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You searched for: Author/Creator Aleman, Tomas S.

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1. Absent Foveal Pit, Also Known as Fovea Plana, in a Child without Associated Ocular or Systemic Findings. (26th July 2018)

2. Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model. (4th May 2021)

3. Charcot–Marie–Tooth Disease Associated With a Novel Mutation in MFN2 Presenting With Subacute Vision Loss. Issue 1 (16th March 2022)

4. Charcot–Marie–Tooth Disease Associated With a Novel Mutation in MFN2 Presenting With Subacute Vision Loss. Issue 1 (March 2022)

5. DANON DISEASE: A MODEL OF PHOTORECEPTOR DEGENERATION SECONDARY TO PRIMARY RETINAL PIGMENT EPITHELIUM DISEASE. Issue Volume 16:Issues 6(2022) (November 2022)

6. Detailed functional and structural phenotype of Bietti crystalline dystrophy associated with mutations in CYP4V2 complicated by choroidal neovascularization. (1st October 2016)