Haplotypes among Vietnamese hemoglobin E homozygotes including one with a gamma-globin gene triplication.

Por Nakatsuji, T, Kutlar, A, Kutlar, F, Huisman, T H
Publicado em 1986

Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.

Por Aksoy, M, Kutlar, A, Kutlar, F, Dinçol, G, Erdem, S, Baştesbihçi, S
Publicado em 1985

Postmortem molecular diagnosis of sickle β thalassaemia

Por Kutlar, F, Mirmow, D, Glendenning, M, Holley, L, Kutlar, A
Publicado em 2005

Helicobacter pylori infection in sickle cell disease.

Por Woods, K. F., Onuoha, A., Schade, R. R., Kutlar, A.
Publicado em 2000

The Risks and Benefits of Long-term Use of Hydroxyurea in Sickle Cell Anemia: A 17.5 Year Follow-Up

Por Steinberg, MH, McCarthy, WF, Castro, O, Ballas, SK, Armstrong, FD, Smith, W, Ataga, K, Swerdlow, P, Kutlar, A, DeCastro, L, Waclawiw, MA
Publicado em 2010

Crizanlizumab for the Prevention of Pain Crises in Sickle Cell Disease

Por Ataga, K.I., Kutlar, A., Kanter, J., Liles, D., Cancado, R., Friedrisch, J., Guthrie, T.H., Knight-Madden, J., Alvarez, O.A., Gordeuk, V.R., Gualandro, S., Colella, M.P., Smith, W.R., Rollins, S.A., Stocker, J.W., Rother, R.P.
Publicado no N Engl J Med (2016)