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Dive into the research topics where Natario Couser is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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A NOVEL PATHOGENIC VARIANT OF THE PRPH2 GENE IN MULTIFOCAL PATTERN DYSTROPHY SIMULATING STARGARDT DISEASE: A CASE REPORT AND MAJOR REVIEW
Alsumait, A., Mahmoudzadeh, R. & Couser, N., Jul 1 2025, In: Retinal Cases and Brief Reports. 19, 4, p. 476-484 9 p.Research output: Contribution to journal › Article › peer-review
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CO-OCCURRING USHER SYNDROME TYPE 1 AND RENAL FAILURE
Le, H., Anderson, H., Lopez, G., Bayer-Vile, J., Al-Saif, H. & Couser, N., May 1 2025, In: Retinal Cases and Brief Reports. 19, 3, p. 379-385 7 p.Research output: Contribution to journal › Article › peer-review
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Ocular and neurological manifestations of the FDXR-related disorder
Kaler, A. & Couser, N., Feb 2025, In: Journal of AAPOS. 29, 1, 104102.Research output: Contribution to journal › Article › peer-review
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Ocular manifestations of syndromic and ocular-only phenotypes of IFT140-related recessive ciliopathies
Kaler, A., Lal, V., Kumar, V., Gulhar, S. & Couser, N., Aug 2025, In: Journal of AAPOS. 29, 4, 104281.Research output: Contribution to journal › Article › peer-review
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Congenital Myasthenic Syndrome associated with acetylcholine receptor deficiency: case report and review of the literature
Batheja, A., Bayer-Vile, J., Silverstein, E. & Couser, N., 2024, In: Ophthalmic Genetics. 45, 5, p. 481-487 7 p.Research output: Contribution to journal › Article › peer-review
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