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Asad Munir

Showing results (1-10 of 14) with videos related to

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Plos One|January 30, 2018
Hybrid two-stage active contour method with region and edge information for intensity inhomogeneous image segmentationShafiullah Soomro, Asad Munir, Kwang Nam Choi
BMC Ophthalmology|February 5, 2024
A systematic review of inherited retinal dystrophies in Pakistan: updates from 1999 to April 2023Asad Munir, Salma Afsar, Atta Ur Rehman
Materials (Basel, Switzerland)|February 11, 2023
Effect of Short-Term Ageing Treatment on Bending Force Behavior of Commercial Nickel-Titanium ArchwireAsad Munir, Muhammad Fauzinizam Razali, Muhammad Hafiz Hassan, et al.
Annals of Medicine|March 3, 2025
Exome sequencing identifies a homozygous splice site variant in <i>RP1</i> as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani familyAbdur Rashid, Asad Munir, Muhammad Zahid, et al.
Computational and Mathematical Methods in Medicine|September 21, 2017
Segmentation of Left and Right Ventricles in Cardiac MRI Using Active ContoursShafiullah Soomro, Farhan Akram, Asad Munir, et al.
Cureus|February 16, 2026
Negative Appendectomy Rates and Their Correlation With the Use of Histopathology: A Clinical AuditJamshid Khan, Yasir Hakim, Aalia Amjad, et al.
Cureus|March 23, 2021
Comparison of Urethrocutaneous Fistula Rate After Single Dartos and Double Dartos Tubularized Incised Plate Urethroplasty in Pediatric HypospadiasFatima Naumeri, Malik Asad Munir, Hafiz Mahmood Ahmad, et al.
Computational and Mathematical Methods in Medicine|November 18, 2020
Segmentation of Intensity-Corrupted Medical Images Using Adaptive Weight-Based Hybrid Active ContoursAsif Aziz Memon, Shafiullah Soomro, Muhammad Tanseef Shahid, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Plos One|January 30, 2018
Hybrid two-stage active contour method with region and edge information for intensity inhomogeneous image segmentationShafiullah Soomro, Asad Munir, Kwang Nam Choi
BMC Ophthalmology|February 5, 2024
A systematic review of inherited retinal dystrophies in Pakistan: updates from 1999 to April 2023Asad Munir, Salma Afsar, Atta Ur Rehman
Materials (Basel, Switzerland)|February 11, 2023
Effect of Short-Term Ageing Treatment on Bending Force Behavior of Commercial Nickel-Titanium ArchwireAsad Munir, Muhammad Fauzinizam Razali, Muhammad Hafiz Hassan, et al.
Annals of Medicine|March 3, 2025
Exome sequencing identifies a homozygous splice site variant in <i>RP1</i> as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani familyAbdur Rashid, Asad Munir, Muhammad Zahid, et al.
Computational and Mathematical Methods in Medicine|September 21, 2017
Segmentation of Left and Right Ventricles in Cardiac MRI Using Active ContoursShafiullah Soomro, Farhan Akram, Asad Munir, et al.
Cureus|February 16, 2026
Negative Appendectomy Rates and Their Correlation With the Use of Histopathology: A Clinical AuditJamshid Khan, Yasir Hakim, Aalia Amjad, et al.
Cureus|March 23, 2021
Comparison of Urethrocutaneous Fistula Rate After Single Dartos and Double Dartos Tubularized Incised Plate Urethroplasty in Pediatric HypospadiasFatima Naumeri, Malik Asad Munir, Hafiz Mahmood Ahmad, et al.
Computational and Mathematical Methods in Medicine|November 18, 2020
Segmentation of Intensity-Corrupted Medical Images Using Adaptive Weight-Based Hybrid Active ContoursAsif Aziz Memon, Shafiullah Soomro, Muhammad Tanseef Shahid, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Pageof 2