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Annals of Neurology
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April 16, 2023
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties
Maria Cristina Cioclu, Ilaria Mosca, Paolo Ambrosino, et al.
Neuropediatrics
|
November 19, 2025
Crisis-like Seizure Exacerbations in NPRL3-related Epilepsy: Phenotypic Features and Treatment Outcomes
V Thormeyer, Z Meyer, T Polster, et al.
The Review of Scientific Instruments
|
February 11, 2024
Robust unfolding of MeV x-ray spectra from filter stack spectrometer data
C-S Wong, J Strehlow, D P Broughton, et al.
Reviews in Fish Biology and Fisheries
|
June 26, 2023
Global responses to the COVID-19 pandemic by recreational anglers: considerations for developing more resilient and sustainable fisheries
J Robert Britton, Adrian C Pinder, Josep Alós, et al.
Nucleic Acids Research
|
February 27, 2004
ARB: a software environment for sequence data
Wolfgang Ludwig, Oliver Strunk, Ralf Westram, et al.
Brain : a Journal of Neurology
|
December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotype
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine
|
May 23, 2024
2023 Society for Academic Emergency Medicine Consensus Conference on Precision Emergency Medicine: Development of a policy-relevant, patient-centered research agenda
Matthew Strehlow, Michael A Gisondi, Holly Caretta-Weyer, et al.
BMJ Open
|
May 8, 2023
Observational study of organisational responses of 17 US hospitals over the first year of the COVID-19 pandemic
Esther K Choo, Matthew Strehlow, Marina Del Rios, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Molecular Psychiatry
|
October 14, 2025
GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
Johannes R Lemke, Andrea Eoli, Ilona Krey, et al.
Page
of 27
Search research articles
Search
Showing results (251-260 of 268) with videos related to
Sort By:
Page
of 27
Annals of Neurology
|
April 16, 2023
KCNT2-Related Disorders: Phenotypes, Functional, and Pharmacological Properties
Maria Cristina Cioclu, Ilaria Mosca, Paolo Ambrosino, et al.
Neuropediatrics
|
November 19, 2025
Crisis-like Seizure Exacerbations in NPRL3-related Epilepsy: Phenotypic Features and Treatment Outcomes
V Thormeyer, Z Meyer, T Polster, et al.
The Review of Scientific Instruments
|
February 11, 2024
Robust unfolding of MeV x-ray spectra from filter stack spectrometer data
C-S Wong, J Strehlow, D P Broughton, et al.
Reviews in Fish Biology and Fisheries
|
June 26, 2023
Global responses to the COVID-19 pandemic by recreational anglers: considerations for developing more resilient and sustainable fisheries
J Robert Britton, Adrian C Pinder, Josep Alós, et al.
Nucleic Acids Research
|
February 27, 2004
ARB: a software environment for sequence data
Wolfgang Ludwig, Oliver Strunk, Ralf Westram, et al.
Brain : a Journal of Neurology
|
December 14, 2018
GRIN2A-related disorders: genotype and functional consequence predict phenotype
Vincent Strehlow, Henrike O Heyne, Danique R M Vlaskamp, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine
|
May 23, 2024
2023 Society for Academic Emergency Medicine Consensus Conference on Precision Emergency Medicine: Development of a policy-relevant, patient-centered research agenda
Matthew Strehlow, Michael A Gisondi, Holly Caretta-Weyer, et al.
BMJ Open
|
May 8, 2023
Observational study of organisational responses of 17 US hospitals over the first year of the COVID-19 pandemic
Esther K Choo, Matthew Strehlow, Marina Del Rios, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Molecular Psychiatry
|
October 14, 2025
GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
Johannes R Lemke, Andrea Eoli, Ilona Krey, et al.
Page
of 27