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Kristina Martens

Showing results (1-10 of 19) with videos related to

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Multiple Sclerosis and Related Disorders|September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosisMehul Gupta, Kristina Martens, Luanne M Metz, et al.
Frontiers in Neurology|January 28, 2021
Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue TypesKristina Martens, Jamie Leckie, Daniel Fok, et al.
Frontiers in Neurology|November 24, 2018
GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle AtrophyTyler Soule, Cecile Phan, Chris White, et al.
Neuromuscular Disorders : NMD|July 19, 2022
Transcriptome analysis from muscle biopsy tissues in late-onset myopathies identifies potential biomarkers correlating to muscle pathologyMatthew M Joel, Carly Pontifex, Kristina Martens, et al.
Frontiers in Neurology|June 11, 2019
Colchicine Myopathy: A Case Series Including Muscle MRI and <i>ABCB1</i> Polymorphism DataMehul Gupta, Ana Nikolic, Denise Ng, et al.
Journal of Neurogenetics|February 13, 2019
High diagnostic yield and novel variants in very late-onset spasticityMomen Almomen, Kristina Martens, Asfia Quadir, et al.
Circulation. Arrhythmia and Electrophysiology|January 15, 2019
Genetic Association Study in Multigenerational Kindreds With Vasovagal Syncope: Evidence for Involvement of Sex-Specific Serotonin SignalingRobert Sheldon, M Sarah Rose, Debbie Ritchie, et al.
Radiation Oncology (London, England)|July 5, 2013
The prognostic value of tumor necrosis in patients undergoing stereotactic radiosurgery of brain metastasesKristina Martens, Thekla Meyners, Dirk Rades, et al.
Frontiers in Neurology|January 16, 2023
Expression of risk genes linked to vitamin D receptor super-enhancer regions and their association with phenotype severity in multiple sclerosisSarah M Orton, Amarpreet Sangha, Mehul Gupta, et al.
Circulation. Cardiovascular Genetics|July 12, 2012
Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutationsFlorian Kirchner, Anja Schuetz, Leif-Hendrik Boldt, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Multiple Sclerosis and Related Disorders|September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosisMehul Gupta, Kristina Martens, Luanne M Metz, et al.
Frontiers in Neurology|January 28, 2021
Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue TypesKristina Martens, Jamie Leckie, Daniel Fok, et al.
Frontiers in Neurology|November 24, 2018
GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle AtrophyTyler Soule, Cecile Phan, Chris White, et al.
Neuromuscular Disorders : NMD|July 19, 2022
Transcriptome analysis from muscle biopsy tissues in late-onset myopathies identifies potential biomarkers correlating to muscle pathologyMatthew M Joel, Carly Pontifex, Kristina Martens, et al.
Frontiers in Neurology|June 11, 2019
Colchicine Myopathy: A Case Series Including Muscle MRI and <i>ABCB1</i> Polymorphism DataMehul Gupta, Ana Nikolic, Denise Ng, et al.
Journal of Neurogenetics|February 13, 2019
High diagnostic yield and novel variants in very late-onset spasticityMomen Almomen, Kristina Martens, Asfia Quadir, et al.
Circulation. Arrhythmia and Electrophysiology|January 15, 2019
Genetic Association Study in Multigenerational Kindreds With Vasovagal Syncope: Evidence for Involvement of Sex-Specific Serotonin SignalingRobert Sheldon, M Sarah Rose, Debbie Ritchie, et al.
Radiation Oncology (London, England)|July 5, 2013
The prognostic value of tumor necrosis in patients undergoing stereotactic radiosurgery of brain metastasesKristina Martens, Thekla Meyners, Dirk Rades, et al.
Frontiers in Neurology|January 16, 2023
Expression of risk genes linked to vitamin D receptor super-enhancer regions and their association with phenotype severity in multiple sclerosisSarah M Orton, Amarpreet Sangha, Mehul Gupta, et al.
Circulation. Cardiovascular Genetics|July 12, 2012
Molecular insights into arrhythmogenic right ventricular cardiomyopathy caused by plakophilin-2 missense mutationsFlorian Kirchner, Anja Schuetz, Leif-Hendrik Boldt, et al.
Pageof 2