C0328: Analysis of the Complement Pathway Mutations in Atypical Hemolytic Uremic Syndrome (AHUS) by Sabri Hancer, V, Guvenc, S, Hindilerden, F, Buyukdogan, M, Diz-Kucukkaya, R

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T‐cell‐rich B‐cell lymphoma of the spleen presenting with severe hypersplenism by DINCOL, G., AGAN, M., DOGAN, O., DIZ‐KUCUKKAYA, R., USLU, B.

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Antiphospholipid antibodies and antiphospholipid syndrome in patients presenting with immune thrombocytopenic purpura: a prospective cohort study by Diz-Küçükkaya, Reyhan, Hacıhanefioǧlu, Abdullah, Yenerel, Mustafa, Turgut, Mehmet, Keskin, Hüseyin, Nalçacı, Meliha, l˙nanç, Murat

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Development of hairy cell leukemia in a patient with antiphospholipid syndrome by Diz-Kucukkaya, R., Dincol, G., Kamali, S., Kural, F., Inanc, M.

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Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region by Afshar-Kharghan, Vahid, Diz-Küçükkaya, Reyhan, Ludwig, Erwin H., Marian, Ali J., López, José A.

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Assessment of cardiac structure and left atrial appendage functions in primary antiphospholipid syndrome: A transesophageal echocardiographic study by ERDOGAN, Dogan, GOREN, M. Taner, DIZ-KUCUKKAYA, Reyhan, INANC, Murat

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P-selectin glycoprotein ligand-1 VNTR polymorphisms and risk of thrombosis in the antiphospholipid syndrome by Diz-Kucukkaya, Reyhan, Inanc, Murat, Afshar-Kharghan, Vahid, Zhang, Q Ed, López, José A, Pekcelen, Yuksel

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The Association Between Factor XIII Val34Leu Polymorphism and Early Myocardial Infarction by Hancer, Veysel Sabri, Diz-Kucukkaya, Reyhan, Bilge, Ahmet Kaya, Ozben, Beste, Oncul, Aytac, Ergen, Gursel, Nalcaci, Meliha

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Bullous acral erythema and concomitant pigmentation on the face and occluded skin by Özkaya-Bayazit, Esen, Diz-Küçükkaya, Reyhan, Akasya, Esra, Büyükbabani, Nesimi, Öncü, Şeref, Pekçelen, Yüksel

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Cytoplasmic Truncation of Glycoprotein Ibα Weakens Its Interaction with von Willebrand Factor and Impairs Cell Adhesion by Schade, Alicia J, Arya, Maneesh, Gao, Shan, Diz-Küçükkaya, Reyhan, Anvari, Bahman, McIntire, Larry V, López, José A, Dong, Jing-fei

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Factor XIII Val34Leu polymorphism does not contribute to the prevention of thrombotic complications in patients with antiphospholipid syndrome by Diz-Kucukkaya, R, Hancer, V S, Inanc, M, Nalcaci, M, Pekcelen, Y

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Turkish population data on the factor XIII Val34Leu,glycoprotein (GP)Ibα Kozak and P-selectin glycoprotein ligand 1 (PSGL-1) loci by Hancer, Veysel Sabri, Diz-Kucukkaya, Reyhan, Nalcaci, Meliha

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Paroxysmal nocturnal hemoglobinuria clone in patients with myelodysplastic syndrome by Yenerel, Mustafa N., Diz‐Kucukkaya, Reyhan, Besisik, Sevgi, Aktan, Melih, Nalcaci, Meliha, Dincol, Günçag, Hacihanefioglu, Abdullah, Turgut, Mehmet

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Coexistence of homozygous factor V Leiden mutation and antiphospholipid antibodies in two patients presented with Budd-Chiari syndrome by Nalcaci, Meliha, Yenerel, Mustafan, Inanc, Murat, Demir, Kadir, Kaymakoglu, Sabahattin, Diz-Kucukkaya, Reyhan

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CASE REPORT: T-cell-rich B-cell lymphoma of the spleen presenting with severe hypersplenism by Dincol, G, Agan, M, Dogan, O, Diz-Kucukkaya, R, Uslu, B

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OP-043: POLYMORPHISMS OF THE ANGIOTENSIN CONVERTING ENZYME AND ANGIOTENSINOGEN GENE IN PATIENTS WITH ATRIAL FIBRILLATION by Topal, N. Papila, Ozben, B, Hancer, V.S, Tanrikulu, A.M, Kucukkaya, R. Diz, Fak, A.S, Erdogan, O, Basaran, Y, Yesildag, O

