Search Results - Zein, Wadih M.

Multimodal Evidence of Type 3 Neovascularization in Enhanced S-cone Syndrome by Maldonado, Ramiro S., Zein, Wadih M., Cukras, Catherine

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PARK7-Related Early Onset Parkinson Disease in the Setting of Complete Uniparental Isodisomy of Chromosome 1 by Xiao, Changrui, Markello, Thomas, Zein, Wadih M., Bishop, Rachel, Groden, Catherine, Gahl, William, Toro, Camilo

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Ocular and Systemic Findings in Adults with Uveal Coloboma by Varela, Malena Daich, Huryn, Laryssa A., Hufnagel, Robert B., Zein, Wadih M., Blain, Delphine, Brooks, Brian P.

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Active Cell Appearance Model Induced Generative Adversarial Networks for Annotation-Efficient Cell Segmentation and Identification on Adaptive Optics Retinal Images by Liu, Jianfei, Shen, Christine, Aguilera, Nancy, Cukras, Catherine, Hufnagel, Robert B., Zein, Wadih M., Liu, Tao, Tam, Johnny

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Ophthalmic Manifestations and Long-Term Visual Outcomes in Patients with Cobalamin C Deficiency by Brooks, Brian P., Thompson, Amy H., Sloan, Jennifer, Manoli, Irini, Carrillo-Carrasco, Nuria, Zein, Wadih M., Venditti, Charles P.

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Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy by Pfister, Tyler A., Zein, Wadih M., Cukras, Catherine A., Sen, Hatice N., Maldonado, Ramiro S., Huryn, Laryssa A., Hufnagel, Robert B.

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Genotype-phenotype associations in a large PRPH2-related retinopathy cohort by Reeves, Melissa J., Goetz, Kerry E., Guan, Bin, Ullah, Ehsan, Blain, Delphine, Zein, Wadih M., Tumminia, Santa J., Hufnagel, Robert B.

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Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to Khan by Pineda-Alvarez, Daniel E., Solomon, Benjamin D., Roessler, Erich, Balog, Joan Z., Hadley, Donald W., Zein, Wadih M., Brooks, Brian P., Muenke, Maximilian

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BRITTLE HAIR, DEVELOPMENTAL DELAY, NEUROLOGIC ABNORMALITIES AND PHOTOSENSITIVITY IN A 4 YEAR OLD GIRL by Zhou, Xiaolong, Khan, Sikandar G., Tamura, Deborah, Patronas, Nicholas J., Zein, Wadih M., Brooks, Brian P., Kraemer, Kenneth H., DiGiovanna, John J.

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Applying next generation sequencing with microdroplet PCR to determine the disease-causing mutations in retinal dystrophies by Wang, Xinjing, Zein, Wadih M., D’Souza, Leera, Roberson, Chimere, Wetherby, Keith, He, Hong, Villarta, Angela, Turriff, Amy, Johnson, Kory R., Fann, Yang C.

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Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort by Serpen, Jasmine Y., Prasov, Lev, Zein, Wadih M., Cukras, Catherine A., Cunningham, Denise, Murphy, Elizabeth C., Turriff, Amy, Brooks, Brian P., Huryn, Laryssa A.

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A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching by Wang, Chen, Brancusi, Flavia, Anderson, Michael G, Cunningham, Denise, Hedberg-Buenz, Adam, Simeonov, Dimitre, Gahl, William A, Zein, Wadih M, Adams, David R, Brooks, Brian

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DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature by Meissner, Laura E., Macnamara, Ellen F., D'Souza, Precilla, Yang, John, Vezina, Gilbert, Ferreira, Carlos R., Zein, Wadih M., Tifft, Cynthia J., Adams, David R.

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A sialidosis type I cohort and a quantitative approach to multimodal ophthalmic imaging of the macular cherry-red spot by Daich Varela, Malena, Zein, Wadih M, Toro, Camilo, Groden, Catherine, Johnston, Jean, Huryn, Laryssa A, d’Azzo, Alessandra, Tifft, Cynthia J, FitzGibbon, Edmond J

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A Broad Range of Ophthalmologic Anomalies is Part of the Holoprosencephaly Spectrum by Pineda-Alvarez, Daniel E., Solomon, Benjamin D., Roessler, Erich, Balog, Joan Z., Hadley, Donald W., Zein, Wadih M., Hadsall, Casey K., Brooks, Brian P., Muenke, Maximilian

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The peroxisomal disorder spectrum and Heimler syndrome: Deep phenotyping and review of the literature by Varela, Malena Daich, Jani, Priyam, Zein, Wadih M., D'Souza, Precilla, Wolfe, Lynne, Chisholm, Jennifer, Zalewski, Christopher, Adams, David, Warner, Blake M., Huryn, Laryssa A., Hufnagel, Robert B.

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Systematic analysis of physical examination characteristics of 94 individuals with Joubert syndrome: Keys to suspecting the diagnosis by Forsyth, RaeLynn, Parisi, Melissa A., Altintas, Burak, Malicdan, May Christine, Vilboux, Thierry, Knoll, Jasmine, Brooks, Brian P., Zein, Wadih M., Gahl, William A., Toro, Camilo, Gunay-Aygun, Meral

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CNGB3-Achromatopsia Clinical Trial With CNTF: Diminished Rod Pathway Responses With No Evidence of Improvement in Cone Function by Zein, Wadih M., Jeffrey, Brett G., Wiley, Henry E., Turriff, Amy E., Tumminia, Santa J., Tao, Weng, Bush, Ronald A., Marangoni, Dario, Wen, Rong, Wei, Lisa L., Sieving, Paul A.

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Atypical and Ultra-rare Usher Syndrome: A Review by Nolen, Rosalie M., Hufnagel, Robert B., Friedman, Thomas B., Turriff, Amy E., Brewer, Carmen C., Zalewski, Christopher K., King, Kelly A., Wafa, Talah, Griffith, Andrew J., Brooks, Brian, Zein, Wadih M.

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Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies by Malechka, Volha V., Cukras, Catherine A., Chew, Emily Y., Sergeev, Yuri V., Blain, Delphine, Jeffrey, Brett G., Ullah, Ehsan, Hufnagel, Robert B., Brooks, Brian P., Huryn, Laryssa A., Zein, Wadih M.

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