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Baruch Wolach

Showing results (41-50 of 53) with videos related to

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The Israel Medical Association Journal : IMAJ|November 29, 2002
The incidence of primary immunodeficiency syndromes in IsraelHana Golan, Ilan Dalal, Ben-Zion Garty, et al.
Thrombosis and Haemostasis|October 7, 2004
Paediatric cerebral sinus vein thrombosis. A multi-center, case-controlled studyGili Kenet, Dalia Waldman, Aharon Lubetsky, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, 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.
Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, 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.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
The Israel Medical Association Journal : IMAJ|November 29, 2002
The incidence of primary immunodeficiency syndromes in IsraelHana Golan, Ilan Dalal, Ben-Zion Garty, et al.
Thrombosis and Haemostasis|October 7, 2004
Paediatric cerebral sinus vein thrombosis. A multi-center, case-controlled studyGili Kenet, Dalia Waldman, Aharon Lubetsky, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, 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.
Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, 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.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Pageof 6