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Multiple Sclerosis and Related Disorders
|
September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosis
Mehul 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 Types
Kristina Martens, Jamie Leckie, Daniel Fok, et al.
Frontiers in Neurology
|
November 24, 2018
GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle Atrophy
Tyler 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 pathology
Matthew 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 Data
Mehul Gupta, Ana Nikolic, Denise Ng, et al.
Journal of Neurogenetics
|
February 13, 2019
High diagnostic yield and novel variants in very late-onset spasticity
Momen 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 Signaling
Robert 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 metastases
Kristina 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 sclerosis
Sarah 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 mutations
Florian Kirchner, Anja Schuetz, Leif-Hendrik Boldt, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Multiple Sclerosis and Related Disorders
|
September 29, 2019
Long noncoding RNAs associated with phenotypic severity in multiple sclerosis
Mehul 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 Types
Kristina Martens, Jamie Leckie, Daniel Fok, et al.
Frontiers in Neurology
|
November 24, 2018
GNE Myopathy With Novel Mutations and Pronounced Paraspinal Muscle Atrophy
Tyler 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 pathology
Matthew 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 Data
Mehul Gupta, Ana Nikolic, Denise Ng, et al.
Journal of Neurogenetics
|
February 13, 2019
High diagnostic yield and novel variants in very late-onset spasticity
Momen 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 Signaling
Robert 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 metastases
Kristina 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 sclerosis
Sarah 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 mutations
Florian Kirchner, Anja Schuetz, Leif-Hendrik Boldt, et al.
Page
of 2