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Development of a New International Antiphospholipid Syndrome Classification Criteria Phase I/II Report: Generation and Reduction of Candidate Criteria by Barbhaiya, Medha, Zuily, Stephane, Ahmadzadeh, Yasaman, Amigo, Mary‐Carmen, Avcin, Tadej, Bertolaccini, Maria Laura, Branch, D. Ware, Jesus, Guilherme, Devreese, Katrien M. J., Frances, Camille, Garcia, David, Guillemin, Francis, Levine, Steven R., Levy, Roger A., Lockshin, Michael D., Ortel, Thomas L., Seshan, Surya V., Tektonidou, Maria, Wahl, Denis, Willis, Rohan, Naden, Ray, Costenbader, Karen, Erkan, Doruk, Agmon‐Levin, Nancy, Aguilar, Cassyanne, Alba, Paula, Alpan, Oral, Ambrozic, Ales, Amoura, Zahir, Andrade, Danieli, Andrade, Luis, Appenzeller, Simone, Esen, Bahar Artim, Atsumi, Tatsuya, Berkun, Yackov, Cabral, Antonio, Canaud, Guillaume, Cervera, Ricard, Chen, Pojen, Chighizola, Cecilia, Cimaz, Rolando, Cohen, Hannah, Costedoat‐Chalumeau, Nathalie, Crowther, Mark, Cuadrado, Maria Jose, de Groot, Philip G., de Moerloose, Philippe, Derksen, Ronald, Diz‐Kucukkaya, Reyhan, Dörner, Thomas, Fortin, Paul, Giannakopoulos, Bill, Gómez‐Puerta, Jose A., Gonzalez, Emilio B., Inanc, Murat, Kenet, Gili, Khamashta, Munther, Kriegel, Martin, Krilis, Steven, Laskin, Carl, Massicotte, Patti, McCarty, Gale, Meroni, Pier Luigi, Mikdashi, Jamal, Myones, Barry, Pengo, Vittorio, Petri, Michelle, Roubey, Robert, Sammaritano, Lisa, Sanna, Giovanni, Sciascia, Savino, Signorelli, Flavio, Soybilgic, Arzu, Tincani, Angela, Woller, Scott, Yelnik, Cécile

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T-cell-rich B-cell lymphoma of the spleen presenting with severe hypersplenism by DINCOL, G., AGAN, M., DOGAN, O., DIZ-KUCUKKAYA, R., USLU, B.

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The 2023 ACR / EULAR Antiphospholipid Syndrome Classification Criteria by Barbhaiya, Medha, Zuily, Stephane, Naden, Ray, Hendry, Alison, Manneville, Florian, Amigo, Mary‐Carmen, Amoura, Zahir, Andrade, Danieli, Andreoli, Laura, Artim‐Esen, Bahar, Atsumi, Tatsuya, Avcin, Tadej, Belmont, H. Michael, Bertolaccini, Maria Laura, Branch, D. Ware, Carvalheiras, Graziela, Casini, Alessandro, Cervera, Ricard, Cohen, Hannah, Costedoat‐Chalumeau, Nathalie, Crowther, Mark, de Jesus, Guilherme, Delluc, Aurelien, Desai, Sheetal, De Sancho, Maria, Devreese, Katrien M., Diz‐Kucukkaya, Reyhan, Duarte‐Garcia, Ali, Frances, Camille, Garcia, David, Gris, Jean‐Christophe, Jordan, Natasha, Leaf, Rebecca K., Kello, Nina, Knight, Jason S., Laskin, Carl, Lee, Alfred I., Legault, Kimberly, Levine, Steve R., Levy, Roger A., Limper, Maarten, Lockshin, Michael D., Mayer‐Pickel, Karoline, Musial, Jack, Meroni, Pier Luigi, Orsolini, Giovanni, Ortel, Thomas L., Pengo, Vittorio, Petri, Michelle, Pons‐Estel, Guillermo, Gomez‐Puerta, Jose A., Raimboug, Quentin, Roubey, Robert, Sanna, Giovanni, Seshan, Surya V., Sciascia, Savino, Tektonidou, Maria G., Tincani, Angela, Wahl, Denis, Willis, Rohan, Yelnik, Cecile, Zuily, Catherine, Guillemin, Francis, Costenbader, Karen, Erkan, Doruk

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Genotoxicity and sister chromatid exchange in patients with myelodysplastic disorders by Öztürk, Şükrü, Palanduz, Şükrü, Çefle, Kıvanç, Tutkan, Gülçin, Uçur, Ali, Dinçol, Günçağ, Nalçacı, Meliha, Aktan, Melih, Yavuz, Selim, Küçükkaya, Reyhan Diz

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