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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 pandemic
Charlotte 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 Cardiomyopathy
Tomer 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-Revised
Sasja 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 mevalonolactone
Yuval 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 Perspective
Jennifer 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 transporter
Vadim 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 mice
D 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 mice
Max 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 trial
Sean Phipps, Diane L Fairclough, Robert B Noll, et al.
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of 20
Search research articles
Search
Showing results (181-190 of 199) with videos related to
Sort By:
Page
of 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 pandemic
Charlotte 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 Cardiomyopathy
Tomer 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-Revised
Sasja 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 mevalonolactone
Yuval 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 Perspective
Jennifer 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 transporter
Vadim 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 mice
D 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 mice
Max 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 trial
Sean Phipps, Diane L Fairclough, Robert B Noll, et al.
Page
of 20