1. Healthcare recommendations for Joubert syndrome. Issue 1 (11th November 2019) Authors: Bachmann‐Gagescu, Ruxandra; Dempsey, Jennifer C.; Bulgheroni, Sara; Chen, Maida L.; D'Arrigo, Stefano; Glass, Ian A.; Heller, Theo; Héon, Elise; Hildebrandt, Friedhelm; Joshi, Nirmal; Knutzen, Dana; Kroes, Hester Y.; Mack, Stephen H.; Nuovo, Sara; Parisi, Melissa A.; Snow, Joseph; Summers, Angela... Journal: American journal of medical genetics Issue: Volume 182:Issue 1(2020) Page Start: 229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Hey, I Just Did a New Operation!. Issue 1 (January 2015) Authors: Sagar, Stephen P.; Law, Peggy W.; Shaul, Randi Zlotnik; Héon, Elise; Langer, Jacob C.; Wright, James G. Journal: Annals of surgery Issue: Volume 261:Issue 1(2015:Jan.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hey, I Just Did a New Operation!: Introducing Innovative Procedures and Devices Within an Academic Health Center. Issue 1 (January 2015) Authors: Sagar, Stephen P.; Law, Peggy W.; Shaul, Randi Zlotnik; Héon, Elise; Langer, Jacob C.; Wright, James G. Journal: Annals of surgery Issue: Volume 261:Issue 1(2015:Jan.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. In Memoriam Maria Musarella. (September 2014) Authors: Héon, Elise; Levin, Alex; MacDonald, Ian M. Journal: Ophthalmic genetics Issue: Volume 35:Number 3(2014:Sep.) Page Start: 129 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Molecular characterisation of congenital glaucoma in a consanguineous Canadian community: a step towards preventing glaucoma related blindness. Issue 6 (1st June 2000) Authors: Martin, S Nicole; Sutherland, Joanne; Levin, Alex V; Klose, Robert; Priston, Megan; Héon, Elise Journal: Journal of medical genetics Issue: Volume 37:Issue 6(2000) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Molecular testing prognostic of low risk in epithelioid uveal melanoma in a child. Issue 3 (3rd January 2013) Authors: Dimaras, Helen; Parulekar, Manoj Vijay; Kwok, Grace; Simpson, E Rand; Ali, Asim; Halliday, William; Shago, Mary; Harbour, J William; Héon, Elise; Gallie, Brenda L; Chan, Helen S L Journal: British journal of ophthalmology Issue: Volume 97:Issue 3(2013) Page Start: 323 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population. Issue 7 (14th May 2010) Authors: Billingsley, Gail; Bin, Jenea; Fieggen, Karen J; Duncan, Jacque L; Gerth, Christina; Ogata, Koji; Wodak, Shoshana S; Traboulsi, Elias I; Fishman, Gerald A; Paterson, Andrew; Chitayat, David; Knueppel, Tanja; Millán, José M; Mitchell, Grant A; Deveault, Catherine; Héon, Elise Journal: Journal of medical genetics Issue: Volume 47:Issue 7(2010) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium. Issue 12 (7th October 2014) Authors: Vincent, Ajoy; Forster, Nicole; Maynes, Jason T; Paton, Tara A; Billingsley, Gail; Roslin, Nicole M; Ali, Arfan; Sutherland, Joanne; Wright, Tom; Westall, Carol A; Paterson, Andrew D; Marshall, Christian R; Héon, Elise Other Names: Boycott Kym author non-byline.; Friedman Jan author non-byline.; Michaud Jacques author non-byline.; Bernier Francois author non-byline.; Brudno Michael author non-byline.; Fernandez Bridget author non-byline.; Knoppers Bartha author non-byline.; Samuels Mark author non-byline.; Scherer Stephen a... Journal: Journal of medical genetics Issue: Volume 51:Issue 12(2014) Page Start: 797 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives. (July 2020) Authors: Garafalo, Alexandra V.; Cideciyan, Artur V.; Héon, Elise; Sheplock, Rebecca; Pearson, Alexander; WeiYang Yu, Caberry; Sumaroka, Alexander; Aguirre, Gustavo D.; Jacobson, Samuel G. Journal: Progress in retinal and eye research Issue: Volume 77(2020:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Retinal degeneration in autoimmune polyglandular syndrome type 1: a case series. Issue 11 (29th April 2015) Authors: Bourgault, Serge; Baril, Catherine; Vincent, Ajoy; Héon, Elise; Ali, Asim; MacDonald, Ian; Lueder, Gregg T; Colleaux, Kevin M; Laliberté, Isabelle Journal: British journal of ophthalmology Issue: Volume 99:Issue 11(2015) Page Start: 1536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