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Neuroimage
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November 9, 2022
CerebNet: A fast and reliable deep-learning pipeline for detailed cerebellum sub-segmentation
Jennifer Faber, David Kügler, Emad Bahrami, et al.
Nature Medicine
|
April 15, 2020
Adaptive evolution of virulence and persistence in carbapenem-resistant Klebsiella pneumoniae
Christoph M Ernst, Julian R Braxton, Carlos A Rodriguez-Osorio, et al.
Journal of Neurodevelopmental Disorders
|
December 16, 2022
Long-term follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder: corpus callosum white matter microstructure and neurocognitive outcomes
Blake A Gimbel, Mary E Anthony, Abigail M Ernst, et al.
Forensic Science International
|
March 12, 2004
Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts
G Tully, S M Barritt, K Bender, et al.
The Journal of Pediatrics
|
August 28, 2023
Differences in Quality of Life in Children Across the Spectrum of Congenital Heart Disease
Amy M O'Connor, Amy Cassedy, Jo Wray, et al.
Annals of Clinical Biochemistry
|
July 11, 2006
Predictors of elevated cardiac troponin T on admission in ST-segment elevation myocardial infarction
Saman Rasoul, Mark B Nienhuis, Jan Paul Ottervanger, et al.
Journal of Pediatric Psychology
|
July 22, 2025
Stigma in differences of sex development: a scoping review
Canice E Crerand, Kristina I Suorsa-Johnson, Michelle M Ernst, et al.
Nature Reviews. Clinical Oncology
|
March 15, 2025
Utilizing ctDNA to discover mechanisms of resistance to targeted therapies in patients with metastatic NSCLC: towards more informative trials
Sophie M Ernst, Mihaela Aldea, Jan H von der Thüsen, et al.
American Journal of Human Genetics
|
October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
M A Simpson, R Hsu, L S Keir, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 21, 2017
High Incomplete Skeletal Muscle Fatty Acid Oxidation Explains Low Muscle Insulin Sensitivity in Poorly Controlled T2D
Timothy P Gavin, Jacob M Ernst, Hyo-Bum Kwak, et al.
Page
of 102
Search research articles
Search
Showing results (751-760 of 1,012) with videos related to
Sort By:
Page
of 102
Neuroimage
|
November 9, 2022
CerebNet: A fast and reliable deep-learning pipeline for detailed cerebellum sub-segmentation
Jennifer Faber, David Kügler, Emad Bahrami, et al.
Nature Medicine
|
April 15, 2020
Adaptive evolution of virulence and persistence in carbapenem-resistant Klebsiella pneumoniae
Christoph M Ernst, Julian R Braxton, Carlos A Rodriguez-Osorio, et al.
Journal of Neurodevelopmental Disorders
|
December 16, 2022
Long-term follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder: corpus callosum white matter microstructure and neurocognitive outcomes
Blake A Gimbel, Mary E Anthony, Abigail M Ernst, et al.
Forensic Science International
|
March 12, 2004
Results of a collaborative study of the EDNAP group regarding mitochondrial DNA heteroplasmy and segregation in hair shafts
G Tully, S M Barritt, K Bender, et al.
The Journal of Pediatrics
|
August 28, 2023
Differences in Quality of Life in Children Across the Spectrum of Congenital Heart Disease
Amy M O'Connor, Amy Cassedy, Jo Wray, et al.
Annals of Clinical Biochemistry
|
July 11, 2006
Predictors of elevated cardiac troponin T on admission in ST-segment elevation myocardial infarction
Saman Rasoul, Mark B Nienhuis, Jan Paul Ottervanger, et al.
Journal of Pediatric Psychology
|
July 22, 2025
Stigma in differences of sex development: a scoping review
Canice E Crerand, Kristina I Suorsa-Johnson, Michelle M Ernst, et al.
Nature Reviews. Clinical Oncology
|
March 15, 2025
Utilizing ctDNA to discover mechanisms of resistance to targeted therapies in patients with metastatic NSCLC: towards more informative trials
Sophie M Ernst, Mihaela Aldea, Jan H von der Thüsen, et al.
American Journal of Human Genetics
|
October 10, 2007
Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
M A Simpson, R Hsu, L S Keir, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 21, 2017
High Incomplete Skeletal Muscle Fatty Acid Oxidation Explains Low Muscle Insulin Sensitivity in Poorly Controlled T2D
Timothy P Gavin, Jacob M Ernst, Hyo-Bum Kwak, et al.
Page
of 102