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Showing results (41-50 of 96) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|November 13, 2018
Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 DeficiencyAlina Kurolap, Orly Eshach Adiv, Tova Hershkovitz, et al.
NAR Genomics and Bioinformatics|January 9, 2025
Long-read structural and epigenetic profiling of a kidney tumor-matched sample with nanopore sequencing and optical genome mappingSapir Margalit, Zuzana Tulpová, Tahir Detinis Zur, et al.
Biorxiv : the Preprint Server for Biology|June 25, 2024
Long-Read Structural and Epigenetic Profiling of a Kidney Tumor-Matched Sample with Nanopore Sequencing and Optical Genome MappingSapir Margalit, Zuzana Tulpová, Tahir Detinis Zur, et al.
Journal of Molecular Neuroscience : MN|June 8, 2022
Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison ExonPenina Ponger, Alina Kurolap, Israela Lerer, et al.
Genetics in Medicine Open|December 13, 2024
Publicly funded exome sequencing for outpatients with neurodevelopmental disorders demonstrates a high rate of unexpected findings impacting medical managementYara Nakhleh Francis, Tova Hershkovitz, Nina Ekhilevitch, et al.
Scientific Reports|September 13, 2024
The d3GHR carrier epigenome in Druze clan longevityGhadeer Falah, Alina Kurolap, Tamar Paperna, et al.
Clinical Dysmorphology|September 14, 2020
A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1Amir Peleg, Alina Kurolap, Lena Sagi-Dain, et al.
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Prenatal Diagnosis|December 2, 2025
Diagnostic Value of Exome Sequencing in Isolated PolyhydramniosVered Offen Glassner, Adi Botvinik, Adi Mory, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|November 9, 2023
Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction RatesUri Hamiel, Audelia Eshel Fuhrer, Nitsan Landau, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Journal of Pediatric Gastroenterology and Nutrition|November 13, 2018
Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 DeficiencyAlina Kurolap, Orly Eshach Adiv, Tova Hershkovitz, et al.
NAR Genomics and Bioinformatics|January 9, 2025
Long-read structural and epigenetic profiling of a kidney tumor-matched sample with nanopore sequencing and optical genome mappingSapir Margalit, Zuzana Tulpová, Tahir Detinis Zur, et al.
Biorxiv : the Preprint Server for Biology|June 25, 2024
Long-Read Structural and Epigenetic Profiling of a Kidney Tumor-Matched Sample with Nanopore Sequencing and Optical Genome MappingSapir Margalit, Zuzana Tulpová, Tahir Detinis Zur, et al.
Journal of Molecular Neuroscience : MN|June 8, 2022
Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison ExonPenina Ponger, Alina Kurolap, Israela Lerer, et al.
Genetics in Medicine Open|December 13, 2024
Publicly funded exome sequencing for outpatients with neurodevelopmental disorders demonstrates a high rate of unexpected findings impacting medical managementYara Nakhleh Francis, Tova Hershkovitz, Nina Ekhilevitch, et al.
Scientific Reports|September 13, 2024
The d3GHR carrier epigenome in Druze clan longevityGhadeer Falah, Alina Kurolap, Tamar Paperna, et al.
Clinical Dysmorphology|September 14, 2020
A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1Amir Peleg, Alina Kurolap, Lena Sagi-Dain, et al.
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Prenatal Diagnosis|December 2, 2025
Diagnostic Value of Exome Sequencing in Isolated PolyhydramniosVered Offen Glassner, Adi Botvinik, Adi Mory, et al.
Telemedicine Journal and E-Health : the Official Journal of the American Telemedicine Association|November 9, 2023
Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction RatesUri Hamiel, Audelia Eshel Fuhrer, Nitsan Landau, et al.
Pageof 10