Natario L. Couser

Natario L. Couser

Ophthalmology

1800 Orleans Street
Maumenee Lobby
Baltimore, MD 21287

Last Updated: 09/26/2026

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Found 50 publications

Ocular manifestations of syndromic and ocular-only phenotypes of IFT140-related recessive ciliopathies.

Ocular manifestations of syndromic and ocular-only phenotypes of IFT140-related recessive ciliopathies.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: December 22, 2024

Congenital Myasthenic Syndrome associated with acetylcholine receptor deficiency: case report and review of the literature.

Congenital Myasthenic Syndrome associated with acetylcholine receptor deficiency: case report and review of the literature.

Journal: Ophthalmic genetics

Published: June 04, 2024

Ocular and neurological manifestations of the FDXR-related disorder.

Ocular and neurological manifestations of the FDXR-related disorder.

Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus

Published: May 04, 2024

CO-OCCURRING USHER SYNDROME TYPE 1 AND RENAL FAILURE.

CO-OCCURRING USHER SYNDROME TYPE 1 AND RENAL FAILURE.

Journal: Retinal cases & brief reports

Published: March 12, 2024

Magnetic Resonance Imaging Findings and Genetic Testing Results in Children With Congenital Corneal Opacities.

Magnetic Resonance Imaging Findings and Genetic Testing Results in Children With Congenital Corneal Opacities.

Journal: American journal of ophthalmology

Published: June 29, 2023

NPHP1-Related ciliopathies: A new case and major review of the ophthalmic manifestations of 147 reported cases.

NPHP1-Related ciliopathies: A new case and major review of the ophthalmic manifestations of 147 reported cases.

Journal: Clinical case reports

Published: June 26, 2023

The Role of Genetic Testing in Avoiding Diagnostic Delays in Inherited Retinal Disease.

The Role of Genetic Testing in Avoiding Diagnostic Delays in Inherited Retinal Disease.

Journal: Retinal cases & brief reports

Published: April 28, 2023

Genotype-phenotype analysis of ocular findings in Rubinstein-Taybi syndrome - A case report and review of literature.

Genotype-phenotype analysis of ocular findings in Rubinstein-Taybi syndrome - A case report and review of literature.

Journal: Ophthalmic genetics

Published: April 05, 2023

Facial and ocular manifestations of male patients affected by the HUWE1-related intellectual developmental disorder.

Facial and ocular manifestations of male patients affected by the HUWE1-related intellectual developmental disorder.

Journal: International journal of molecular epidemiology and genetics

Published: March 17, 2023

The epidemiology of strabismus and cataracts within a pediatric population in Saint Vincent and the Grenadines: an analysis of 201 consecutive cases.

The epidemiology of strabismus and cataracts within a pediatric population in Saint Vincent and the Grenadines: an analysis of 201 consecutive cases.

Journal: International journal of molecular epidemiology and genetics

Published: December 22, 2022

C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases.

C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases.

Journal: Clinical case reports

Published: December 20, 2022

A New Case and Comprehensive Review of the Ophthalmic Manifestations of 172 Individuals With Branchio-Oculo-Facial Syndrome.

A New Case and Comprehensive Review of the Ophthalmic Manifestations of 172 Individuals With Branchio-Oculo-Facial Syndrome.

Journal: Journal of pediatric ophthalmology and strabismus

Published: October 20, 2022

Showing 1-12 of 50

Last Updated: 09/26/2026