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Ruth Armstrong

Showing results (31-40 of 61) with videos related to

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Movement Disorders Clinical Practice|July 31, 2024
Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual PathologyAinara Salazar-Villacorta, Robert Spaull, Samyami Chowdhury, et al.
British Journal of Cancer|April 22, 2022
The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancerJamie Trotman, Ruth Armstrong, Helen Firth, et al.
BMC Medical Education|November 7, 2024
Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practiceMichelle Bishop, Aditi Vedi, Sarah Bowdin, et al.
Pediatric Blood & Cancer|October 9, 2024
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumorShathar Mahmood, Sarah M Leiter, Poe Phyu, et al.
British Journal of Cancer|July 12, 2024
Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcomaJames A Watkins, Jamie Trotman, John A Tadross, et al.
Frontiers in Endocrinology|November 28, 2022
The use of temozolomide in paediatric metastatic phaeochromocytoma/paraganglioma: A case report and literature reviewCalum Urquhart, Ben Fleming, Ines Harper, et al.
American Journal of Medical Genetics. Part A|January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Clinical Endocrinology|May 21, 2020
Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohortSashi Mariathasan, Katrina A Andrews, Edward Thompson, et al.
International Journal of Cancer|January 12, 2026
Outcomes from the English National Lynch Syndrome transformation projectKevin J Monahan, Paul Fleming, Neil A J Ryan, et al.
BMJ Oncology|January 31, 2025
The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programmeKevin J Monahan, Neil Ryan, Laura Monje-Garcia, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Movement Disorders Clinical Practice|July 31, 2024
Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual PathologyAinara Salazar-Villacorta, Robert Spaull, Samyami Chowdhury, et al.
British Journal of Cancer|April 22, 2022
The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancerJamie Trotman, Ruth Armstrong, Helen Firth, et al.
BMC Medical Education|November 7, 2024
Identifying barriers and opportunities to facilitate the uptake of whole genome sequencing in paediatric haematology and oncology practiceMichelle Bishop, Aditi Vedi, Sarah Bowdin, et al.
Pediatric Blood & Cancer|October 9, 2024
A diagnosis of Noonan syndrome through routine whole genome sequencing in a child with an intracranial nongerminomatous germ cell tumorShathar Mahmood, Sarah M Leiter, Poe Phyu, et al.
British Journal of Cancer|July 12, 2024
Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcomaJames A Watkins, Jamie Trotman, John A Tadross, et al.
Frontiers in Endocrinology|November 28, 2022
The use of temozolomide in paediatric metastatic phaeochromocytoma/paraganglioma: A case report and literature reviewCalum Urquhart, Ben Fleming, Ines Harper, et al.
American Journal of Medical Genetics. Part A|January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
Clinical Endocrinology|May 21, 2020
Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohortSashi Mariathasan, Katrina A Andrews, Edward Thompson, et al.
International Journal of Cancer|January 12, 2026
Outcomes from the English National Lynch Syndrome transformation projectKevin J Monahan, Paul Fleming, Neil A J Ryan, et al.
BMJ Oncology|January 31, 2025
The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programmeKevin J Monahan, Neil Ryan, Laura Monje-Garcia, et al.
Pageof 7