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Paige Heiman

Showing results (1-10 of 6) with videos related to

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SAGE Open Medical Case Reports|April 2, 2021
A familial case of <i>CAMK2B</i> mutation with variable expressivityPaige Heiman, Sarah Drewes, Lina Ghaloul-Gonzalez
Children (Basel, Switzerland)|June 27, 2024
Analysis of Maternal and Congenital Syphilis Rates at a New Jersey University HospitalPaige Heiman, Vineet Bhandari, Sarah Davenport, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Natural history of propionic acidemia in the Amish populationSarah Ehrenberg, Catherine Walsh Vockley, Paige Heiman, et al.
Scientific Reports|February 24, 2022
Mitochondrial dysfunction associated with TANGO2 deficiencyPaige Heiman, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
American Journal of Medical Genetics. Part A|May 5, 2021
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approachRachel M Wolfe, Al-Walid Mohsen, Cate Walsh Vockley, et al.
Molecular Genetics and Metabolism Reports|November 7, 2022
ITCH deficiency clinical phenotype expansion and mitochondrial dysfunctionRachel Wolfe, Paige Heiman, Olivia D'Annibale, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
SAGE Open Medical Case Reports|April 2, 2021
A familial case of <i>CAMK2B</i> mutation with variable expressivityPaige Heiman, Sarah Drewes, Lina Ghaloul-Gonzalez
Children (Basel, Switzerland)|June 27, 2024
Analysis of Maternal and Congenital Syphilis Rates at a New Jersey University HospitalPaige Heiman, Vineet Bhandari, Sarah Davenport, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Natural history of propionic acidemia in the Amish populationSarah Ehrenberg, Catherine Walsh Vockley, Paige Heiman, et al.
Scientific Reports|February 24, 2022
Mitochondrial dysfunction associated with TANGO2 deficiencyPaige Heiman, Al-Walid Mohsen, Anuradha Karunanidhi, et al.
American Journal of Medical Genetics. Part A|May 5, 2021
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approachRachel M Wolfe, Al-Walid Mohsen, Cate Walsh Vockley, et al.
Molecular Genetics and Metabolism Reports|November 7, 2022
ITCH deficiency clinical phenotype expansion and mitochondrial dysfunctionRachel Wolfe, Paige Heiman, Olivia D'Annibale, et al.
Pageof 1