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Melanie A Schmitt

Showing results (1-10 of 8) with videos related to

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Journal of Binocular Vision and Ocular Motility|November 18, 2020
Impact of Amblyopia on the Central Nervous SystemNathaniel P Miller, Breanna Aldred, Melanie A Schmitt, et al.
Investigative Ophthalmology & Visual Science|February 17, 2018
Retinothalamic White Matter Abnormalities in AmblyopiaBrian Allen, Melanie A Schmitt, Burton J Kushner, et al.
Retina (Philadelphia, Pa.)|August 18, 2022
TOPICAL CARBONIC ANHYDRASE INHIBITORS IN THE LONG-TERM TREATMENT OF JUVENILE X-LINKED RETINOSCHISISMelanie A Schmitt, Kevin Wang, Meghan J DeBenedictis, et al.
American Journal of Ophthalmology Case Reports|September 18, 2020
Ocular evaluation and genetic test for an early Alström Syndrome diagnosisTyler Etheridge, Elizabeth R Kellom, Rachel Sullivan, et al.
WMJ : Official Publication of the State Medical Society of Wisconsin|January 7, 2026
Characteristics and Predictors of Pediatric and Adult Patients with Inherited Retinal Degenerations: Tertiary Care Ophthalmology Clinic DataMelissa A Trudrung, Matthew T McLaughlin, Caleb P Ganansky, et al.
Plos One|November 3, 2022
Reliability of COVID-19 data: An evaluation and reflectionApril R Miller, Samin Charepoo, Erik Yan, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019
Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task ForceArlene V Drack, Virginia Miraldi Utz, Kai Wang, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of Binocular Vision and Ocular Motility|November 18, 2020
Impact of Amblyopia on the Central Nervous SystemNathaniel P Miller, Breanna Aldred, Melanie A Schmitt, et al.
Investigative Ophthalmology & Visual Science|February 17, 2018
Retinothalamic White Matter Abnormalities in AmblyopiaBrian Allen, Melanie A Schmitt, Burton J Kushner, et al.
Retina (Philadelphia, Pa.)|August 18, 2022
TOPICAL CARBONIC ANHYDRASE INHIBITORS IN THE LONG-TERM TREATMENT OF JUVENILE X-LINKED RETINOSCHISISMelanie A Schmitt, Kevin Wang, Meghan J DeBenedictis, et al.
American Journal of Ophthalmology Case Reports|September 18, 2020
Ocular evaluation and genetic test for an early Alström Syndrome diagnosisTyler Etheridge, Elizabeth R Kellom, Rachel Sullivan, et al.
WMJ : Official Publication of the State Medical Society of Wisconsin|January 7, 2026
Characteristics and Predictors of Pediatric and Adult Patients with Inherited Retinal Degenerations: Tertiary Care Ophthalmology Clinic DataMelissa A Trudrung, Matthew T McLaughlin, Caleb P Ganansky, et al.
Plos One|November 3, 2022
Reliability of COVID-19 data: An evaluation and reflectionApril R Miller, Samin Charepoo, Erik Yan, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019
Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task ForceArlene V Drack, Virginia Miraldi Utz, Kai Wang, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
Pageof 1