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Tamar Paperna

Showing results (11-20 of 50) with videos related to

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European Journal of Medical Genetics|January 9, 2025
A family with an atypical presentation of TBX3-related disorderKhaled Osman, Ayman Asaly, Rana Halloun, et al.
Rambam Maimonides Medical Journal|August 9, 2018
Rare Disease Diagnostics: A Single-center Experience and Lessons LearntKarin Weiss, Alina Kurolap, Tamar Paperna, et al.
Journal of the Neurological Sciences|September 16, 2008
Translation towards personalized medicine in Multiple SclerosisAriel Miller, Nili Avidan, Noa Tzunz-Henig, et al.
European Journal of Medical Genetics|February 7, 2024
Rapid exome sequencing for children with severe acute encephalopathy - A case seriesClair Habib, Tamar Paperna, Rinat Zaid, et al.
Pediatric Blood & Cancer|November 20, 2025
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic PurpuraIlia Spivak, Daniella Magen, Karin Weiss, et al.
Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Journal of Cellular and Molecular Medicine|July 19, 2011
Tight junction proteins expression and modulation in immune cells and multiple sclerosisIlana Mandel, Tamar Paperna, Lea Glass-Marmor, et al.
Familial Cancer|May 17, 2021
A recurrent pathogenic BRCA2 exon 5-11 duplication in the Christian Arab population in IsraelGili Reznick Levi, Gal Larom, Vered Ofen Glassner, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 10, 2012
Multiple sclerosis in diverse populations: characteristics in distinct Arab ethnicities in IsraelMichal Siegel, Tamar Paperna, Izabella Lejbkowicz, et al.
American Journal of Medical Genetics. Part A|June 19, 2021
A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactylyIrena Kessel, Alina German, Amir Peleg, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
European Journal of Medical Genetics|January 9, 2025
A family with an atypical presentation of TBX3-related disorderKhaled Osman, Ayman Asaly, Rana Halloun, et al.
Rambam Maimonides Medical Journal|August 9, 2018
Rare Disease Diagnostics: A Single-center Experience and Lessons LearntKarin Weiss, Alina Kurolap, Tamar Paperna, et al.
Journal of the Neurological Sciences|September 16, 2008
Translation towards personalized medicine in Multiple SclerosisAriel Miller, Nili Avidan, Noa Tzunz-Henig, et al.
European Journal of Medical Genetics|February 7, 2024
Rapid exome sequencing for children with severe acute encephalopathy - A case seriesClair Habib, Tamar Paperna, Rinat Zaid, et al.
Pediatric Blood & Cancer|November 20, 2025
IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic PurpuraIlia Spivak, Daniella Magen, Karin Weiss, et al.
Plos One|April 30, 2013
Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cellsNoa Henig, Nili Avidan, Ilana Mandel, et al.
Journal of Cellular and Molecular Medicine|July 19, 2011
Tight junction proteins expression and modulation in immune cells and multiple sclerosisIlana Mandel, Tamar Paperna, Lea Glass-Marmor, et al.
Familial Cancer|May 17, 2021
A recurrent pathogenic BRCA2 exon 5-11 duplication in the Christian Arab population in IsraelGili Reznick Levi, Gal Larom, Vered Ofen Glassner, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 10, 2012
Multiple sclerosis in diverse populations: characteristics in distinct Arab ethnicities in IsraelMichal Siegel, Tamar Paperna, Izabella Lejbkowicz, et al.
American Journal of Medical Genetics. Part A|June 19, 2021
A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactylyIrena Kessel, Alina German, Amir Peleg, et al.
Pageof 5