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Menachem Gross

Showing results (81-90 of 99) with videos related to

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Audiology & Neuro-Otology|June 17, 2006
Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing lossMenachem Gross, Gideon Friedman, Ron Eliashar, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|September 9, 2019
The association between video-nystagmography and sensory organization test of computerized dynamic posturography in patients with vestibular symptomsShany G Gofrit, Ophir Ilan, Yulia Mayler, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Audiology Research|January 21, 2026
Video Head Impulse Test: A Prognostic Marker for Patients with Idiopathic Sudden Sensorineural Hearing LossGaelle Ngankam Fotsing Epse Vofo, Matityahou Ormianer, Marrigje Aagje de Jong, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
International Microbiology : the Official Journal of the Spanish Society for Microbiology|September 10, 2021
Sustained release varnish containing chlorhexidine for prevention of Streptococcus mutans biofilm formation on voice prosthesis surface: an in vitro studyMenachem Gross, Fadi Ashqar, Ronit Vogt Sionov, et al.
Pharmaceutics|April 26, 2025
The Incorporation of CBD into Biodegradable DL-Lactide/Glycolide Copolymers Creates a Persistent Antibacterial Environment: An In Vitro Study on <i>Streptococcus mutans</i> and <i>Staphylococcus aureus</i>Ronit Vogt Sionov, Ahmad Siag, Emma Theresa Mersini, et al.
Translational Vision Science & Technology|March 1, 2023
Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in MiceAlaa Abu-Diab, Prakadeeswari Gopalakrishnan, Chen Matsevich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humansSamer Khateb, Björn Kowalewski, Nicola Bedoni, et al.
Plos Biology|June 12, 2025
Mutant EZH2 alters the epigenetic network and increases epigenetic heterogeneity in B cell lymphomaOfir Griess, Noa Furth, Nofar Harpaz, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Audiology & Neuro-Otology|June 17, 2006
Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing lossMenachem Gross, Gideon Friedman, Ron Eliashar, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|September 9, 2019
The association between video-nystagmography and sensory organization test of computerized dynamic posturography in patients with vestibular symptomsShany G Gofrit, Ophir Ilan, Yulia Mayler, et al.
Plos One|December 20, 2012
Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing lossSamer Khateb, Lina Zelinger, Tamar Ben-Yosef, et al.
Audiology Research|January 21, 2026
Video Head Impulse Test: A Prognostic Marker for Patients with Idiopathic Sudden Sensorineural Hearing LossGaelle Ngankam Fotsing Epse Vofo, Matityahou Ormianer, Marrigje Aagje de Jong, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
International Microbiology : the Official Journal of the Spanish Society for Microbiology|September 10, 2021
Sustained release varnish containing chlorhexidine for prevention of Streptococcus mutans biofilm formation on voice prosthesis surface: an in vitro studyMenachem Gross, Fadi Ashqar, Ronit Vogt Sionov, et al.
Pharmaceutics|April 26, 2025
The Incorporation of CBD into Biodegradable DL-Lactide/Glycolide Copolymers Creates a Persistent Antibacterial Environment: An In Vitro Study on <i>Streptococcus mutans</i> and <i>Staphylococcus aureus</i>Ronit Vogt Sionov, Ahmad Siag, Emma Theresa Mersini, et al.
Translational Vision Science & Technology|March 1, 2023
Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in MiceAlaa Abu-Diab, Prakadeeswari Gopalakrishnan, Chen Matsevich, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humansSamer Khateb, Björn Kowalewski, Nicola Bedoni, et al.
Plos Biology|June 12, 2025
Mutant EZH2 alters the epigenetic network and increases epigenetic heterogeneity in B cell lymphomaOfir Griess, Noa Furth, Nofar Harpaz, et al.
Pageof 10