Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Mozaffar

Showing results (11-20 of 25) with videos related to

Pageof 3
Sort By:
Journal of Neurology|September 25, 1998
Clinical correlates of granulomas in muscleT Mozaffar, G Lopate, A Pestronk
JPMA. the Journal of the Pakistan Medical Association|December 29, 2000
Gram negative meningitis resulting from rupture of a spinal epidural abscess into the subarachnoid spaceS Lodhi, T Mozaffar, A R Sarwari
Neurology|April 1, 1998
Paraneoplastic necrotizing myopathy: clinical and pathological featuresM I Levin, T Mozaffar, M T Al-Lozi, et al.
JPMA. the Journal of the Pakistan Medical Association|June 20, 2002
Predictors of mortality in brain abscessH U Qureshi, A A Habib, A A Siddiqui, et al.
Neuroscience|March 7, 2015
Activation of the Wnt/β-catenin signaling cascade after traumatic nerve injuryS Kurimoto, J Jung, M Tapadia, et al.
Cell Death & Disease|August 18, 2012
Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in miceH Z Yin, A Nalbandian, C-I Hsu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2015
Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvementN A Goyal, T M Cash, U Alam, et al.
Clinical Genetics|July 11, 2017
Genotype-phenotype study in patients with valosin-containing protein mutations associated with multisystem proteinopathyE Al-Obeidi, S Al-Tahan, A Surampalli, et al.
JPMA. the Journal of the Pakistan Medical Association|February 10, 2004
Ischemic stroke subtypes in Pakistan: the Aga Khan University Stroke Data BankN A Syed, B A Khealani, S Ali, et al.
Clinical Genetics|December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Journal of Neurology|September 25, 1998
Clinical correlates of granulomas in muscleT Mozaffar, G Lopate, A Pestronk
JPMA. the Journal of the Pakistan Medical Association|December 29, 2000
Gram negative meningitis resulting from rupture of a spinal epidural abscess into the subarachnoid spaceS Lodhi, T Mozaffar, A R Sarwari
Neurology|April 1, 1998
Paraneoplastic necrotizing myopathy: clinical and pathological featuresM I Levin, T Mozaffar, M T Al-Lozi, et al.
JPMA. the Journal of the Pakistan Medical Association|June 20, 2002
Predictors of mortality in brain abscessH U Qureshi, A A Habib, A A Siddiqui, et al.
Neuroscience|March 7, 2015
Activation of the Wnt/β-catenin signaling cascade after traumatic nerve injuryS Kurimoto, J Jung, M Tapadia, et al.
Cell Death & Disease|August 18, 2012
Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in miceH Z Yin, A Nalbandian, C-I Hsu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 11, 2015
Seropositivity for NT5c1A antibody in sporadic inclusion body myositis predicts more severe motor, bulbar and respiratory involvementN A Goyal, T M Cash, U Alam, et al.
Clinical Genetics|July 11, 2017
Genotype-phenotype study in patients with valosin-containing protein mutations associated with multisystem proteinopathyE Al-Obeidi, S Al-Tahan, A Surampalli, et al.
JPMA. the Journal of the Pakistan Medical Association|February 10, 2004
Ischemic stroke subtypes in Pakistan: the Aga Khan University Stroke Data BankN A Syed, B A Khealani, S Ali, et al.
Clinical Genetics|December 24, 2010
Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNER A Maselli, J Arredondo, O Cagney, et al.
Pageof 3