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James T Bennett

Showing results (51-60 of 83) with videos related to

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International Journal of Pediatric Otorhinolaryngology|September 19, 2021
Acetylsalicylic acid suppression of the PI3K pathway as a novel medical therapy for head and neck lymphatic malformationsJuliana Bonilla-Velez, Kathryn B Whitlock, Sheila Ganti, et al.
International Journal of Pediatric Otorhinolaryngology|December 2, 2022
Primary targeted medical therapy for management of bilateral head and neck lymphatic malformations in infantsClare M Richardson, Jonathan N Perkins, Kaitlyn Zenner, et al.
HGG Advances|April 4, 2022
Somatic activating <i>BRAF</i> variants cause isolated lymphatic malformationsKaitlyn Zenner, Dana M Jensen, Victoria Dmyterko, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|December 13, 2016
Factors affecting the outcome in appearance of AIS surgery in terms of the minimal clinically important differenceJames T Bennett, Amer F Samdani, Tracey P Bastrom, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
Immune dysfunction in MGAT2-CDG: A clinical report and review of the literatureSheri A Poskanzer, Matthew J Schultz, Coleman T Turgeon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowthTara L Wenger, Sheila Ganti, Catherine Bull, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2026
Mutations in VCP cause Adams-Oliver syndrome with or without pulmonary hypertensionAnna Lehman, Sana Ahmed, Arezoo Mohajeri, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.
American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.
Journal of Medical Genetics|January 4, 2014
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic herniaLan Yu, James T Bennett, Julia Wynn, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
International Journal of Pediatric Otorhinolaryngology|September 19, 2021
Acetylsalicylic acid suppression of the PI3K pathway as a novel medical therapy for head and neck lymphatic malformationsJuliana Bonilla-Velez, Kathryn B Whitlock, Sheila Ganti, et al.
International Journal of Pediatric Otorhinolaryngology|December 2, 2022
Primary targeted medical therapy for management of bilateral head and neck lymphatic malformations in infantsClare M Richardson, Jonathan N Perkins, Kaitlyn Zenner, et al.
HGG Advances|April 4, 2022
Somatic activating <i>BRAF</i> variants cause isolated lymphatic malformationsKaitlyn Zenner, Dana M Jensen, Victoria Dmyterko, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|December 13, 2016
Factors affecting the outcome in appearance of AIS surgery in terms of the minimal clinically important differenceJames T Bennett, Amer F Samdani, Tracey P Bastrom, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
Immune dysfunction in MGAT2-CDG: A clinical report and review of the literatureSheri A Poskanzer, Matthew J Schultz, Coleman T Turgeon, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowthTara L Wenger, Sheila Ganti, Catherine Bull, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2026
Mutations in VCP cause Adams-Oliver syndrome with or without pulmonary hypertensionAnna Lehman, Sana Ahmed, Arezoo Mohajeri, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.
American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.
Journal of Medical Genetics|January 4, 2014
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic herniaLan Yu, James T Bennett, Julia Wynn, et al.
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