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Showing results (941-950 of 968) with videos related to

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Annals of Internal Medicine|November 16, 2021
Comparative Effectiveness of an Automated Text Messaging Service for Monitoring COVID-19 at HomeM Kit Delgado, Anna U Morgan, David A Asch, et al.
American Journal of Surgery|September 19, 2017
A multi-institutional analysis of intraoperative radiotherapy for early breast cancer: Does age matter?A M Abbott, S A Valente, L Loftus, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.
Internal Medicine Journal|September 5, 2024
6-Thioguanine nucleotide levels are associated with infliximab but not adalimumab levels in inflammatory bowel disease patients on combination therapyNatalie Yu, Tanya Lee, Daniel Tassone, et al.
Journal of Alzheimer'S Disease Reports|October 22, 2025
Harnessing team science in dementia research: Insights from the Alzheimer's disease research group in South CarolinaSayema Akter, Eric Mishio Bawa, Nicholas Riccardi, et al.
Nature Genetics|October 28, 2008
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humansZubair M Ahmed, Saber Masmoudi, Ersan Kalay, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
American Journal of Human Genetics|January 26, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, et al.
Human Mutation|October 11, 2018
Global genetic insight contributed by consanguineous Pakistani families segregating hearing lossElodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 97

Showing results (941-950 of 968) with videos related to

Sort By:
Pageof 97
Annals of Internal Medicine|November 16, 2021
Comparative Effectiveness of an Automated Text Messaging Service for Monitoring COVID-19 at HomeM Kit Delgado, Anna U Morgan, David A Asch, et al.
American Journal of Surgery|September 19, 2017
A multi-institutional analysis of intraoperative radiotherapy for early breast cancer: Does age matter?A M Abbott, S A Valente, L Loftus, et al.
American Journal of Human Genetics|January 7, 2014
Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86Atteeq U Rehman, Regie Lyn P Santos-Cortez, Robert J Morell, et al.
Internal Medicine Journal|September 5, 2024
6-Thioguanine nucleotide levels are associated with infliximab but not adalimumab levels in inflammatory bowel disease patients on combination therapyNatalie Yu, Tanya Lee, Daniel Tassone, et al.
Journal of Alzheimer'S Disease Reports|October 22, 2025
Harnessing team science in dementia research: Insights from the Alzheimer's disease research group in South CarolinaSayema Akter, Eric Mishio Bawa, Nicholas Riccardi, et al.
Nature Genetics|October 28, 2008
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humansZubair M Ahmed, Saber Masmoudi, Ersan Kalay, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
American Journal of Human Genetics|January 26, 2016
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2Regie Lyn P Santos-Cortez, Rabia Faridi, Atteeq U Rehman, et al.
Human Mutation|October 11, 2018
Global genetic insight contributed by consanguineous Pakistani families segregating hearing lossElodie M Richard, Regie Lyn P Santos-Cortez, Rabia Faridi, et al.
American Journal of Human Genetics|June 21, 2002
CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafnessL M Astuto, J M Bork, M D Weston, et al.
Pageof 97