Natario L Couser (Natario Couser)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 26

Top Venues

Ophthalmic genetics

Case reports in genetics

American journal of medical genetics. Part A

Clinical case reports

Johns Hopkins University (MSC)

This page only lists publications with an associated author ORCID identifier.

Education History

Johns Hopkins University

United States

MSC

University of Virginia

United States

BSC

Publications

Aashish Batheja, Julie Bayer-Vile, Evan Silverstein, Natario L Couser
Congenital Myasthenic Syndrome associated with acetylcholine receptor deficiency: case report and review of the literature. Ophthalmic genetics (2024)
Hong Le, Helen Anderson, Glydel Lopez, Julie Bayer-Vile, Hind Al-Saif, Natario L Couser
Co-occurring Usher syndrome Type 1 and Renal Failure. Retinal cases & brief reports (2024)
Eva Jin, Hong Le, Ann Jewell, Natario L Couser
Genotype-phenotype analysis of ocular findings in Rubinstein-Taybi syndrome - A case report and review of literature. Ophthalmic genetics (2023)
Arth H Shah, Elisse Park, Tammy Luke, Qingguo Xu, Ann Jewell, Natario L Couser
The Role of Genetic Testing in Avoiding Diagnostic Delays in Inherited Retinal Disease. Retinal cases & brief reports (2023)
Hong Le, Eva Jin, Ann Jewell, Colleen Jackson-Cook, Gloria T Haskell, Natario L Couser
Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features. American journal of medical genetics. Part A (2023)
Meagan Shinbashi, Ann Jewell, Jessica Randolph, Natario L Couser
C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases. Clinical case reports 11 (3) (2023)
Meagan Shinbashi, Ann Jewell, Jessica Randolph, Natario L Couser
C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases. Clinical case reports 11 (3) (2023)
Kevin Babu, Kimberly Seamon, Ann Jewell, Anna Harrison, Amy Harper, Hind Al Saif, Natario L Couser
Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review. Ophthalmic genetics (2022)
Stephanie Saadeh-Jackson, Linnet Rodriguez, Christopher T Leffler, Casey Freymiller, Elizabeth Wolf, Niran Wijesooriya, Natario L Couser
Ophthalmia neonatorum due to Escherichia coli : A rare cause or an emerging bacterial etiology of neonatal conjunctivitis? Clinical case reports 10 (8) (2022)
Gracia Luoma-Overstreet, Ann Jewell, Vikram Brar, Natario L Couser
Occult Macular Dystrophy: a case report and major review. Ophthalmic genetics 43 (5) (2022)
Russell Simmers, Allison Goodwin, Hind Al Saif, Natario L Couser
Ophthalmologic and facial abnormalities of Nicolaides-Baraitser syndrome. Ophthalmic genetics 43 (5) (2022)
Shripadh Chitta, Jineet Patel, Shravan Renapurkar, Christopher Loschiavo, Jennifer Rhodes, Kayla King, Kimberly Salkey, Natario L Couser
Nevoid basal cell carcinoma syndrome: a case report and literature review. Ophthalmic genetics (2021)
Natario L Couser, Brian P Brooks, Arlene V Drack, Suma P Shankar
The evolving role of genetics in ophthalmology. Ophthalmic genetics 42 (2) (2021)
Jamie H Choi, Rachel Li, Rachel Gannaway, Tahnee N Causey, Anna Harrison, Natario L Couser
Corrigendum #2 to "Eye Manifestations of Shprintzen-Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review". Case reports in genetics 2021 (2021)
Arth H Shah, Monika Bapna, Hind Al-Saif, Rachel Li, Natario L Couser
Eye and ocular adnexa manifestations of MED12-related disorders. Ophthalmic genetics (2021)
Linnet Rodriguez, Julia Michelle White, Nikisha Q Richards, Alan X You, Natario L Couser
An Adult Loa loa Worm in the Upper Eyelid: An Atypical Presentation of Loiasis in the United States. Case reports in ophthalmological medicine 2021 (2021)
Virang Kumar, Natario L Couser, Arti Pandya
Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases. Case reports in ophthalmological medicine 2020 (2020)
Jamie H Choi, Rachel Li, Rachel Gannaway, Tahnee N Causey, Anna Harrison, Natario L Couser
Corrigendum to "Eye Manifestations of Shprintzen-Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review". Case reports in genetics 2020 (2020)
Cybil S Stingl, Colleen K Jackson-Cook, Natario L Couser
Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review. Case reports in pediatrics 2020 (2020)
Jamie H Choi, Rachel Li, Rachel Gannaway, Tahnee N Causey, Anna Harrison, Natario L Couser
Eye Manifestations of Shprintzen-Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review. Case reports in genetics 2020 (2020)
David C Gibson, Natario L Couser, Kayla B King
Co-occurrence of incontinentia pigmenti and down syndrome: examining patients' potential susceptibility to autoimmune disease, autoinflammatory disease, cancer, and significant ocular disease. Ophthalmic genetics 42 (1) (2020)
Angela S Gupta, Hind Al Saif, Jennifer M Lent, Natario L Couser
Ocular Manifestations of the NAA10-Related Syndrome. Case reports in genetics 2019 (2019)
Natario L Couser, Debra Keelean-Fuller, Marsha L Davenport, Eden Haverfield, Maheer M Masood, Mark Henin, Arthur S Aylsworth
Cleft palate and hypopituitarism in a patient with Noonan-like syndrome with loose anagen hair-1. American journal of medical genetics. Part A 176 (9) (2018)
Dev Ram Sahni, Michael Wallace, Mansi Kanhere, Hind Al Saif, Natario L Couser
A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations. Case reports in ophthalmological medicine 2018 (2018)
Natario L Couser, Daniel S Marchuk, Laurie D Smith, Alexandra Arreola, Kathleen A Kaiser-Rogers, Joseph Muenzer, Arti Pandya, Muge Gucsavas-Calikoglu, Cynthia M Powell
Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome. American journal of medical genetics. Part A 173 (10) (2017)
Natario L Couser, Maheer M Masood, Arthur S Aylsworth, Roger E Stevenson
Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic genetics 38 (5) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Natario L Couser (Natario Couser)