Search research articles
Contact Us
Filters
Showing results (31-40 of 94) with videos related to
Page
of 10
Sort By:
The Journal of Pediatrics
|
July 25, 2006
Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentials
Daniela Pohl, Kevin Rostasy, Stephanie Treiber-Held, et al.
Genes
|
May 28, 2022
The Benefit of Multigene Panel Testing for the Diagnosis and Management of the Genetic Epilepsies
Heather Leduc-Pessah, Alexandre White-Brown, Taila Hartley, et al.
Multiple Sclerosis and Related Disorders
|
April 30, 2021
Can serum glial fibrillary acidic protein (GFAP) solve the longstanding problem of diagnosis and monitoring progressive multiple sclerosis
Kira Groen, Jeannette Lechner-Scott, Daniela Pohl, et al.
Neurology and Therapy
|
February 16, 2020
Correction to: Long-Term Effect of Immediate Versus Delayed Fingolimod Treatment in Young Adult Patients with Relapsing-Remitting Multiple Sclerosis: Pooled Analysis from the FREEDOMS/FREEDOMSII Trials
Angelo Ghezzi, Tanuja Chitnis, Annik K-Laflamme, et al.
Neurology and Therapy
|
July 21, 2019
Long-Term Effect of Immediate Versus Delayed Fingolimod Treatment in Young Adult Patients with Relapsing-Remitting Multiple Sclerosis: Pooled Analysis from the FREEDOMS/FREEDOMS II Trials
Angelo Ghezzi, Tanuja Chitnis, Annik K-Laflamme, et al.
Journal of Neurology
|
August 29, 2009
Intrathecal antibody production against Epstein-Barr and other neurotropic viruses in pediatric and adult onset multiple sclerosis
Daniela Pohl, Kevin Rostasy, Christian Jacobi, et al.
Journal of Genetic Counseling
|
February 3, 2026
The personal utility of genetic testing in children with epilepsy
Sneha Gupta, Heather Leduc-Pessah, Nick Barrowman, et al.
BMC Medical Genetics
|
February 29, 2016
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
Stephanie M Luco, Daniela Pohl, Erick Sell, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
April 30, 2019
Continuous Electroencephalography Monitoring for Critically Ill Neonates: A Canadian Perspective
Sarah Grace Buttle, Erick Sell, Richard Webster, et al.
Multiple Sclerosis and Related Disorders
|
May 29, 2021
Melatonin and multiple sclerosis
Christopher H Hawkes, Mark D Baker, Daniela Pohl, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 94) with videos related to
Sort By:
Page
of 10
The Journal of Pediatrics
|
July 25, 2006
Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentials
Daniela Pohl, Kevin Rostasy, Stephanie Treiber-Held, et al.
Genes
|
May 28, 2022
The Benefit of Multigene Panel Testing for the Diagnosis and Management of the Genetic Epilepsies
Heather Leduc-Pessah, Alexandre White-Brown, Taila Hartley, et al.
Multiple Sclerosis and Related Disorders
|
April 30, 2021
Can serum glial fibrillary acidic protein (GFAP) solve the longstanding problem of diagnosis and monitoring progressive multiple sclerosis
Kira Groen, Jeannette Lechner-Scott, Daniela Pohl, et al.
Neurology and Therapy
|
February 16, 2020
Correction to: Long-Term Effect of Immediate Versus Delayed Fingolimod Treatment in Young Adult Patients with Relapsing-Remitting Multiple Sclerosis: Pooled Analysis from the FREEDOMS/FREEDOMSII Trials
Angelo Ghezzi, Tanuja Chitnis, Annik K-Laflamme, et al.
Neurology and Therapy
|
July 21, 2019
Long-Term Effect of Immediate Versus Delayed Fingolimod Treatment in Young Adult Patients with Relapsing-Remitting Multiple Sclerosis: Pooled Analysis from the FREEDOMS/FREEDOMS II Trials
Angelo Ghezzi, Tanuja Chitnis, Annik K-Laflamme, et al.
Journal of Neurology
|
August 29, 2009
Intrathecal antibody production against Epstein-Barr and other neurotropic viruses in pediatric and adult onset multiple sclerosis
Daniela Pohl, Kevin Rostasy, Christian Jacobi, et al.
Journal of Genetic Counseling
|
February 3, 2026
The personal utility of genetic testing in children with epilepsy
Sneha Gupta, Heather Leduc-Pessah, Nick Barrowman, et al.
BMC Medical Genetics
|
February 29, 2016
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
Stephanie M Luco, Daniela Pohl, Erick Sell, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
April 30, 2019
Continuous Electroencephalography Monitoring for Critically Ill Neonates: A Canadian Perspective
Sarah Grace Buttle, Erick Sell, Richard Webster, et al.
Multiple Sclerosis and Related Disorders
|
May 29, 2021
Melatonin and multiple sclerosis
Christopher H Hawkes, Mark D Baker, Daniela Pohl, et al.
Page
of 10