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Jahannaz Dastgir

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Journal of Child Neurology|February 5, 2009
Acute tumefactive demyelinating lesions in a pediatric patient with known diagnosis of multiple sclerosis: review of the literature and treatment proposalJahannaz Dastgir, Francis J DiMario
Pediatric Radiology|June 22, 2016
Imaging findings in a child with calcineurin inhibitor-induced pain syndrome after bone marrow transplant for beta thalassemia majorRama S Ayyala, Staci D Arnold, Monica Bhatia, et al.
Muscle & Nerve|July 17, 2015
Electrical impedance myography discriminates congenital muscular dystrophy from controlsDaniel P Schwartz, Jahannaz Dastgir, Anam Salman, et al.
Muscle & Nerve|November 29, 2014
Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order AmishJonathan D Marra, Kristin E Engelstad, Arunkanth Ankala, et al.
JIMD Reports|July 21, 2020
Treatment of infantile neuroaxonal dystrophy with RT001: A di-deuterated ethyl ester of linoleic acid: Report of two casesDarius Adams, Mark Midei, Jahannaz Dastgir, et al.
Neuromuscular Disorders : NMD|August 22, 2020
Cardiac MRI identifies valvular and myocardial disease in a subset of ANO5-related muscular dystrophy patientsRanjini Srinivasan, Pomi Yun, Sarah Neuhaus, et al.
Neurology|March 15, 2015
Intrafamilial variability in GMPPB-associated dystroglycanopathy: Broadening of the phenotypeDiana X Bharucha-Goebel, Erin Neil, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD|September 28, 2013
'Double trouble': diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasiaSandra Donkervoort, Alice Schindler, Carolina Tesi-Rocha, et al.
Annals of Clinical and Translational Neurology|November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsiesEleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Journal of Neuromuscular Diseases|September 10, 2019
Identification of a Novel Deep Intronic Mutation in CAPN3 Presenting a Promising Target for Therapeutic Splice ModulationYing Hu, Payam Mohassel, Sandra Donkervoort, et al.
Pageof 3

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

Sort By:
Pageof 3
Journal of Child Neurology|February 5, 2009
Acute tumefactive demyelinating lesions in a pediatric patient with known diagnosis of multiple sclerosis: review of the literature and treatment proposalJahannaz Dastgir, Francis J DiMario
Pediatric Radiology|June 22, 2016
Imaging findings in a child with calcineurin inhibitor-induced pain syndrome after bone marrow transplant for beta thalassemia majorRama S Ayyala, Staci D Arnold, Monica Bhatia, et al.
Muscle & Nerve|July 17, 2015
Electrical impedance myography discriminates congenital muscular dystrophy from controlsDaniel P Schwartz, Jahannaz Dastgir, Anam Salman, et al.
Muscle & Nerve|November 29, 2014
Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order AmishJonathan D Marra, Kristin E Engelstad, Arunkanth Ankala, et al.
JIMD Reports|July 21, 2020
Treatment of infantile neuroaxonal dystrophy with RT001: A di-deuterated ethyl ester of linoleic acid: Report of two casesDarius Adams, Mark Midei, Jahannaz Dastgir, et al.
Neuromuscular Disorders : NMD|August 22, 2020
Cardiac MRI identifies valvular and myocardial disease in a subset of ANO5-related muscular dystrophy patientsRanjini Srinivasan, Pomi Yun, Sarah Neuhaus, et al.
Neurology|March 15, 2015
Intrafamilial variability in GMPPB-associated dystroglycanopathy: Broadening of the phenotypeDiana X Bharucha-Goebel, Erin Neil, Sandra Donkervoort, et al.
Neuromuscular Disorders : NMD|September 28, 2013
'Double trouble': diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasiaSandra Donkervoort, Alice Schindler, Carolina Tesi-Rocha, et al.
Annals of Clinical and Translational Neurology|November 3, 2021
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsiesEleonora Guadagnin, Payam Mohassel, Kory R Johnson, et al.
Journal of Neuromuscular Diseases|September 10, 2019
Identification of a Novel Deep Intronic Mutation in CAPN3 Presenting a Promising Target for Therapeutic Splice ModulationYing Hu, Payam Mohassel, Sandra Donkervoort, et al.
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