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Akbar Amirfiroozy

Showing results (1-10 of 8) with videos related to

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Molecular Biology Reports|March 6, 2025
Discovering the pathogenesis of a VUS variant in CDH23 associated with sensorineural hearing loss in an Iranian familyMaryam Naghinejad, Sima Mansoori Derakhshan, Sepideh Parvizpour, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 21, 2025
Recent advances in the early detection of ovarian CancerAnahita Soleimani, Akbar Amirfiroozy, Mohammad M Pourseif, et al.
Journal of Human Genetics|April 18, 2025
A random forest-based predictive model for classifying BRCA1 missense variants: a novel approach for evaluating the missense mutations effectHamed Ka, Maryam Naghinejad, Akbar Amirfiroozy, et al.
Molecular Biology Reports|January 17, 2025
The known structural variations in hearing loss and their diagnostic approaches: a comprehensive reviewMaryam Naghinejad, Sepideh Parvizpour, Mahmoud Shekari Khaniani, et al.
Eye (London, England)|May 12, 2021
Association of central serous chorioretinopathy with single nucleotide polymorphisms in complement factor H gene in Iranian populationReza Karkhaneh, Mohsen Toufighi, Akbar Amirfiroozy, et al.
Molecular and Cellular Probes|January 28, 2025
A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patientsAkbar Amirfiroozy, Maryam Naghinejad, Azim Rezamand, et al.
Avicenna Journal of Medical Biotechnology|November 2, 2017
A Novel Mutation in <i>SNX10</i> Gene Causes Malignant Infantile OsteopetrosisAkbar Amirfiroozy, Amir A Hamidieh, Zahra Golchehre, et al.
Molecular Biology Reports|March 27, 2026
Novel compound heterozygous variants in NMNAT1 associated with leber congenital amaurosis: clinical and mutational profilesMoein Kohkalani, Seyyed Amin Seyyed Rezaei, Elaheh Hasani, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Biology Reports|March 6, 2025
Discovering the pathogenesis of a VUS variant in CDH23 associated with sensorineural hearing loss in an Iranian familyMaryam Naghinejad, Sima Mansoori Derakhshan, Sepideh Parvizpour, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 21, 2025
Recent advances in the early detection of ovarian CancerAnahita Soleimani, Akbar Amirfiroozy, Mohammad M Pourseif, et al.
Journal of Human Genetics|April 18, 2025
A random forest-based predictive model for classifying BRCA1 missense variants: a novel approach for evaluating the missense mutations effectHamed Ka, Maryam Naghinejad, Akbar Amirfiroozy, et al.
Molecular Biology Reports|January 17, 2025
The known structural variations in hearing loss and their diagnostic approaches: a comprehensive reviewMaryam Naghinejad, Sepideh Parvizpour, Mahmoud Shekari Khaniani, et al.
Eye (London, England)|May 12, 2021
Association of central serous chorioretinopathy with single nucleotide polymorphisms in complement factor H gene in Iranian populationReza Karkhaneh, Mohsen Toufighi, Akbar Amirfiroozy, et al.
Molecular and Cellular Probes|January 28, 2025
A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patientsAkbar Amirfiroozy, Maryam Naghinejad, Azim Rezamand, et al.
Avicenna Journal of Medical Biotechnology|November 2, 2017
A Novel Mutation in <i>SNX10</i> Gene Causes Malignant Infantile OsteopetrosisAkbar Amirfiroozy, Amir A Hamidieh, Zahra Golchehre, et al.
Molecular Biology Reports|March 27, 2026
Novel compound heterozygous variants in NMNAT1 associated with leber congenital amaurosis: clinical and mutational profilesMoein Kohkalani, Seyyed Amin Seyyed Rezaei, Elaheh Hasani, et al.
Pageof 1