEDLINE]

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