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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 18, 2021
Vaccination and childhood epilepsies
Dana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Anticancer Research
|
September 9, 2018
Differential Mechanism of Action of 3,4',7-O-trimethylquercetin in Three Types of Ovarian Cancer Cells
A H M Zuberi Ashraf, Syeda H Afroze, Kosei Yamauchi, et al.
Epilepsia
|
June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk
Kenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2024
Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study
Erin Freeman-Jones, Galia Wilson, Claire Eldred, et al.
Mbio
|
August 6, 2024
One-step genome engineering in bee gut bacterial symbionts
Patrick J Lariviere, A H M Zuberi Ashraf, Lucio Navarro-Escalante, et al.
Indian Journal of Cancer
|
February 25, 2016
Simple multiplex RT-PCR for identifying common fusion BCR-ABL transcript types and evaluation of molecular response of the a2b2 and a2b3 transcripts to Imatinib resistance in north Indian chronic myeloid leukemia patients
Rashid Mir, I Ahmad, J Javid, et al.
Epilepsy & Behavior : E&B
|
March 25, 2022
The clinical, economic, and humanistic burden of Dravet syndrome - A systematic literature review
Joseph Sullivan, Alison M Deighton, Maria Candida Vila, et al.
Brain & Development
|
January 26, 2005
The movement disorders of Coffin-Lowry syndrome
John B P Stephenson, Mary C Hoffman, Aline J C Russell, et al.
Journal of Medical Genetics
|
July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Sarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.
Brain : a Journal of Neurology
|
January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapy
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
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of 17
Search research articles
Search
Showing results (91-100 of 170) with videos related to
Sort By:
Page
of 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 18, 2021
Vaccination and childhood epilepsies
Dana Craiu, Zvonka Rener Primec, Lieven Lagae, et al.
Anticancer Research
|
September 9, 2018
Differential Mechanism of Action of 3,4',7-O-trimethylquercetin in Three Types of Ovarian Cancer Cells
A H M Zuberi Ashraf, Syeda H Afroze, Kosei Yamauchi, et al.
Epilepsia
|
June 7, 2018
Heart rate variability in epilepsy: A potential biomarker of sudden unexpected death in epilepsy risk
Kenneth A Myers, Luis E Bello-Espinosa, Joseph D Symonds, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2024
Caregiver burden and therapeutic needs in Dravet syndrome - A national UK cross-sectional questionnaire study
Erin Freeman-Jones, Galia Wilson, Claire Eldred, et al.
Mbio
|
August 6, 2024
One-step genome engineering in bee gut bacterial symbionts
Patrick J Lariviere, A H M Zuberi Ashraf, Lucio Navarro-Escalante, et al.
Indian Journal of Cancer
|
February 25, 2016
Simple multiplex RT-PCR for identifying common fusion BCR-ABL transcript types and evaluation of molecular response of the a2b2 and a2b3 transcripts to Imatinib resistance in north Indian chronic myeloid leukemia patients
Rashid Mir, I Ahmad, J Javid, et al.
Epilepsy & Behavior : E&B
|
March 25, 2022
The clinical, economic, and humanistic burden of Dravet syndrome - A systematic literature review
Joseph Sullivan, Alison M Deighton, Maria Candida Vila, et al.
Brain & Development
|
January 26, 2005
The movement disorders of Coffin-Lowry syndrome
John B P Stephenson, Mary C Hoffman, Aline J C Russell, et al.
Journal of Medical Genetics
|
July 11, 2009
De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin
Sarah E Heron, Ingrid E Scheffer, Xenia Iona, et al.
Brain : a Journal of Neurology
|
January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapy
Andreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Page
of 17