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The Journal of Pediatrics
|
June 2, 2006
Acute liver failure in children: the first 348 patients in the pediatric acute liver failure study group
Robert H Squires, Benjamin L Shneider, John Bucuvalas, et al.
American Journal of Human Genetics
|
May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
Jeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine
|
March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
Frederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Pediatrics
|
January 6, 2010
Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report
Timothy Buie, Daniel B Campbell, George J Fuchs, et al.
Human Mutation
|
July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays
Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Clinical Diabetes : a Publication of the American Diabetes Association
|
January 20, 2025
Culturally Congruent Latino-Adapted Telemonitoring of Underrepresented Adults With Type 2 Diabetes: The CULTURA-DM2 Trial
Renee Pekmezaris, Sabrina Martinez, Valeria Correa Gomez, et al.
The Annals of Thoracic Surgery
|
July 2, 2011
Successful linking of the Society of Thoracic Surgeons database to social security data to examine survival after cardiac operations
Jeffrey Phillip Jacobs, Fred H Edwards, David M Shahian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing
Christopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Science (New York, N.Y.)
|
December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 15, 2019
Clinical Practice Approach to Nonalcoholic Fatty Liver Disease by Pediatric Gastroenterologists in the United States
Warren L Shapiro, Elizabeth L Yu, Jennifer C Arin, et al.
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of 100
Search research articles
Search
Showing results (971-980 of 996) with videos related to
Sort By:
Page
of 100
The Journal of Pediatrics
|
June 2, 2006
Acute liver failure in children: the first 348 patients in the pediatric acute liver failure study group
Robert H Squires, Benjamin L Shneider, John Bucuvalas, et al.
American Journal of Human Genetics
|
May 5, 2018
Profiling and Leveraging Relatedness in a Precision Medicine Cohort of 92,455 Exomes
Jeffrey Staples, Evan K Maxwell, Nehal Gosalia, et al.
The New England Journal of Medicine
|
March 3, 2016
Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease
Frederick E Dewey, Viktoria Gusarova, Colm O'Dushlaine, et al.
Pediatrics
|
January 6, 2010
Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report
Timothy Buie, Daniel B Campbell, George J Fuchs, et al.
Human Mutation
|
July 24, 2013
Recurrent HERV-H-mediated 3q13.2-q13.31 deletions cause a syndrome of hypotonia and motor, language, and cognitive delays
Andrey Shuvarikov, Ian M Campbell, Piotr Dittwald, et al.
Clinical Diabetes : a Publication of the American Diabetes Association
|
January 20, 2025
Culturally Congruent Latino-Adapted Telemonitoring of Underrepresented Adults With Type 2 Diabetes: The CULTURA-DM2 Trial
Renee Pekmezaris, Sabrina Martinez, Valeria Correa Gomez, et al.
The Annals of Thoracic Surgery
|
July 2, 2011
Successful linking of the Society of Thoracic Surgeons database to social security data to examine survival after cardiac operations
Jeffrey Phillip Jacobs, Fred H Edwards, David M Shahian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing
Christopher M Haggerty, Cynthia A James, Hugh Calkins, et al.
Science (New York, N.Y.)
|
December 24, 2016
Genetic identification of familial hypercholesterolemia within a single U.S. health care system
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
January 15, 2019
Clinical Practice Approach to Nonalcoholic Fatty Liver Disease by Pediatric Gastroenterologists in the United States
Warren L Shapiro, Elizabeth L Yu, Jennifer C Arin, et al.
Page
of 100