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Human Molecular Genetics
|
August 1, 1997
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
F V Elmslie, M Rees, M P Williamson, et al.
Epilepsy Research
|
June 7, 2002
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14
Nichole L Taske, Magali P Williamson, Andrew Makoff, et al.
Cancers
|
October 15, 2020
A Novel Orthotopic Patient-Derived Xenograft Model of Radiation-Induced Glioma Following Medulloblastoma
Jacqueline P Whitehouse, Meegan Howlett, Hilary Hii, et al.
Annals of Neurology
|
December 15, 2018
Genotype, extrapyramidal features, and severity of variant ataxia-telangiectasia
Katherine Schon, Nienke J H van Os, Nicholas Oscroft, et al.
Ebiomedicine
|
December 27, 2021
Relationship of admission blood proteomic biomarkers levels to lesion type and lesion burden in traumatic brain injury: A CENTER-TBI study
Daniel P Whitehouse, Miguel Monteiro, Endre Czeiter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 18, 2024
Long term outcome in non-multiple sclerosis paediatric acquired demyelinating syndromes
Evangeline Wassmer, Charly Billaud, Michael Absoud, et al.
Frontiers in Neurology
|
February 7, 2025
Long-term safety of dexamethasone sodium phosphate encapsulated in autologous erythrocytes in pediatric patients with ataxia telangiectasia
Mary Kay Koenig, Vincenzo Leuzzi, Riadh Gouider, et al.
Frontiers in Oncology
|
March 20, 2023
<i>In vivo</i> loss of tumorigenicity in a patient-derived orthotopic xenograft mouse model of ependymoma
Jacqueline P Whitehouse, Hilary Hii, Chelsea Mayoh, et al.
Epilepsia
|
February 7, 2017
Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases
Joseph D Symonds, Shelagh Joss, Kay A Metcalfe, et al.
JMIR Neurotechnology
|
December 4, 2025
Clinical Perspectives on Using Remote Measurement Technology in Assessing Epilepsy, Multiple Sclerosis, and Depression: Delphi Study
Jacob A Andrews, Michael P Craven, Boliang Guo, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Human Molecular Genetics
|
August 1, 1997
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
F V Elmslie, M Rees, M P Williamson, et al.
Epilepsy Research
|
June 7, 2002
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14
Nichole L Taske, Magali P Williamson, Andrew Makoff, et al.
Cancers
|
October 15, 2020
A Novel Orthotopic Patient-Derived Xenograft Model of Radiation-Induced Glioma Following Medulloblastoma
Jacqueline P Whitehouse, Meegan Howlett, Hilary Hii, et al.
Annals of Neurology
|
December 15, 2018
Genotype, extrapyramidal features, and severity of variant ataxia-telangiectasia
Katherine Schon, Nienke J H van Os, Nicholas Oscroft, et al.
Ebiomedicine
|
December 27, 2021
Relationship of admission blood proteomic biomarkers levels to lesion type and lesion burden in traumatic brain injury: A CENTER-TBI study
Daniel P Whitehouse, Miguel Monteiro, Endre Czeiter, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 18, 2024
Long term outcome in non-multiple sclerosis paediatric acquired demyelinating syndromes
Evangeline Wassmer, Charly Billaud, Michael Absoud, et al.
Frontiers in Neurology
|
February 7, 2025
Long-term safety of dexamethasone sodium phosphate encapsulated in autologous erythrocytes in pediatric patients with ataxia telangiectasia
Mary Kay Koenig, Vincenzo Leuzzi, Riadh Gouider, et al.
Frontiers in Oncology
|
March 20, 2023
<i>In vivo</i> loss of tumorigenicity in a patient-derived orthotopic xenograft mouse model of ependymoma
Jacqueline P Whitehouse, Hilary Hii, Chelsea Mayoh, et al.
Epilepsia
|
February 7, 2017
Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases
Joseph D Symonds, Shelagh Joss, Kay A Metcalfe, et al.
JMIR Neurotechnology
|
December 4, 2025
Clinical Perspectives on Using Remote Measurement Technology in Assessing Epilepsy, Multiple Sclerosis, and Depression: Delphi Study
Jacob A Andrews, Michael P Craven, Boliang Guo, et al.
Page
of 14