Hb M Dothan [β 25/26 (B7/B8)/(GGT/GAG→GAG//Gly/Glu→Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics von Kutlar, F., Hilliard, L.M., Zhuang, L., Patel, N., Eroglu, B., Meiler, S.E., Carmichael, H., Russell, R.B., Kutlar, A.

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Pomalidomide augments fetal hemoglobin production without the myelosuppressive effects of hydroxyurea in transgenic sickle cell mice von Meiler, Steffen E., Wade, Marlene, Kutlar, Ferdane, Yerigenahally, Shobha D., Xue, Yongjun, Moutouh-de Parseval, Laure A., Corral, Laura G., Swerdlow, Paul S., Kutlar, Abdullah

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The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state s... von Adekile, A, Kutlar, F, McKie, K, Addington, A, Elam, D, Holley, L, Clair, B, Kutlar, A

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Postmortem molecular diagnosis of sickle β thalassaemia von Kutlar, F, Mirmow, D, Glendenning, M, Holley, L, Kutlar, A

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THE METHYLENE TETRAHYDROFOLATE REDUCTASE (C677T) MUTATION AS A POTENTIAL RISK FACTOR FOR AVASCULAR NECROSIS IN SICKLE CELL DISEASE von Kutlar, Abdullah, Kutlar, Ferdane, Turker, Ibrahim, Tural, Canan

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Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography von Adams, Robert J, McKie, Virgil C, Hsu, Lewis, Files, Beatrice, Vichinsky, Elliott, Pegelow, Charles, Abboud, Miguel, Gallagher, Dianne, Kutlar, Abdullah, Nichols, Fenwick T, Bonds, Duane R, Brambilla, Donald, Woods, Gerald, Olivieri, Nancy, Driscoll, Catherine, Miller, Scott, Wang, Winfred, Hurlett, Anne, Scher, Charles, Berman, Brian, Carl, Elizabeth, Jones, Anne M, Roach, E. Steve, Wright, Elizabeth, Zimmerman, Robert A, Waclawiw, Myron

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Frequency of the 677 C→T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients von Adekile, A.D., Kutlar, F., Haider, M.Z., Kutlar, A.

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Separation of normal and abnormal hemoglobin chains by reversed-phase high-performance liquid chromatography von Kutlar, F, Kutlar, A, Huisman, T.H.J

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Recurrent and Progressive Abdominal Pain and Enteritis in a Japanese Patient with Paroxysmal Nocturnal Hemoglobinuria von Hino, Akihisa, Yamashita, Yukiko, Yamaguchi, Mitsuhiro, Azenishi, Yasuhiko

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Clinical and Genetic Heterogeneity in Black Patients With Homozygous β-Thalassemia From the Southeastern United States von Gonzalez-Redondo, J.M., Stoming, T.A., Lanclos, K.D., Gu, Y.C., Kutlar, A., Kutlar, F., Nakatsuji, T., Deng, B., Han, I.S., McKie, V.C., Huisman, T.H.J.

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A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia von Gonzalez-Redondo, JM, Stoming, TA, Kutlar, A, Kutlar, F, Lanclos, KD, Howard, EF, Fei, YJ, Aksoy, M, Altay, C, Gurgey, A

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An α-2 Globin Gene Initiation Codon Mutation in a Vietnamese Patient with Hb H Disease von KUTLAR, F., ADAMKIEWICZ, T. V., MARKOWITZ, R. B., HOLLEY, L., KUTLAR, A.

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Successful Outcome of Chronic Intrahepatic Cholestasis in an Adult Patient with Sickle Cell/β+ Thalassemia von Vlachaki, Euthymia, Boura, Panagiota, Katsinelos, Panagiotis, Vetsiou, Evaggelia, Andreadis, Panagiotis, Neokleous, Nikolaos, Agapidou, Aleka

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A New Sickling Variant ‘Hb S-Wake β[(Glu6Val-Asn139 Ser)]’ Found in a Compound Heterozygote with Hb S β(Glu6Val) Coinherited with Homozygous α-Thalassemia-2: Phenotype and Molecula... von Kutlar, F., Redding-Lallinger, R., Meiler, S.E., Bakanay, S.M., Borders, L., Kutlar, A.

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Bendamustine Associated with Irreversible Ascending Paralysis von Alhafez, Ashraf, Aljitawi, Omar S., Lin, Tara L., Ganguly, Siddhartha, Abhyankar, Sunil, McGuirk, Joseph P.

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Mild and Severe β-Thalassemia Among Homozygotes From Turkey: Identification of the Types by Hybridization of Amplified DNA With Synthetic Probes von Diaz-Chico, J.C., Yang, K.G., Stoming, T.A., Efremov, D.G., Kutlar, A., Kutlar, F., Aksoy, M., Altay, C., Gurgey, A., Kilinc, Y., Huisman, T.H.J.

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Postmortem molecular diagnosis of sickle [beta] thalassaemia von Kutlar, F, Mirmow, D, Glendenning, M, Holley, L, Kutlar, A

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Postmortem molecular diagnosis of sickle β thalassaemia: Figure 1 von Kutlar, F, Mirmow, D, Glendenning, M, Holley, L, Kutlar, A

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Missense mutation of the last nucleotide of exon 1 (G->C) of globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wil... von Agarwal, Neeraj, Kutlar, Ferdane, Mojica-Henshaw, Mariluz P, Ou, Ching N, Gaikwad, Amos, Reading, N. Scott, Bailey, Lakeia, Kutlar, Abdullah, Prchal, Josef T

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Molecular characterization of Hb S(C) β‐thalassemia in American blacks von Gonzalez‐Redondo, J. M., Kutlar, A., Kutlar, F., McKie, V. C., McKie, K. M., Baysal, E., Huisman, T. H. J.

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