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IEEE Journal of Biomedical and Health Informatics
|
June 25, 2026
Multimodal Bidirectional Direct Preference Optimization and Instruction Fine-Tuning for Medical Image Understanding and Generation
Jun Lyu, Zhihao Luo, Selwa A F Al-Hazzaa, et al.
IEEE Journal of Biomedical and Health Informatics
|
August 25, 2025
TransSeg: Leveraging Transformer with Channel-Wise Attention and Semantic Memory for Semi-Supervised Ultrasound Segmentation
Jun Lyu, Liangjiang Li, Selwa A F Al-Hazzaa, et al.
IEEE Journal of Biomedical and Health Informatics
|
August 22, 2025
Dual-MFNet: AI-Driven Dual-Scale Multimodal Fusion With State Space Networks for Personalized MRI Synthesis
Jun Lyu, Xiudong Chen, M Shamim Hossain, et al.
American Journal of Human Genetics
|
March 5, 2013
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia
Fatema Zahrani, Mohammed A Aldahmesh, Muneera J Alshammari, et al.
The American Journal of Case Reports
|
April 7, 2020
Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series
Qais S Dirar, Hebah M Musalem, Selwa A F Al-Hazzaa, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 9, 2014
COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family
Khushnooda Ramzan, Faiqa Imtiaz, Khalid Taibah, et al.
The American Journal of Case Reports
|
April 29, 2018
Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center
Hebah M Musalem, Qais S Dirar, Selwa A F Al-Hazzaa, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 2, 2018
Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations
Khushnooda Ramzan, Mohammed Al-Owain, Rozeena Huma, et al.
Frontiers in Medicine
|
December 11, 2023
The application of artificial intelligence in diabetic retinopathy screening: a Saudi Arabian perspective
Abdulaziz A Barakat, Omar Mobarak, Haroon Ahmed Javaid, et al.
Genes
|
December 15, 2020
Identification of Novel <i>CDH23</i> Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss
Khushnooda Ramzan, Nouf S Al-Numair, Sarah Al-Ageel, et al.
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Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
IEEE Journal of Biomedical and Health Informatics
|
June 25, 2026
Multimodal Bidirectional Direct Preference Optimization and Instruction Fine-Tuning for Medical Image Understanding and Generation
Jun Lyu, Zhihao Luo, Selwa A F Al-Hazzaa, et al.
IEEE Journal of Biomedical and Health Informatics
|
August 25, 2025
TransSeg: Leveraging Transformer with Channel-Wise Attention and Semantic Memory for Semi-Supervised Ultrasound Segmentation
Jun Lyu, Liangjiang Li, Selwa A F Al-Hazzaa, et al.
IEEE Journal of Biomedical and Health Informatics
|
August 22, 2025
Dual-MFNet: AI-Driven Dual-Scale Multimodal Fusion With State Space Networks for Personalized MRI Synthesis
Jun Lyu, Xiudong Chen, M Shamim Hossain, et al.
American Journal of Human Genetics
|
March 5, 2013
Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia
Fatema Zahrani, Mohammed A Aldahmesh, Muneera J Alshammari, et al.
The American Journal of Case Reports
|
April 7, 2020
Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series
Qais S Dirar, Hebah M Musalem, Selwa A F Al-Hazzaa, et al.
International Journal of Pediatric Otorhinolaryngology
|
January 9, 2014
COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family
Khushnooda Ramzan, Faiqa Imtiaz, Khalid Taibah, et al.
The American Journal of Case Reports
|
April 29, 2018
Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center
Hebah M Musalem, Qais S Dirar, Selwa A F Al-Hazzaa, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 2, 2018
Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations
Khushnooda Ramzan, Mohammed Al-Owain, Rozeena Huma, et al.
Frontiers in Medicine
|
December 11, 2023
The application of artificial intelligence in diabetic retinopathy screening: a Saudi Arabian perspective
Abdulaziz A Barakat, Omar Mobarak, Haroon Ahmed Javaid, et al.
Genes
|
December 15, 2020
Identification of Novel <i>CDH23</i> Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss
Khushnooda Ramzan, Nouf S Al-Numair, Sarah Al-Ageel, et al.
Page
of 2