Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population von Israeli, S., Goldberg, I., Fuchs-Telem, D., Bergman, R., Indelman, M., Bitterman-Deutsch, O., Harel, A., Mashiach, Y., Sarig, O., Sprecher, E.

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Identification of a Novel Locus Associated with Congenital Recessive Ichthyosis on 12p11.2–q13 von Mizrachi-Koren, Mordechai, Geiger, Dan, Indelman, Margarita, Bitterman-Deutsch, Ora, Bergman, Reuven, Sprecher, Eli

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Intravenous Immunoglobulin for Treatment of Toxic Epidermal Necrolysis von Nasser, Maher, Nassar, Faris, Bitterman-Deutsch, Ora

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Impetigo in soldiers after hand-to-hand combat training von Lejbkowicz, Flavio, Samet, Luisa, Belavsky, Larissa, Bitterman-Deutsch, Ora

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Neutral lipid storage disease with ichthyosis: Serum apolipoprotein levels and cholesterol metabolism in monocyte‐derived macrophages von Bergman, R., Aviram, M., Bitterman‐Deutsch, O., Oiknine, Y., Shemer, A., Srebnik, A., Brook, J. G., Friedman‐Birnbaum, R.

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Mal de Meleda keratoderma with pseudoainhum von BKRGMAN, R., BITTERMAN‐DEUTSCH, O., FARTASCH, M., GERSHONI‐BARUCH, R., FRIEDMAN‐BIRNBAUM, R.

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Epidermolysis Bullosa Hereditaria letalis-Herlitz in one of dizygote twins von Bitterman-Deutsch, O., Bergman, R., Falik, Z.

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283 Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a middle eastern population von Mohamad, J., Samuelov, L., Malchin, N., Tiaber, S., Rabinowitz, T., Bitterman-Deutsch, O., Molho-Pessach, V., Cohen-Barak, E., Bach, G., Garty, B., Bergman, R., Harel, A., Nanda, A., Lestringant, G., McGrath, J., Shalev, S., Shomron, N., Mashiach, J., Eskin-Schwartz, M., Sarig, O., Sprecher, E.

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Classic and iatrogenic Kaposi's sarcoma : histopathological patterns as related to clinical course von FRIEDMAN-BIRNBAUM, R, BERGMAN, R, BITTERMAN-DEUTSCH, O, WELTFRIEND, S, LICHTIG, C

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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy von Falik Zaccai, TC, Savitzki, D, Zivony-Elboum, Y, Vilboux, T, Fitts, EC, Shoval, Y, Kalfon, L, Samra, N, Keren, Z, Gross, B, Chasnyk, N, Straussberg, R, Mullikin, JC, Teer, JK, Geiger, D, Kornitzer, D, Bitterman-Deutsch, O, Samson, AO, Wakamiya, M, Peterson, JW, Kirtley, ML, Pinchuk, IV, Baze, WB, Gahl, WA, Kleta, R, Anikster, Y, Chopra, AK

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Mal de Meleda keratoderma with pseudoainhum von BKRGMAN, R., BITTERMAN-DEUTSCH, O., FARTASCH, M., GERSHONI-BARUCH, R., FRIEDMAN-BIRNBAUM, R.

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Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population von Mohamad, Janan, Samuelov, Liat, Malchin, Natalia, Rabinowitz, Tom, Assaf, Sari, Malki, Liron, Malovitski, Kiril, Israeli, Shirli, Grafi‐Cohen, Meital, Bitterman‐Deutsch, Ora, Molho‐Pessach, Vered, Cohen‐Barak, Eran, Bach, Gideon, Garty, Ben Zion, Bergman, Reuven, Harel, Avikam, Nanda, Arti, Lestringant, Giles G., McGrath, John, Shalev, Stavit, Shomron, Noam, Mashiah, Jacob, Eskin‐Schwartz, Marina, Sprecher, Eli, Sarig, Ofer

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Delayed immune mediated adverse effects to hyaluronic acid fillers: report of five cases and review of the literature von Bitterman-Deutsch, Ora, Kogan, Leonid, Nasser, Faris

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A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity von Falik-Zaccai, Tzipora C., Erel-Segal, Reut, Horev, Liran, Bitterman-Deutsch, Ora, Koka, Sivan, Chaim, Sara, Keren, Zohar, Kalfon, Limor, Gross, Bella, Segal, Zvi, Orgal, Shlomi, Shoval, Yishay, Slor, Hanoch, Spivak, Graciela, Hanawalt, Philip C.

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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy von Falik Zaccai, Tzipora C, Savitzki, David, Zivony-Elboum, Yifat, Vilboux, Thierry, Fitts, Eric C, Shoval, Yishay, Kalfon, Limor, Samra, Nadra, Keren, Zohar, Gross, Bella, Chasnyk, Natalia, Straussberg, Rachel, Mullikin, James C, Teer, Jamie K, Geiger, Dan, Kornitzer, Daniel, Bitterman-Deutsch, Ora, Samson, Abraham O, Wakamiya, Maki, Peterson, Johnny W, Kirtley, Michelle L, Pinchuk, Iryna V, Baze, Wallace B, Gahl, William A, Kleta, Robert, Anikster, Yair, Chopra, Ashok K

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Phospholipase A 2 -activating protein is associated with a novel form of leukoencephalopathy von Falik Zaccai, Tzipora C., Savitzki, David, Zivony-Elboum, Yifat, Vilboux, Thierry, Fitts, Eric C., Shoval, Yishay, Kalfon, Limor, Samra, Nadra, Keren, Zohar, Gross, Bella, Chasnyk, Natalia, Straussberg, Rachel, Mullikin, James C., Teer, Jamie K., Geiger, Dan, Kornitzer, Daniel, Bitterman-Deutsch, Ora, Samson, Abraham O., Wakamiya, Maki, Peterson, Johnny W., Kirtley, Michelle L., Pinchuk, Iryna V., Baze, Wallace B., Gahl, William A., Kleta, Robert, Anikster, Yair, Chopra, Ashok K.

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Chanarin–Dorfman syndrome: Deficiency in CGI-58, a lipid droplet-bound coactivator of lipase von Yamaguchi, Tomohiro, Osumi, Takashi

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Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population von Macriz-Romero, Nicole, Vera-Duarte, Guillermo Raul, Guerrero-Becerril, Jesus, Chacón-Camacho, Oscar Francisco, Astiazarán, Mirena C, Zenteno, Juan Carlos, Graue-Hernandez, Enrique O.

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A New Anti-loxoscelic Serum Produced Against Recombinant Sphingomyelinase D: Results of Preclinical Trials von de Almeida, Daniel Manzoni, Fernandes-Pedrosa, Matheus de F, de Andrade, Rute M. Goncalves, Marcelino, Jose Roberto, Gondo-Higashi, Hisako, de Azevedo, Inacio de L. M. Junqueira, Ho, Paulo Lee, van den Berg, Carmen, Tambourgi, Denise V

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A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda von Muslumanoglu, M.H., Saracoglu, N., Cilingir, O., Basmaci, T., Urer, S., Sabuncu, I., Demir, S., Bademci, G., Artan, S.

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