Search Results - "Ledoux, Danielle M"

  • Showing 1 - 13 results of 13
Refine Results
  1. 1

    Down syndrome: a review of ocular manifestations by Haseeb, Abid, Huynh, Elisah, ElSheikh, Reem H., ElHawary, Ahmed S., Scelfo, Christina, Ledoux, Danielle M., Maidana, Daniel E., Elhusseiny, Abdelrahman M.

    Published in Therapeutic Advances in Ophthalmology (01-01-2022)
    “…Down syndrome is the most common genetically mediated intellectual disability. Although many physiologic and pathologic features of Down syndrome are discussed…”
    Get full text
    Book Review Journal Article
  2. 2

    Optic Nerve Appearance in Patients With Down Syndrome by Schneier, Andrew J, Heidary, Gena, Ledoux, Danielle M

    “…To the Editors: Children with Down syndrome (DS) are commonly seen by pediatric ophthalmologists because significant ocular conditions are associated with the…”
    Get full text
    Journal Article
  3. 3

    Pediatric cataract extraction with intraocular lens implantation: Visual acuity outcome when measured at age four years and older by Ledoux, Danielle M., MD, Trivedi, Rupal H., MD, MSCR, Wilson, M. Edward, MD, Payne, John F., MD

    Published in Journal of AAPOS (01-06-2007)
    “…Purpose Assessment of visual outcome of pediatric eyes that underwent cataract extraction with primary intraocular lens (IOL) implantation at a single center…”
    Get full text
    Journal Article
  4. 4

    In vivo quasi-elastic light scattering detects molecular changes in the lenses of adolescents with Down syndrome by Sarangi, Srikant, Minaeva, Olga, Ledoux, Danielle M., Parsons, Douglas S., Moncaster, Juliet A., Black, Caitlin A., Hollander, Jeffrey, Tripodis, Yorghos, Clark, John I., Hunter, David G., Goldstein, Lee E.

    Published in Experimental eye research (01-04-2024)
    “…Down syndrome (DS) is the most common chromosomal disorder in humans. DS is associated with increased prevalence of several ocular sequelae, including…”
    Get full text
    Journal Article
  5. 5
  6. 6
  7. 7
  8. 8

    Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders by Jurgens, Julie A., Barry, Brenda J., Chan, Wai-Man, MacKinnon, Sarah, Matos Ruiz, Paola M., England, Eleina M., Pais, Lynn, Groopman, Emily, Russell, Kathryn A., Di Gioia, Silvio Alessandro, Lee, Arthur S., Shaaban, Sherin, Bekele, Sarah, Toffoloni, Melissa, Foster, Emma E., Berube, Lindsay, Rivera-Quiles, Cristina, Mensching, Fiona M., Sanchis-Juan, Alba, Fu, Jack M., Wong, Isaac, Zhao, Xuefang, Wilson, Michael W., Lek, Monkol, Abarca-Barriga, Hugo, Al-Haddad, Christiane, Chacon-Camacho, Oscar Francisco, Chang, Lan, Christiansen, Stephen P., Ciccarelli, Maria Laura, Cordonnier, Monique, Cox, Gerald F., Curry, Cynthia J., Lee Dahm, Thomas, David, Karen L., De Berardinis, Teresa, Demer, Joseph L., Drack, Arlene V., Eggenberger, Eric, Elder, James E., Elliott, Alexandra T., Epley, K. David, Feldman, Hagit Baris, Ferreira, Carlos R., Gerth-Kahlert, Christina, Halliday, Dorothy J., Hanisch, Frank, Hay, Eleanor, Holder, Christopher, Iannaccone, Alessandro, Isenberg, Sherwin J., Kahana, Alon, Kazlas, Melanie, Kerr, Natalie C., Ko, Melissa W., Koc, Feray, Larsen, Dorte Ancher, Lay-Son, Guillermo, Ledoux, Danielle M., Levin, Alex V., Levy, Richard L., Mackey, David A., Mantagos, Iason S., Marti, Candice, Menezes, Manoj P., Mikail, Claudia N., Miller, Kathryn Bisceglia, Miyana, Kaori, Mullineaux, Lisa, Nishimura, Julie K., Noble, A. Gwendolyn, Pavone, Piero, Phalen, James A., Poduri, Annapurna, Polo, Claudia R., Prasov, Lev, Ramos, Feliciano J., Ramos-Caceres, Maria, Robb, Richard M., Rossillion, Béatrice, Smith, Lois E.H., Sorkin, Jeffrey A., Soul, Janet S., Stalker, Heather J., Stasheff, Steven F., Strassberg, Sonya, Thomas, Ioan Talfryn, VanderVeen, Deborah K., Vincent, Andrea L., Wabbels, Bettina, Wong, Agnes M.F., Wu, Carolyn, Yeung, Alison, Young, Terri L., Zwaan, Johan, Brand, Harrison, Talkowski, Michael E., MacArthur, Daniel G., Robson, Caroline D., Engle, Elizabeth C.

    Published in Genetics in medicine (17-07-2024)
    “…To identify genetic etiologies and genotype/phenotype associations for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs). We coupled…”
    Get full text
    Journal Article
  9. 9
  10. 10
  11. 11
  12. 12

    What’s Your Diagnosis? by Ledoux, Danielle M., Walton, David S.

    “…When the patient was 5 months old, his mother noticed a color change in his right eye. She described that the iris had become "less blue" than his left eye…”
    Get full text
    Journal Article
  13. 13