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Shahnaz Ibrahim

Showing results (1-10 of 30) with videos related to

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Journal of Ayub Medical College, Abbottabad : JAMC|September 19, 2006
Acute transverse myelitis in childrenSyed Asif Masood, Shahnaz Ibrahim
Journal of Child Neurology|January 13, 2025
Unveiling Pediatric Neurosarcoidosis Mimicking Central Nervous System Tuberculosis: Diagnostic ChallengesMohammad Raza, Isbaah Tejani, Shahnaz Ibrahim
Brain & Development|July 17, 2009
Missed opportunities in surveillance and screening systems to detect developmental delay: A developing country perspectiveZarmeneh Aly, Fawad Taj, Shahnaz Ibrahim
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|March 11, 2024
Clinical Spectrum, Treatment and Outcome of Children with Autoimmune EncephalitisMohammad Raza, Khairunnisa Mukhtiar, Shahnaz Ibrahim
Neurology India|July 25, 2012
Spinal muscular atrophy: clinical spectrum and genetic mutations in Pakistani childrenShahnaz Ibrahim, Tariq Moatter, Ali Faisal Saleem
Brain & Development|April 28, 2016
Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis (HMDPC) due to mutation in the SLC30A10 geneKhairunnisa Mukhtiar, Shahnaz Ibrahim, Karin Tuschl, et al.
BMJ Case Reports|December 16, 2021
Acute retinal necrosis with exudative retinal detachment in a childBenish Aslam Perhiar, Ma Rehman Siddiqui, Shahnaz Ibrahim
Journal of Child Neurology|March 29, 2025
<i>TANGO-2</i>: A Rare Genetic Condition With Severe Clinical Presentation of Encephalopathy, Rhabdomyolysis, and Cardiac Rhythm Disorders in 2 ChildrenKhairunnisa Mukhtiar, Shahnaz Ibrahim, Quart-Ul-Ain Khalid
BMC Pediatrics|January 19, 2010
Clinical profile and treatment of infantile spasms using vigabatrin and ACTH--a developing country perspectiveShahnaz Ibrahim, Shamshad Gulab, Sidra Ishaque, et al.
BMJ Case Reports|July 11, 2024
Atypical presentation of biotinidase deficiency: masquerading neuromyelitis optica spectrum disorderFarhan Ali, Khairunnisa Mukhtiar, Mohammad Raza, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Journal of Ayub Medical College, Abbottabad : JAMC|September 19, 2006
Acute transverse myelitis in childrenSyed Asif Masood, Shahnaz Ibrahim
Journal of Child Neurology|January 13, 2025
Unveiling Pediatric Neurosarcoidosis Mimicking Central Nervous System Tuberculosis: Diagnostic ChallengesMohammad Raza, Isbaah Tejani, Shahnaz Ibrahim
Brain & Development|July 17, 2009
Missed opportunities in surveillance and screening systems to detect developmental delay: A developing country perspectiveZarmeneh Aly, Fawad Taj, Shahnaz Ibrahim
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|March 11, 2024
Clinical Spectrum, Treatment and Outcome of Children with Autoimmune EncephalitisMohammad Raza, Khairunnisa Mukhtiar, Shahnaz Ibrahim
Neurology India|July 25, 2012
Spinal muscular atrophy: clinical spectrum and genetic mutations in Pakistani childrenShahnaz Ibrahim, Tariq Moatter, Ali Faisal Saleem
Brain & Development|April 28, 2016
Hypermanganesemia with Dystonia, Polycythemia and Cirrhosis (HMDPC) due to mutation in the SLC30A10 geneKhairunnisa Mukhtiar, Shahnaz Ibrahim, Karin Tuschl, et al.
BMJ Case Reports|December 16, 2021
Acute retinal necrosis with exudative retinal detachment in a childBenish Aslam Perhiar, Ma Rehman Siddiqui, Shahnaz Ibrahim
Journal of Child Neurology|March 29, 2025
<i>TANGO-2</i>: A Rare Genetic Condition With Severe Clinical Presentation of Encephalopathy, Rhabdomyolysis, and Cardiac Rhythm Disorders in 2 ChildrenKhairunnisa Mukhtiar, Shahnaz Ibrahim, Quart-Ul-Ain Khalid
BMC Pediatrics|January 19, 2010
Clinical profile and treatment of infantile spasms using vigabatrin and ACTH--a developing country perspectiveShahnaz Ibrahim, Shamshad Gulab, Sidra Ishaque, et al.
BMJ Case Reports|July 11, 2024
Atypical presentation of biotinidase deficiency: masquerading neuromyelitis optica spectrum disorderFarhan Ali, Khairunnisa Mukhtiar, Mohammad Raza, et al.
Pageof 3