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American Journal of Medical Genetics. Part A
|
October 1, 2024
Examining Roles, Challenges, and Opportunities Within the Metabolic Genetics Workforce
Kara Simpson, Stephanie Offord, Chanel Suares, et al.
JAAD Case Reports
|
March 5, 2021
Unexplained oral and extremity ulcerations in an infant
Kristen Russomanno, Ashley DiLorenzo, Kara Simpson, et al.
Journal of General Internal Medicine
|
June 24, 2026
Identifying Patterns of Stigmatizing Language Use in the Safety Net
Kriti Gogia, Zeyu Li, Kara Simpson, et al.
Neuromuscular Disorders : NMD
|
January 23, 2014
Novel large deletion in the ACTA1 gene in a child with autosomal recessive nemaline myopathy
Bethany Friedman, Kara Simpson, Carolina Tesi-Rocha, et al.
Journal of Medical Case Reports
|
May 13, 2025
High-dose flecainide for symptomatic relief in paramyotonia congenita/severe neonatal episodic laryngospasm due to SCN4A G1306E: a case report
Vanessa Ogueri, Jessica Chong, Melissa Fleming, et al.
Molecular Genetics and Metabolism
|
March 13, 2025
Maternal health outcomes in ornithine transcarbamylase deficiency: A comparative analysis of pregnancies in symptomatic and asymptomatic heterozygotes
Margo Sheck Breilyn, Kara Simpson, Sara A Elsbecker, et al.
Plos Pathogens
|
June 9, 2025
SOX9 plays an essential role in myofibroblast driven hepatic granuloma integrity and parenchymal repair during schistosomiasis-induced liver damage
Kim Su, Elliot Jokl, Alice Costain, et al.
JIMD Reports
|
May 12, 2025
Orthotopic Liver Transplantation in a Patient With <i>GALT</i>p.Ser135Leu/Null
Kara Simpson, Erin L MacLeod, Julia Clayton, et al.
Molecular Genetics and Metabolism
|
September 10, 2023
Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders
Chaya N Murali, John R Barber, Robert McCarter, et al.
Cells
|
June 28, 2023
Circadian Disruption Primes Myofibroblasts for Accelerated Activation as a Mechanism Underpinning Fibrotic Progression in Non-Alcoholic Fatty Liver Disease
Elliot Jokl, Jessica Llewellyn, Kara Simpson, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics. Part A
|
October 1, 2024
Examining Roles, Challenges, and Opportunities Within the Metabolic Genetics Workforce
Kara Simpson, Stephanie Offord, Chanel Suares, et al.
JAAD Case Reports
|
March 5, 2021
Unexplained oral and extremity ulcerations in an infant
Kristen Russomanno, Ashley DiLorenzo, Kara Simpson, et al.
Journal of General Internal Medicine
|
June 24, 2026
Identifying Patterns of Stigmatizing Language Use in the Safety Net
Kriti Gogia, Zeyu Li, Kara Simpson, et al.
Neuromuscular Disorders : NMD
|
January 23, 2014
Novel large deletion in the ACTA1 gene in a child with autosomal recessive nemaline myopathy
Bethany Friedman, Kara Simpson, Carolina Tesi-Rocha, et al.
Journal of Medical Case Reports
|
May 13, 2025
High-dose flecainide for symptomatic relief in paramyotonia congenita/severe neonatal episodic laryngospasm due to SCN4A G1306E: a case report
Vanessa Ogueri, Jessica Chong, Melissa Fleming, et al.
Molecular Genetics and Metabolism
|
March 13, 2025
Maternal health outcomes in ornithine transcarbamylase deficiency: A comparative analysis of pregnancies in symptomatic and asymptomatic heterozygotes
Margo Sheck Breilyn, Kara Simpson, Sara A Elsbecker, et al.
Plos Pathogens
|
June 9, 2025
SOX9 plays an essential role in myofibroblast driven hepatic granuloma integrity and parenchymal repair during schistosomiasis-induced liver damage
Kim Su, Elliot Jokl, Alice Costain, et al.
JIMD Reports
|
May 12, 2025
Orthotopic Liver Transplantation in a Patient With <i>GALT</i>p.Ser135Leu/Null
Kara Simpson, Erin L MacLeod, Julia Clayton, et al.
Molecular Genetics and Metabolism
|
September 10, 2023
Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders
Chaya N Murali, John R Barber, Robert McCarter, et al.
Cells
|
June 28, 2023
Circadian Disruption Primes Myofibroblasts for Accelerated Activation as a Mechanism Underpinning Fibrotic Progression in Non-Alcoholic Fatty Liver Disease
Elliot Jokl, Jessica Llewellyn, Kara Simpson, et al.
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of 2