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Shahnaz Ibrahim

Showing results (11-20 of 30) with videos related to

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Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 8, 2014
Early recovery in post Varicella transverse myelitisPrem Chand, Shahnaz Ibrahim, Syed Sohail Zaidi, et al.
SAGE Open Medical Case Reports|November 29, 2023
Diagnostic dilemmas and challenges in the management of myasthenia in infants and toddlers: A case reportKhairunnisa Mukhtiar, Mohammad Raza, Isbaah Tejani, et al.
Molecular Biology Reports|March 31, 2018
CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani childrenShahnaz Ibrahim, Saadia Maqbool, Maleeha Azam, et al.
Journal of Community Health|August 14, 2014
Perceptions and attitudes of pharmacy students towards volunteering at health promotional programs: a cross-sectional study from MalaysiaFahad Saleem, Mohamed Azmi Hassali, Zehan Shahnaz Ibrahim, et al.
American Journal of Medical Genetics. Part A|June 27, 2023
The spectrum of hereditary neuromuscular disorders in the Pakistani populationFizza Akbar, Shafaq Muhammad Saleem, Ehtesham Khalid, et al.
Epilepsy & Behavior Reports|December 6, 2022
Utility of genetic testing in pediatric epilepsy: Experience from a low to middle-income countryFizza Akbar, Raisa Saleh, Salman Kirmani, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|August 24, 2014
Subacute sclerosing panencephalitis: clinical and demographic characteristicsArshad Rafique, Nida Amjad, Prem Chand, et al.
Genetic Testing and Molecular Biomarkers|June 4, 2019
MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective StudyZeeshan Ansar, Asghar Nasir, Tariq Moatter, et al.
Pediatric Neurology|November 6, 2022
Spectrum of Common Pediatric Neurological Disorders: A Cross-Sectional Study From Three Tertiary Care Centres Across PakistanPrem Chand, Tipu Sultan, Shazia Kulsoom, et al.
Human Genomics|February 12, 2026
Expanding the repertoire of loss-of-function variants in HACE1 causing complex spastic paraplegia: literature review and recommendations on clinical managementHammad Yousaf, Sajid Ali, Ahad Yousuf Moulvi, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|June 8, 2014
Early recovery in post Varicella transverse myelitisPrem Chand, Shahnaz Ibrahim, Syed Sohail Zaidi, et al.
SAGE Open Medical Case Reports|November 29, 2023
Diagnostic dilemmas and challenges in the management of myasthenia in infants and toddlers: A case reportKhairunnisa Mukhtiar, Mohammad Raza, Isbaah Tejani, et al.
Molecular Biology Reports|March 31, 2018
CBS mutations and MTFHR SNPs causative of hyperhomocysteinemia in Pakistani childrenShahnaz Ibrahim, Saadia Maqbool, Maleeha Azam, et al.
Journal of Community Health|August 14, 2014
Perceptions and attitudes of pharmacy students towards volunteering at health promotional programs: a cross-sectional study from MalaysiaFahad Saleem, Mohamed Azmi Hassali, Zehan Shahnaz Ibrahim, et al.
American Journal of Medical Genetics. Part A|June 27, 2023
The spectrum of hereditary neuromuscular disorders in the Pakistani populationFizza Akbar, Shafaq Muhammad Saleem, Ehtesham Khalid, et al.
Epilepsy & Behavior Reports|December 6, 2022
Utility of genetic testing in pediatric epilepsy: Experience from a low to middle-income countryFizza Akbar, Raisa Saleh, Salman Kirmani, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|August 24, 2014
Subacute sclerosing panencephalitis: clinical and demographic characteristicsArshad Rafique, Nida Amjad, Prem Chand, et al.
Genetic Testing and Molecular Biomarkers|June 4, 2019
MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective StudyZeeshan Ansar, Asghar Nasir, Tariq Moatter, et al.
Pediatric Neurology|November 6, 2022
Spectrum of Common Pediatric Neurological Disorders: A Cross-Sectional Study From Three Tertiary Care Centres Across PakistanPrem Chand, Tipu Sultan, Shazia Kulsoom, et al.
Human Genomics|February 12, 2026
Expanding the repertoire of loss-of-function variants in HACE1 causing complex spastic paraplegia: literature review and recommendations on clinical managementHammad Yousaf, Sajid Ali, Ahad Yousuf Moulvi, et al.
Pageof 3