Core muscle index is prognostic of survival in advanced ovarian cancers von Conrad, L.B, Awdeh, H, Bailey, A.A, Miller, D, Lea, J.S

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Authors’ reply to ‘Report of extracranial venous stenosis in relapsing–remitting multiple sclerosis patients von Yamout, B, Herlopian, A, Issa, Z, Habib, RH, Fawaz, A, Salame, J, Wadih, A, Awdeh, H, Muallem, N, Raad, R, Al-Kutoubi, A

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Vision-related quality of life in persons with unilateral branch retinal vein occlusion using the 25-item National Eye Institute Visual Function Questionnaire von Awdeh, Richard M, Elsing, Sarah H, Deramo, Vincent A, Stinnett, Sandra, Lee, Paul P, Fekrat, Sharon

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Phototherapeutic Keratectomy for the Treatment of Subepithelial Fibrosis and Anterior Corneal Scarring After Descemet Stripping Automated Endothelial Keratoplasty von Awdeh, Richard M, Abbey, Ashkan M, Vroman, David T, Ying, Michelle S, Goldman, David, Kymionis, George, Yoo, Sonia H

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Extracranial venous stenosis is an unlikely cause of multiple sclerosis von Yamout, Bassem, Herlopian, Aline, Issa, Zeinab, Habib, Robert H, Fawaz, Ahmad, Salame, Joseph, Wadih, Antoine, Awdeh, Haytham, Muallem, Nadime, Raad, Roy, Al-Kutoubi, Aghiab

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Substitution in Arabic: Lisan Al-Arab Dictionary as a Model von Al-Rawashdeh, Basma A.S, Issa, Ahmad H.M. Bani, Rababah, Mahmoud A.I

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Strategies and technical challenges in allele level Class II typing in 2578 bone marrow transplantation donor–recipient pairs von Williams, T.M, Winden, T, Setterholm, M, Vierra-Green, C.A, Spellman, S, Flesch, S, Awdeh, Z, Baxter-Lowe, L.A, Begovich, A.B, Fernandez-Vina, M, Hegland, J, Hurley, C.K, Johnson, D, Noreen, H, Salazar, M, Schmeckpeper, B, Yunis, E.J

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The extent of HLA class II allele level disparity in unrelated bone marrow transplantation : analysis of 1259 National Marrow Donor Program donor-recipient pairs von HURLEY, C. K, BAXTER-LOWE, L. A, YUNIS, E. J, KITAJIMA, D, SHIPP, K, SPLETT, J, WINDEN, T, KOLLMAN, C, JOHNSON, D, NG, J, HARTZMAN, R. J, HEGLAND, J, BEGOVICH, A. B, FERNANDEZ-VINA, M, NOREEN, H, SCHMECKPEPER, B, AWDEH, Z, CHOPCK, M, SALAZAR, M, WILLIAMS, T. M

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Defect in Th1-Like Cells of Nonresponders to Hepatitis B Vaccine von Chedid, Marie G, Deulofeut, Harold, Yunis, David E, Lara-Marquez, Maria Luz, Salazar, Marcela, Deulofeut, Richard, Awdeh, Zuheir, Alper, Chester A, Yunis, Edmond J

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Normal HBsAg presentation and T-cell defect in the immune response of nonresponders von Salazar, M, Deulofeut, H, Granja, C, Deulofeut, R, Yunis, D E, Marcus-Bagley, D, Awdeh, Z, Alper, C A, Yunis, E J

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Extended major histocompatibility complex haplotypes in type I diabetes mellitus von RAUM, D, ZUHEIR AWDEH, YUNIS, E. J, ALPER, C. A, GABBAY, K. H

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MS4 — a high performance output buffering ATM switch von Awdeh, Ra'ed Y, Mouftah, HT

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Two subsets of HLA-DQA1 alleles mark phenotypic variation in levels of insulin autoantibodies in first degree relatives at risk for insulin-dependent diabetes von Pugliese, A, Bugawan, T, Moromisato, R, Awdeh, Z L, Alper, C A, Jackson, R A, Erlich, H A, Eisenbarth, G S

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Cellular recognition and HLA restriction of a midsequence HBsAg peptide in hepatitis B vaccinated individuals von Deulofeut, Harold, Iglesias, Antonio, Mikael, Hagy, Bing, David H., Awdeh, Zuheir, Yunis, Juan, Marcus-Bagley, Deborah, Kruskall, Margot S., Alper, Chester A., Yunis, Edmond J.

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Survey of ATM switch architectures von Awdeh, Ra'ed Y., Mouftah, H.T.

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CD4 TCRBV CDR3 Analysis in prevalent SLE Cases from two ethnic Groups von Fraser, P A, Lu, L-Y, DeCeulaer, K, Schur, P H, Fici, D, Awdeh, Z, Ding, W-Z, Levitan, E, Lew, R, Uko, G, Gonzalez, C

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Improving the performance of delta networks von Awdeh, Ra'ed Y., Mouftah, H.T.

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Statement on the Nomenclature of Human C4 Allotypes von Mauff, G., Alper, C.A., Awdeh, Z., Batchelor, J.R., Bertrams, J., Bruun-Petersen, G., Dawkins, R.L., DéMant, P., Edwards, J., Grosse-Wilde, H., Hauptmann, G., Klouda, P., Lamm, L., Mollenhauer, E., Nerl, C., Olaisen, B., O’Neill, G., Rittner, C., H. Roos, M., Skanes, V., Teisberg, P., Wells, L.

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Genetic analysis of C4 deficiency von Awdeh, Z L, Ochs, H D, Alper, C A

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Complement-human histocompatibility antigen haplotypes in C2 deficiency von Awdeh, Z L, Raum, D D, Glass, D, Agnello, V, Schur, P H, Johnston, Jr, R B, Gelfand, E W, Ballow, M, Yunis, E, Alper, C A

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