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Payam Soltanzadeh

Showing results (1-10 of 11) with videos related to

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Genes|February 25, 2022
Myotonic Dystrophies: A Genetic OverviewPayam Soltanzadeh
The Laryngoscope|July 1, 2024
Heterogeneous Presentations and Serologies in Myasthenia Gravis Patients Presenting with DysphagiaClare Moffatt, Pranati Pillutla, Payam Soltanzadeh, et al.
Journal of the Neurological Sciences|June 2, 2017
Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case seriesYuebing Li, Jason Valent, Payam Soltanzadeh, et al.
European Neurology|December 21, 2006
Wilson's disease: a great masqueraderAkbar Soltanzadeh, Payam Soltanzadeh, Shahriar Nafissi, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 21, 2017
Intravascular T-cell lymphoma: A rare, poorly characterized entity with cytotoxic phenotypeTara L Sharma, Gabrielle A Yeaney, Payam Soltanzadeh, et al.
Cell Biology International|November 27, 2019
In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membraneFatemeh Ghanavatinejad, Zahra Pourteymourfard-Tabrizi, Karim Mahnam, et al.
Plos One|January 18, 2013
A mutation causes MuSK reduced sensitivity to agrin and congenital myastheniaAsma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, et al.
The New England Journal of Medicine|February 18, 2026
An Antibody-Oligonucleotide Conjugate for Myotonic Dystrophy Type 1Nicholas E Johnson, Li-Jung Tai, Johanna I Hamel, et al.
Human Mutation|October 6, 2011
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD geneKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Neuromuscular Disorders : NMD|July 16, 2010
Clinical and genetic characterization of manifesting carriers of DMD mutationsPayam Soltanzadeh, Michael J Friez, Diane Dunn, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Genes|February 25, 2022
Myotonic Dystrophies: A Genetic OverviewPayam Soltanzadeh
The Laryngoscope|July 1, 2024
Heterogeneous Presentations and Serologies in Myasthenia Gravis Patients Presenting with DysphagiaClare Moffatt, Pranati Pillutla, Payam Soltanzadeh, et al.
Journal of the Neurological Sciences|June 2, 2017
Diagnostic challenges in POEMS syndrome presenting with polyneuropathy: A case seriesYuebing Li, Jason Valent, Payam Soltanzadeh, et al.
European Neurology|December 21, 2006
Wilson's disease: a great masqueraderAkbar Soltanzadeh, Payam Soltanzadeh, Shahriar Nafissi, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 21, 2017
Intravascular T-cell lymphoma: A rare, poorly characterized entity with cytotoxic phenotypeTara L Sharma, Gabrielle A Yeaney, Payam Soltanzadeh, et al.
Cell Biology International|November 27, 2019
In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membraneFatemeh Ghanavatinejad, Zahra Pourteymourfard-Tabrizi, Karim Mahnam, et al.
Plos One|January 18, 2013
A mutation causes MuSK reduced sensitivity to agrin and congenital myastheniaAsma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, et al.
The New England Journal of Medicine|February 18, 2026
An Antibody-Oligonucleotide Conjugate for Myotonic Dystrophy Type 1Nicholas E Johnson, Li-Jung Tai, Johanna I Hamel, et al.
Human Mutation|October 6, 2011
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD geneKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.
Neuromuscular Disorders : NMD|July 16, 2010
Clinical and genetic characterization of manifesting carriers of DMD mutationsPayam Soltanzadeh, Michael J Friez, Diane Dunn, et al.
Pageof 2