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Sarah Montgomery

Showing results (21-30 of 29) with videos related to

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Journal of the National Comprehensive Cancer Network : JNCCN|April 9, 2025
NCCN Guidelines® Insights: Testicular Cancer, Version 2.2025Timothy Gilligan, Daniel W Lin, Nabil Adra, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|September 5, 2024
Cancer-Associated Venous Thromboembolic Disease, Version 2.2024, NCCN Clinical Practice Guidelines in OncologyMichael B Streiff, Bjorn Holmstrom, Dana Angelini, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|August 7, 2023
Adolescent and Young Adult (AYA) Oncology, Version 2.2024, NCCN Clinical Practice Guidelines in OncologySmita Bhatia, Alberto S Pappo, Melissa Acquazzino, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|April 9, 2026
NCCN Guidelines® Insights: Distress Management, Version 1.2026Jesse R Fann, Jessica Vanderlan, Benjamin W Brewer, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|February 11, 2026
Hodgkin Lymphoma, Version 1.2026, NCCN Clinical Practice Guidelines In OncologyRanjana H Advani, Christopher R Kelsey, Philippe Armand, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|February 12, 2025
NCCN Guidelines® Insights: Head and Neck Cancers, Version 2.2025A Dimitrios Colevas, Anthony J Cmelak, David G Pfister, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalitiesFuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
American Journal of Human Genetics|December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotypeSusan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
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Showing results (21-30 of 29) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of the National Comprehensive Cancer Network : JNCCN|April 9, 2025
NCCN Guidelines® Insights: Testicular Cancer, Version 2.2025Timothy Gilligan, Daniel W Lin, Nabil Adra, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|September 5, 2024
Cancer-Associated Venous Thromboembolic Disease, Version 2.2024, NCCN Clinical Practice Guidelines in OncologyMichael B Streiff, Bjorn Holmstrom, Dana Angelini, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|August 7, 2023
Adolescent and Young Adult (AYA) Oncology, Version 2.2024, NCCN Clinical Practice Guidelines in OncologySmita Bhatia, Alberto S Pappo, Melissa Acquazzino, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|April 9, 2026
NCCN Guidelines® Insights: Distress Management, Version 1.2026Jesse R Fann, Jessica Vanderlan, Benjamin W Brewer, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|February 11, 2026
Hodgkin Lymphoma, Version 1.2026, NCCN Clinical Practice Guidelines In OncologyRanjana H Advani, Christopher R Kelsey, Philippe Armand, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|February 12, 2025
NCCN Guidelines® Insights: Head and Neck Cancers, Version 2.2025A Dimitrios Colevas, Anthony J Cmelak, David G Pfister, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalitiesFuad Chowdhury, Lei Wang, Mohammed Al-Raqad, et al.
American Journal of Human Genetics|December 31, 2022
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotypeSusan M Hiatt, Slavica Trajkova, Matteo Rossi Sebastiano, et al.
Pageof 3