Multiple nodular fasciitis presenting initially as a chest wall tumor von Banjer, A H, Abaza, M A, Al-Fattani, M O, Ezzeldin, K L

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Abstract 059: 2023 Highlights from the Prospective CASSH Registry von Ezzeldin, M., Delora, A., Martucci, M., Kahathuduwa, C. N., Hassan, A. E., Hussain, M. S., Miller, S., Chaubal, V., Ezzeldin, R., Mealer, L., Grandhi, R., Sheriff, F., Tanweer, O., Alaraj, A., Niazi, M., Bushnaq, S., Asif, K., Salah, W., Rodriguez, G., Maud, A., Shaikh, S., Navpreet, B., Bhatti, I., AlMajali, M., Abou-mrad, T., Nico, E., Quispe-Orozco, D., Abdulrazzak, M. A., Froukh, M., Zaidat, O., Siddiq, F.

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Methylation of the DPYD Promoter: An Alternative Mechanism for Dihydropyrimidine Dehydrogenase Deficiency in Cancer Patients von EZZELDIN, Hany H, LEE, Adam M, MATTISON, Lori K, DIASIO, Robert B

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Elevated serum tumour necrosis factor‐like weak inducer of apoptosis in alopecia areata: a possible marker of disease severity von Sayed, K., Mohammed, F., Abdel Hay, R., Ezzeldin, N., Rashed, L., Fahim, A.

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Genetic regulation of dihydropyrimidinase and its possible implication in altered uracil catabolism von Thomas, Holly R, Ezzeldin, Hany H, Guarcello, Vincenzo, Mattison, Lori K, Fridley, Brooke L, Diasio, Robert B

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Genetic regulation of β-ureidopropionase and its possible implication in altered uracil catabolism von Thomas, Holly R, Ezzeldin, Hany H, Guarcello, Vincenzo, Mattison, Lori K, Fridley, Brooke L, Diasio, Robert B

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Right-sided maze procedure for atrial tachyarrhythmias in congenital heart disease. Discussion von STULAK, John M, DEARANI, Joseph A, PUGA, Francisco J, ZEHR, Kenton J, SCHAFF, Hartzell V, DANIELSON, Gordon K, MOSTAFA, Ezzeldin A

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Localized non-Hodgkin's lymphoma of Waldeyer's ring: Clinical features, management, and prognosis of 130 adult patients von Ezzat, Adnan A., Ibrahim, Ezzeldin M., El Weshi, Amr N., Khafaga, Yasser M., AlJurf, Mahmoud, Martin, Justin M., Ajarim, Dahish S., Bazarbashi, Shouki N., Stuart, Robert K., Zucca, Emanuele

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Dihydropyrimidine dehydrogenase deficiency (DPD) in GI malignancies: Experience of 4 years von Mehra, R., Mattison, L. K., Ledbetter, L., Ezzeldin, H., Diasio, R. B., Saif, M. W.

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Molecular basis of altered uracil catabolism in individuals with 5-FU toxicity and normal DPD enzyme activity von Reed, H. A., Ezzeldin, H. H., Mattison, L. K., Diasio, R. B.

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Genetic regulation of ss-ureidopropionase and its possible implication in altered uracil catabolism von THOMAS, Holly R, EZZELDIN, Hany H, GUARCELLO, Vincenzo, MATTISON, Lori K, FRIDLEY, Brooke L, DIASIO, Robert B

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Evidence for increased incidence of dihydropyrimidine dehydrogenase (DPD) deficiency in African Americans compared to Caucasians von Mattison, L. K., Fourie, J., Carpenter, M., Ezzeldin, H., Johnson, M. R., Saif, M., Modak, A., Diasio, R. B.

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High complete pathological response in locally advanced breast cancer using paclitaxel and cisplatin von EZZAT, Adnan A, IBRAHIM, Ezzeldin M, AJARIM, Dahish S, RAHAL, Mohammed M, RAJA, Madras A, STUART, Robert K, TULBAH, Asma M, KANDIL, Alaa, AL-MALIK, Osama A, BAZARBASHI, Shouki M

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Breast cancer in the Eastern Province of Saudi Arabia von IBRAHIM, E. M, AL-MULHIM, F. A, AL-AMRI, A, AL-MUHANNA, F. A, EZZAT, A. A, STUART, R. K, AJARIM, D

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The correlation between prostate volume, transition zone volume, transition zone index and clinical and urodynamic investigations in patients with lower urinary tract symptoms von WITJES, W.P.J., AARNINK, R.G., EZZ‐EL‐DIN, K., WIJKSTRA, H., DEBRUYNE, F.M.J., De La ROSETTE, J.J.M.C.H.

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Electroretinographic Abnormalities in Parents of Patients With Leber Congenital Amaurosis Who Have Heterozygous GUCY2D Mutations von Koenekoop, Robert K, Fishman, Gerald A, Iannaccone, Alessandro, Ezzeldin, Hany, Ciccarelli, Maria L, Baldi, Alfonso, Sunness, Janet S, Lotery, Andrew J, Jablonski, Monica M, Pittler, Steven J, Maumenee, Irene

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