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Showing results (181-190 of 199) with videos related to

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Journal of Pediatric Surgery|July 5, 2020
Limiting hospital resources for acute appendicitis in children: Lessons learned from the U.S. epicenter of the COVID-19 pandemicCharlotte L Kvasnovsky, Yan Shi, Barrie S Rich, et al.
Journal of Cardiovascular Translational Research|November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic CardiomyopathyTomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Frontiers in Psychology|October 9, 2023
Psychometric properties of the 52-, 25-, and 10-item English and Spanish versions of the Social Problem-Solving Inventory-RevisedSasja A Schepers, Sean Phipps, Katie A Devine, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2023
Limb girdle muscular disease caused by <i>HMGCR</i> mutation and statin myopathy treatable with mevalonolactoneYuval Yogev, Zamir Shorer, Arie Koifman, et al.
Clinical Ophthalmology (Auckland, N.Z.)|July 8, 2021
The Impact of Inherited Retinal Diseases in the United States of America (US) and Canada from a Cost-of-Illness PerspectiveJennifer Gong, Simone Cheung, Alivia Fasso-Opie, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|April 3, 2013
Evaluation of the psychometric properties of the Pediatric Parenting Stress Inventory (PPSI)Katie A Devine, Charles E Heckler, Ernest R Katz, et al.
JIMD Reports|January 10, 2025
Severe neonatal hypotonia due to <i>SLC30A5</i> variant affecting function of ZnT5 zinc transporterVadim Dolgin, Pauline Chabosseau, Jacob Bistritzer, et al.
Nature Communications|October 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and miceD Halperin, A Stavsky, R Kadir, et al.
Journal of Medical Genetics|July 3, 2023
<i>SMARCA4</i> mutation causes human otosclerosis and a similar phenotype in miceMax Drabkin, Matan M Jean, Yael Noy, et al.
Eclinicalmedicine|July 9, 2020
In-person vs. web-based administration of a problem-solving skills intervention for parents of children with cancer: Report of a randomized noninferiority trialSean Phipps, Diane L Fairclough, Robert B Noll, et al.
Pageof 20

Showing results (181-190 of 199) with videos related to

Sort By:
Pageof 20
Journal of Pediatric Surgery|July 5, 2020
Limiting hospital resources for acute appendicitis in children: Lessons learned from the U.S. epicenter of the COVID-19 pandemicCharlotte L Kvasnovsky, Yan Shi, Barrie S Rich, et al.
Journal of Cardiovascular Translational Research|November 16, 2023
Compound Heterozygosity for Late-Onset Cardiomyopathy-Causative ALPK3 Coding Variant and Novel Intronic Variant Cause Infantile Hypertrophic CardiomyopathyTomer Poleg, Marina Eskin-Schwartz, Regina Proskorovski-Ohayon, et al.
Frontiers in Psychology|October 9, 2023
Psychometric properties of the 52-, 25-, and 10-item English and Spanish versions of the Social Problem-Solving Inventory-RevisedSasja A Schepers, Sean Phipps, Katie A Devine, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2023
Limb girdle muscular disease caused by <i>HMGCR</i> mutation and statin myopathy treatable with mevalonolactoneYuval Yogev, Zamir Shorer, Arie Koifman, et al.
Clinical Ophthalmology (Auckland, N.Z.)|July 8, 2021
The Impact of Inherited Retinal Diseases in the United States of America (US) and Canada from a Cost-of-Illness PerspectiveJennifer Gong, Simone Cheung, Alivia Fasso-Opie, et al.
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|April 3, 2013
Evaluation of the psychometric properties of the Pediatric Parenting Stress Inventory (PPSI)Katie A Devine, Charles E Heckler, Ernest R Katz, et al.
JIMD Reports|January 10, 2025
Severe neonatal hypotonia due to <i>SLC30A5</i> variant affecting function of ZnT5 zinc transporterVadim Dolgin, Pauline Chabosseau, Jacob Bistritzer, et al.
Nature Communications|October 27, 2021
CDH2 mutation affecting N-cadherin function causes attention-deficit hyperactivity disorder in humans and miceD Halperin, A Stavsky, R Kadir, et al.
Journal of Medical Genetics|July 3, 2023
<i>SMARCA4</i> mutation causes human otosclerosis and a similar phenotype in miceMax Drabkin, Matan M Jean, Yael Noy, et al.
Eclinicalmedicine|July 9, 2020
In-person vs. web-based administration of a problem-solving skills intervention for parents of children with cancer: Report of a randomized noninferiority trialSean Phipps, Diane L Fairclough, Robert B Noll, et al.
Pageof 20