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The British Journal of Ophthalmology
|
August 6, 2020
A sialidosis type I cohort and a quantitative approach to multimodal ophthalmic imaging of the macular cherry-red spot
Malena Daich Varela, Wadih M Zein, Camilo Toro, et al.
British Journal of Biomedical Science
|
September 4, 2018
Association of genetic polymorphisms of chemokines and their receptors with clearance or persistence of hepatitis C virus infection
M El-Bendary, M Neamatallah, H Elalfy, et al.
Evaluation and Program Planning
|
November 28, 2022
Promoting the culture of key performance indicators (KPIs) among primary health care staff at health district level: An intervention study
Madiha Said Mohamed Abdel-Razik, Hoda Ibrahim Rizk, Marwa M Zein, et al.
Molecular Imaging
|
March 22, 2021
Use of Innovative SPECT Techniques in the Presurgical Evaluation of Patients with Nonlesional Extratemporal Drug-Resistant Epilepsy
Ahmed Yassin, Khalid El-Salem, Abdel-Hameed Al-Mistarehi, et al.
Molecular Genetics & Genomic Medicine
|
November 7, 2020
DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature
Laura E Meissner, Ellen F Macnamara, Precilla D'Souza, et al.
Journal of Ophthalmology
|
October 21, 2020
Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort
Jasmine Y Serpen, Lev Prasov, Wadih M Zein, et al.
Translational Vision Science & Technology
|
June 6, 2025
Electroretinography With the RM Electrode: Normative Reference Ranges, Variation With Age, and Comparison With the Burian-Allen Electrode
Brett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Retina (Philadelphia, Pa.)
|
March 13, 2024
OUTER RETINAL MICROCAVITATIONS IN RETINITIS PIGMENTOSA : A Novel Optical Coherence Tomography Finding Common in RP1 -Related Retinopathy
Ioannis S Dimopoulos, Laryssa A Huryn, Robert B Hufnagel, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2011
A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum
Daniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Translational Vision Science & Technology
|
September 3, 2024
Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans
Agnes C Owete, Raisa Ionin, Laryssa A Huryn, et al.
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of 13
Search research articles
Search
Showing results (51-60 of 130) with videos related to
Sort By:
Page
of 13
The British Journal of Ophthalmology
|
August 6, 2020
A sialidosis type I cohort and a quantitative approach to multimodal ophthalmic imaging of the macular cherry-red spot
Malena Daich Varela, Wadih M Zein, Camilo Toro, et al.
British Journal of Biomedical Science
|
September 4, 2018
Association of genetic polymorphisms of chemokines and their receptors with clearance or persistence of hepatitis C virus infection
M El-Bendary, M Neamatallah, H Elalfy, et al.
Evaluation and Program Planning
|
November 28, 2022
Promoting the culture of key performance indicators (KPIs) among primary health care staff at health district level: An intervention study
Madiha Said Mohamed Abdel-Razik, Hoda Ibrahim Rizk, Marwa M Zein, et al.
Molecular Imaging
|
March 22, 2021
Use of Innovative SPECT Techniques in the Presurgical Evaluation of Patients with Nonlesional Extratemporal Drug-Resistant Epilepsy
Ahmed Yassin, Khalid El-Salem, Abdel-Hameed Al-Mistarehi, et al.
Molecular Genetics & Genomic Medicine
|
November 7, 2020
DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature
Laura E Meissner, Ellen F Macnamara, Precilla D'Souza, et al.
Journal of Ophthalmology
|
October 21, 2020
Clinical Features of Optic Disc Drusen in an Ophthalmic Genetics Cohort
Jasmine Y Serpen, Lev Prasov, Wadih M Zein, et al.
Translational Vision Science & Technology
|
June 6, 2025
Electroretinography With the RM Electrode: Normative Reference Ranges, Variation With Age, and Comparison With the Burian-Allen Electrode
Brett G Jeffrey, Xueyang Yin, Christina Appleman, et al.
Retina (Philadelphia, Pa.)
|
March 13, 2024
OUTER RETINAL MICROCAVITATIONS IN RETINITIS PIGMENTOSA : A Novel Optical Coherence Tomography Finding Common in RP1 -Related Retinopathy
Ioannis S Dimopoulos, Laryssa A Huryn, Robert B Hufnagel, et al.
American Journal of Medical Genetics. Part A
|
October 7, 2011
A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum
Daniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Translational Vision Science & Technology
|
September 3, 2024
Seeing in Color: Inclusion and Characterization of Hereditary Eye Disease in African Americans
Agnes C Owete, Raisa Ionin, Laryssa A Huryn, et al.
Page
of 13