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Clinical Trials (London, England)
|
July 3, 2013
The epilepsy phenome/genome project
, Bassel Abou-Khalil, Brian Alldredge, et al.
Cell
|
June 15, 2026
The critical role of the endogenous immune compartment after CAR T cell therapy in recurrent GBM
Nelson F Freeburg, Daniel Chafamo, Gayathri Konanur Gopikrishna, et al.
Research Square
|
October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
David Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome
Kimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M Nodelman, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Nature
|
August 13, 2013
De novo mutations in epileptic encephalopathies
, , Andrew S Allen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2019
PEDIA: prioritization of exome data by image analysis
Tzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
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of 4
Search research articles
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Showing results (31-40 of 37) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 37 results.
Clinical Trials (London, England)
|
July 3, 2013
The epilepsy phenome/genome project
, Bassel Abou-Khalil, Brian Alldredge, et al.
Cell
|
June 15, 2026
The critical role of the endogenous immune compartment after CAR T cell therapy in recurrent GBM
Nelson F Freeburg, Daniel Chafamo, Gayathri Konanur Gopikrishna, et al.
Research Square
|
October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition
David Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome
Kimberley Jade Anderson, Eirny Tholl Thorolfsdottir, Ilana M Nodelman, et al.
Brain : a Journal of Neurology
|
April 6, 2017
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, et al.
Nature
|
August 13, 2013
De novo mutations in epileptic encephalopathies
, , Andrew S Allen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 6, 2019
PEDIA: prioritization of exome data by image analysis
Tzung-Chien Hsieh, Martin A Mensah, Jean T Pantel, et al.
Page
of 4