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Ronit Gavrieli

Showing results (21-30 of 27) with videos related to

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Clinical Immunology (Orlando, Fla.)|August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Blood Cells, Molecules & Diseases|October 14, 2015
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi JewsMartin de Boer, Shay Tzur, Karin van Leeuwen, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Journal of Medical Genetics|January 15, 2018
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi JewsMartin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
The Journal of Experimental Medicine|November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsAtar Lev, Yu Nee Lee, Guangping Sun, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Clinical Immunology (Orlando, Fla.)|August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Blood Cells, Molecules & Diseases|October 14, 2015
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi JewsMartin de Boer, Shay Tzur, Karin van Leeuwen, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Journal of Medical Genetics|January 15, 2018
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi JewsMartin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
The Journal of Experimental Medicine|November 24, 2020
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defectsAtar Lev, Yu Nee Lee, Guangping Sun, et al.
The New England Journal of Medicine|June 7, 2013
A congenital neutrophil defect syndrome associated with mutations in VPS45Thierry Vilboux, Atar Lev, May Christine V Malicdan, et al.
Pageof 3