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Neurology
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May 26, 2021
Association of <i>SLC32A1</i> Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
Sarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
Epilepsia
|
March 17, 2022
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
Ciarán Campbell, Mark McCormack, Sonn Patel, et al.
Epilepsia
|
March 16, 2024
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Robert J Carton, Michael G Doyle, Hugh Kearney, et al.
Human Molecular Genetics
|
February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions
Timothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approach
Anna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
American Journal of Human Genetics
|
September 11, 2012
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
M Chiara Manzini, Dimira E Tambunan, R Sean Hill, et al.
Experimental Hematology & Oncology
|
June 23, 2025
Mitotic MTH1 inhibitor karonudib kills epithelial ovarian cancer independent of platinum sensitivity
Rachel M Hurley, Jill M Wagner, Arun Kanakkanthara, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 1, 2026
PET/CT-Guided Management of Immune Checkpoint Blockade and Post-Treatment Multi-Modal Profiling in Long-Term Responders with Metastatic Lung Cancer in the National Network Genomic Medicine Lung Cancer Germany (nNGM)
N Frost, M Joosten, J Franzen, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Clinical Lung Cancer
|
August 17, 2024
Multicenter Real-World Analysis of Combined MET and EGFR Inhibition in Patients With Non-Small Cell Lung Cancer and Acquired MET Amplification or Polysomy After EGFR Inhibition
Fabian Acker, Alexandra Klein, Anna Rasokat, et al.
Page
of 40
Search research articles
Search
Showing results (351-360 of 393) with videos related to
Sort By:
Page
of 40
Neurology
|
May 26, 2021
Association of <i>SLC32A1</i> Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
Sarah E Heron, Brigid M Regan, Rebekah V Harris, et al.
Epilepsia
|
March 17, 2022
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
Ciarán Campbell, Mark McCormack, Sonn Patel, et al.
Epilepsia
|
March 16, 2024
Somatic variants as a cause of drug-resistant epilepsy including mesial temporal lobe epilepsy with hippocampal sclerosis
Robert J Carton, Michael G Doyle, Hugh Kearney, et al.
Human Molecular Genetics
|
February 9, 2022
Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions
Timothy E Green, Joshua E Motelow, Mark F Bennett, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
June 3, 2019
New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approach
Anna Alkelai, Lior Greenbaum, Erin L Heinzen, et al.
American Journal of Human Genetics
|
September 11, 2012
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome
M Chiara Manzini, Dimira E Tambunan, R Sean Hill, et al.
Experimental Hematology & Oncology
|
June 23, 2025
Mitotic MTH1 inhibitor karonudib kills epithelial ovarian cancer independent of platinum sensitivity
Rachel M Hurley, Jill M Wagner, Arun Kanakkanthara, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
January 1, 2026
PET/CT-Guided Management of Immune Checkpoint Blockade and Post-Treatment Multi-Modal Profiling in Long-Term Responders with Metastatic Lung Cancer in the National Network Genomic Medicine Lung Cancer Germany (nNGM)
N Frost, M Joosten, J Franzen, et al.
European Journal of Human Genetics : EJHG
|
December 14, 2023
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene
Eleni Panagiotakaki, Francesco D Tiziano, Mohamad A Mikati, et al.
Clinical Lung Cancer
|
August 17, 2024
Multicenter Real-World Analysis of Combined MET and EGFR Inhibition in Patients With Non-Small Cell Lung Cancer and Acquired MET Amplification or Polysomy After EGFR Inhibition
Fabian Acker, Alexandra Klein, Anna Rasokat, et al.
Page
of 40