Cellular and clinical report of new Griscelli syndrome type III cases von Westbroek, Wendy, Klar, Aharon, Cullinane, Andrew R., Ziegler, Shira G., Hurvitz, Haggit, Ganem, Ashraf, Wilson, Kirkland, Dorward, Heidi, Huizing, Marjan, Tamimi, Haled, Vainshtein, Igor, Berkun, Yackov, Lavie, Moran, Gahl, William A., Anikster, Yair

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Two novel mutations identified in familial cases with Donohue syndrome von Falik Zaccai, Tzipora C., Kalfon, Limor, Klar, Aharon, Elisha, Mordechai Ben, Hurvitz, Haggit, Weingarten, Galina, Chechik, Emelia, Fleisher Sheffer, Vered, Haj Yahya, Raid, Meidan, Gal, Gross‐Kieselstein, Eva, Bauman, Dvora, Hershkovitz, Sylvia, Yaron, Yuval, Orr‐Urtreger, Avi, Wertheimer, Efrat

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If von Schenk, Barbara, Imbach, Timo, Frank, Christian G., Grubenmann, Claudia E., Raymond, Gerald V., Hurvitz, Haggit, Raas-Rotschild, Annick, Luder, Anthony S., Jaeken, Jaak, Berger, Eric G., Matthijs, Gert, Hennet, Thierry, Aebi, Markus

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Prolidase deficiency: it looks like systemic lupus erythematosus but it is not von Klar, Aharon, Navon-Elkan, Paulina, Rubinow, Alan, Branski, David, Hurvitz, Haggit, Christensen, Ernst, Khayat, Morad, Falik-Zaccai, Tzipora C.

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Treatment with hypertonic saline versus normal saline nasal wash of pediatric chronic sinusitis von Shoseyov, David, Bibi, Haim, Shai, Pintov, Shoseyov, Nurit, Shazberg, Gila, Hurvitz, Haggit

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If von Schenk, B, Imbach, T, Frank, C G, Grubenmann, C E, Raymond, G V, Hurvitz, H, Korn-Lubetzki, I, Revel-Vik, S, Raas-Rotschild, A, Luder, A S, Jaeken, J, Berger, E G, Matthijs, G, Hennet, T, Aebi, M

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Evidence that Griscelli Syndrome with Neurological Involvement Is Caused by Mutations in RAB27A, Not MYO5A von Anikster, Yair, Huizing, Marjan, Anderson, Paul D., Fitzpatrick, Diana L., Klar, Aharon, Gross-Kieselstein, Eva, Berkun, Yackov, Shazberg, Gila, Gahl, William A., Hurvitz, Haggit

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Atrial natriuretic peptide in children with pneumonia von Haviv, Michal, Haver, Eitan, Lichtstein, David, Hurvitz, Haggit, Klar, Aharon

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Sludge Ball, Pseudolithiasis, Cholelithiasis and Choledocholithiasis from Intrauterine Life to 2 Years: A 13‐Year Follow‐Up von Klar, Aharon, Branski, David, Akerman, Yaacov, Nadjari, Michael, Berkun, Yaacov, Moise, Jonathan, Shazberg, Gila, Revel‐Vilk, Shoshana, Israeli, Talia, Katz, Gabriel, Levy, Arie, Ami, Anat Ben, Hurvitz, Haggit

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Kingella kingae endocarditis and sepsis in an infant von BERKUN, Yackov, BRAND, Abraham, KLAR, Aharon, HALPERIN, Efraim, HURVITZ, Haggit

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Mutation analysis of the FAH gene in Israeli patients with tyrosinemia type I von Elpeleg, Orly N., Shaag, Avraham, Holme, Elizabeth, Zughayar, Ghaleb, Ronen, Suzi, Fisher, Drora, Hurvitz, Haggit

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Early peripheral nervous system manifestations of infantile Krabbe disease von Korn-Lubetzki, Isabelle, Dor-Wollman, Talia, Soffer, Dov, Raas-Rothschild, Annick, Hurvitz, Haggit, Nevo, Yoram

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Recurrent Acute Disseminated Encephalomyelitis Associated With Acute Cytomegalovirus and Epstein-Barr Virus Infection von Revel-Vilk, Shoshana, Hurvitz, Haggit, Klar, Aharon, Virozov, Yelena, Kom-Lubetzki, Isabelle

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Intestinal Protein Loss and Hypoalbuminemia in Children with Pneumonia von Klar, Aharon, Shoseyov, David, Berkun, Yaakov, Brand, Abraham, Braun, Jacques, Shazberg, Gila, Jonathan, Moise, Gross-Kieselstein, Eva, Revel-Vilk, Shoshana, Hurvitz, Haggit

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The clinical course of bronchiolitis associated with acute otitis media von Shazberg, Gila, Revel-Vilk, Shoshana, Shoseyov, David, Ben-Ami, Anat, Klar, Aharon, Hurvitz, Haggit

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Intestinal Protein Loss and Hypoalbuminemia in Children with Pneumonia von Klar, Aharon, Shoseyov, David, Berkun, Yaakov, Brand, Abraham, Braun, Jacques, Shazberg, Gila, Jonathan, Moise, Gross‐Kieselstein, Eva, Revel‐Vilk, Shoshana, Hurvitz, Haggit

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If von Schenk, Barbara, Imbach, Timo, Frank, Christian G., Grubenmann, Claudia E., Raymond, Gerald V., Hurvitz, Haggit, Raas-Rotschild, Annick, Luder, Anthony S., Jaeken, Jaak, Berger, Eric G., Matthijs, Gert, Hennet, Thierry, Aebi, Markus

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If von Schenk, B.

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Evidence that griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYOSA von ANIKSTER, Yair, HUIZING, Marjan, ANDERSON, Paul D, FITZPATRICK, Diana L, KLAR, Aharon, GROSS-KIESELSTEIN, Eva, BERKUN, Yackov, SHAZBERG, Gila, GAHL, William A, HURVITZ, Haggit

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Recurrent acute disseminated encephalomyelities associated with acute cytomegalovirus and Epstein-Barr virus infection von Revel-Vilk, Shoshanan, Hurvitz, Haggit, Klar, Aharon, Virozov, Yelena, Korn-Lubetzki, Isabelle

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