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IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society
|
April 12, 2014
Learning joint intensity-depth sparse representations
Ivana Tosic, Sarah Drewes
SAGE Open Medical Case Reports
|
April 2, 2021
A familial case of <i>CAMK2B</i> mutation with variable expressivity
Paige Heiman, Sarah Drewes, Lina Ghaloul-Gonzalez
Journal of Pharmaceutical Sciences
|
July 8, 2023
Image Classification of Degraded Polysorbate, Protein and Silicone Oil Sub-Visible Particles Detected by Flow-Imaging Microscopy in Biopharmaceuticals Using a Convolutional Neural Network Model
Filip M Fedorowicz, Pascal Chalus, Kyra Kirschenbühler, et al.
Preventing Chronic Disease
|
May 6, 2018
We Run This City: Impact of a Community-School Fitness Program on Obesity, Health, and Fitness
Elaine A Borawski, Sarah Drewes Jones, Laura Danosky Yoder, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2021
Reproductive outcomes in individuals with chromosomal reciprocal translocations
Angela Verdoni, Jie Hu, Urvashi Surti, et al.
International Journal of Neonatal Screening
|
April 25, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in Pennsylvania
Jessica R C Priestley, Laura A Adang, Sarah Drewes Williams, et al.
Brain : a Journal of Neurology
|
December 27, 2021
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis
Macarena Cabrera-Serrano, Laure Caccavelli, Marco Savarese, et al.
American Journal of Human Genetics
|
March 13, 2024
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
Xueyang Pan, Alice M Tao, Shenzhao Lu, et al.
Brain : a Journal of Neurology
|
August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis
Arthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification
Tobias Brünger, Ilona Krey, Suyeon Kim, et al.
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
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IEEE Transactions on Image Processing : a Publication of the IEEE Signal Processing Society
|
April 12, 2014
Learning joint intensity-depth sparse representations
Ivana Tosic, Sarah Drewes
SAGE Open Medical Case Reports
|
April 2, 2021
A familial case of <i>CAMK2B</i> mutation with variable expressivity
Paige Heiman, Sarah Drewes, Lina Ghaloul-Gonzalez
Journal of Pharmaceutical Sciences
|
July 8, 2023
Image Classification of Degraded Polysorbate, Protein and Silicone Oil Sub-Visible Particles Detected by Flow-Imaging Microscopy in Biopharmaceuticals Using a Convolutional Neural Network Model
Filip M Fedorowicz, Pascal Chalus, Kyra Kirschenbühler, et al.
Preventing Chronic Disease
|
May 6, 2018
We Run This City: Impact of a Community-School Fitness Program on Obesity, Health, and Fitness
Elaine A Borawski, Sarah Drewes Jones, Laura Danosky Yoder, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2021
Reproductive outcomes in individuals with chromosomal reciprocal translocations
Angela Verdoni, Jie Hu, Urvashi Surti, et al.
International Journal of Neonatal Screening
|
April 25, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in Pennsylvania
Jessica R C Priestley, Laura A Adang, Sarah Drewes Williams, et al.
Brain : a Journal of Neurology
|
December 27, 2021
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis
Macarena Cabrera-Serrano, Laure Caccavelli, Marco Savarese, et al.
American Journal of Human Genetics
|
March 13, 2024
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features
Xueyang Pan, Alice M Tao, Shenzhao Lu, et al.
Brain : a Journal of Neurology
|
August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis
Arthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification
Tobias Brünger, Ilona Krey, Suyeon Kim, et al.
Page
of 1