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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 29, 2019
Chronic kidney disease in propionic acidemia
Oleg A Shchelochkov, Irini Manoli, Jennifer L Sloan, et al.
The British Journal of Ophthalmology
|
June 27, 2022
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome
Laryssa A Huryn, Taylor Flaherty, Rosalie Nolen, et al.
Diagnostics (Basel, Switzerland)
|
June 24, 2022
Airflow Obstruction in Adults with Williams Syndrome and Mice with Elastin Insufficiency
Elise K Kronquist, Maninder Kaur, Leah M Gober, et al.
Human Molecular Genetics
|
February 17, 2018
Conditional ablation and conditional rescue models for Casq2 elucidate the role of development and of cell-type specific expression of Casq2 in the CPVT2 phenotype
Daniel J Flores, ThuyVy Duong, Luke O Brandenberger, et al.
The Journal of Pediatrics
|
August 31, 2016
Hypercalcemia in Patients with Williams-Beuren Syndrome
Sampat Sindhar, Michael Lugo, Mark D Levin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 21, 2009
Cardiomyocyte cyclooxygenase-2 influences cardiac rhythm and function
Dairong Wang, Vickas V Patel, Emanuela Ricciotti, et al.
Frontiers in Cardiovascular Medicine
|
June 6, 2022
Elastin Insufficiency Confers Proximal and Distal Pulmonary Vasculopathy in Mice, Partially Remedied by the K<sub>ATP</sub> Channel Opener Minoxidil: Considerations and Cautions for the Treatment of People With Williams-Beuren Syndrome
Russell H Knutsen, Leah M Gober, Elise K Kronquist, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 29, 2021
X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model
Mark D Levin, Simona Bianconi, Andrew Smith, et al.
The Journal of Clinical Investigation
|
October 27, 2009
Melanocyte-like cells in the heart and pulmonary veins contribute to atrial arrhythmia triggers
Mark D Levin, Min Min Lu, Nataliya B Petrenko, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 29, 2019
Chronic kidney disease in propionic acidemia
Oleg A Shchelochkov, Irini Manoli, Jennifer L Sloan, et al.
The British Journal of Ophthalmology
|
June 27, 2022
Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome
Laryssa A Huryn, Taylor Flaherty, Rosalie Nolen, et al.
Diagnostics (Basel, Switzerland)
|
June 24, 2022
Airflow Obstruction in Adults with Williams Syndrome and Mice with Elastin Insufficiency
Elise K Kronquist, Maninder Kaur, Leah M Gober, et al.
Human Molecular Genetics
|
February 17, 2018
Conditional ablation and conditional rescue models for Casq2 elucidate the role of development and of cell-type specific expression of Casq2 in the CPVT2 phenotype
Daniel J Flores, ThuyVy Duong, Luke O Brandenberger, et al.
The Journal of Pediatrics
|
August 31, 2016
Hypercalcemia in Patients with Williams-Beuren Syndrome
Sampat Sindhar, Michael Lugo, Mark D Levin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 21, 2009
Cardiomyocyte cyclooxygenase-2 influences cardiac rhythm and function
Dairong Wang, Vickas V Patel, Emanuela Ricciotti, et al.
Frontiers in Cardiovascular Medicine
|
June 6, 2022
Elastin Insufficiency Confers Proximal and Distal Pulmonary Vasculopathy in Mice, Partially Remedied by the K<sub>ATP</sub> Channel Opener Minoxidil: Considerations and Cautions for the Treatment of People With Williams-Beuren Syndrome
Russell H Knutsen, Leah M Gober, Elise K Kronquist, et al.
American Journal of Medical Genetics. Part A
|
July 29, 2018
Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients
Mark D Levin, Sulagna C Saitta, Karen W Gripp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 29, 2021
X-linked creatine transporter deficiency results in prolonged QTc and increased sudden death risk in humans and disease model
Mark D Levin, Simona Bianconi, Andrew Smith, et al.
The Journal of Clinical Investigation
|
October 27, 2009
Melanocyte-like cells in the heart and pulmonary veins contribute to atrial arrhythmia triggers
Mark D Levin, Min Min Lu, Nataliya B Petrenko, et al.
Page
of 7