未登录Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Lev, Atar; Lee, Yu Nee; Sun, Guangping; Hallumi, Enas; Simon, Amos J.; Zrihen, Keren S.; Levy, Shiran; Halevi, Tal Beit; Papazian, Maria; Shwartz, Neta; Somekh, Ido; Levy-Mendelovich, Sarina; Wolach, Baruch; Gavrieli, Ronit; Vernitsky, Helly; Barel, Ortal; Javasky, Elisheva; Stauber, Tali; Ma, Chi A.; Zhang, Yuan; Amariglio, Ninette; Rechavi, Gideon; Hendel, Ayal; Yablonski, Deborah; Milner, Joshua D.; Somech, Raz
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收藏Leucocyte adhesion deficiency-A multicentre national experience
Wolach, Baruch; Gavrieli, Ronit; Wolach, Ofir; Stauber, Tal; Abuzaitoun, Omar; Kuperman, Amir; Amir, Yaakov; Stepensky, Polina; Somech, Raz; Etzioni, Amos
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收藏Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)
Wolach, Baruch; Gavrieli, Ronit; de Boer, Martin; van Leeuwen, Karin; Wolach, Ofir; Grisaru-Soen, Galia; Broides, Arnon; Etzioni, Amos; Somech, Raz; Roos, Dirk
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收藏A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews
De Boer, Martin; Gavrieli, Ronit; van Leeuwen, Karin; Wolf, Haike Reznik; Dushnitzki, Maya; Bar-Yosef, Yifaat; Bar-Ziv, Anat; Behar, Doron; Lipitz, Shlomo; Miller, Tal Elkan; Tool, Anton T. J.; Kuijpers, Taco W.; van den Berg, Timo K.; Wolach, Baruch; Roos, Dirk; Pras, Elon
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收藏Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients
Wolach, Baruch; Gavrieli, Ronit; de Boer, Martin; van Leeuwen, Karin; Berger-Achituv, Sivan; Stauber, Tal; Ben Ari, Josef; Rottem, Menachem; Schlesinger, Yechiel; Grisaru-Soen, Galia; Abuzaitoun, Omar; Marcus, Nufar; Garty, Ben Zion; Broides, Arnon; Levy, Jakov; Stepansky, Polina; Etzioni, Amos; Somech, Raz; Roos, Dirk
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收藏A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45
Vilboux, Thierry; Lev, Atar; Malicdan, May Christine V.; Simon, Amos J.; Jaervinen, Paeivi; Racek, Tomas; Puchalka, Jacek; Sood, Raman; Carrington, Blake; Bishop, Kevin; Mullikin, James; Huizing, Marjan; Garty, Ben Zion; Eyal, Eran; Wolach, Baruch; Gavrieli, Ronit; Toren, Amos; Soudack, Michalle; Atawneh, Osama M.; Babushkin, Tatiana; Schiby, Ginette; Cullinane, Andrew; Avivi, Camila; Polak-Charcon, Sylvie; Barshack, Iris; Amariglio, Ninette; Rechavi, Gideon; ten Bosch, Jutte van der Werff; Anikster, Yair; Klein, Christoph; Gahl, William A.; Somech, Raz
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收藏Chronic granulomatous disease of childhood: an unusual cause of recurrent uncommon infections in a 61-year-old man
Isman-Nelkenbaum, G.; Wolach, B.; Gavrieli, R.; Roos, D.; Sprecher, E.; Bash, E.; Gat, A.; Sprecher, H.; Ben-Ami, R.; Zeeli, T.
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收藏Cytosolic Phospholipase A2α Is Targeted to the p47phox-PX Domain of the Assembled NADPH Oxidase via a Novel Binding Site in Its C2 Domain
Shmelzer, Zeev; Karter, Maria; Eisenstein, Miriam; Leto, Thomas L.; Hadad, Nurit; Ben-Menahem, David; Gitler, Daniel; Banani, Shirly; Wolach, Baruch; Rotem, Meir; Levy, Rachel
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收藏Chronic granutomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase
Roos, Dirk; de Boer, Martin; Koker, M. Yavuz; Dekker, Jan; Singh-Gupta, Vinita; Ahlin, Anders; Palmblad, Jan; Sanal, Ozden; Kurenko-Deptuch, Magdalena; Jolles, Stephen; Wolach, Baruch
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