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Results: 1-14 |
Results: 14

Authors: Barbeau, P Woods, KF Ramsey, LT Litaker, MS Pollock, DM Pollock, JS Callahan, LA Kutlar, A Mensah, GA Gutin, B
Citation: P. Barbeau et al., Exercise in sickle cell anemia: Effect on inflammatory and vasoactive mediators, ENDOTHELIU, 8(2), 2001, pp. 147-155

Authors: Kutlar, A
Citation: A. Kutlar, Proceedings of the Titus H. J. Huisman Memorial Symposium - Welcome, HEMOGLOBIN, 25(2), 2001, pp. 117-118

Authors: Kutlar, A Kutlar, F Turker, I Tural, C
Citation: A. Kutlar et al., The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease, HEMOGLOBIN, 25(2), 2001, pp. 213-217

Authors: Adekile, AD Kutlar, F Haider, MZ Kutlar, A
Citation: Ad. Adekile et al., Frequency of the 677 C -> T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients, AM J HEMAT, 66(4), 2001, pp. 263-266

Authors: Orringer, EP Casella, JF Ataga, KI Koshy, M Adams-Graves, P Luchtman-Jones, L Wun, T Watanabe, M Shafer, F Kutlar, A Abboud, M Steinberg, M Adler, B Swerdlow, P Terregino, C Saccente, S Files, B Ballas, S Brown, R Wojtowicz-Praga, S Grindel, JM
Citation: Ep. Orringer et al., Purified poloxamer 188 for treatment of acute vaso-occlusive crisis of sickle cell disease - A randomized controlled trial, J AM MED A, 286(17), 2001, pp. 2099-2106

Authors: Araten, DJ Swirsky, D Karadimitris, A Notaro, R Nafa, K Bessler, M Thaler, HT Castro-Malaspina, H Childs, BH Boulad, F Weiss, M Anagnostopoulos, N Kutlar, A Savage, DG Maziarz, RT Jhanwar, S Luzzatto, L
Citation: Dj. Araten et al., Cytogenetic and morphological abnormalities in paroxysmal nocturnal haemoglobinuria, BR J HAEM, 115(2), 2001, pp. 360-368

Authors: Woods, KF Johnson, JA Kutlar, A Daitch, L Stachura, ME
Citation: Kf. Woods et al., Sickle cell disease telemedicine network for rural outreach, J TELEMED T, 6(5), 2000, pp. 285-290

Authors: Valafar, H Valafar, F Darvill, A Albersheim, P Kutlar, A Woods, KF Hardin, J
Citation: H. Valafar et al., Predicting the effectiveness of hydroxyurea in individual sickle cell anemia patients, ARTIF INT M, 18(2), 2000, pp. 133-148

Authors: Jillella, AP Kallab, AM Kutlar, A
Citation: Ap. Jillella et al., Autoimmune thrombocytopenia following autologous hematopoietic cell transplantation: review of literature and treatment options, BONE MAR TR, 26(8), 2000, pp. 925-927

Authors: Woods, KF Onuoha, A Schade, RR Kutlar, A
Citation: Kf. Woods et al., Helicobacter pylori infection in sickle cell disease, J NAT MED A, 92(7), 2000, pp. 361-365

Authors: Woods, KF Kutlar, A Johnson, JA Waller, JL Grigsby, RK Stachura, ME Rahn, DW
Citation: Kf. Woods et al., Sickle cell telemedicine and standard clinical encounters: A comparison ofpatient satisfaction, TELEMED J, 5(4), 1999, pp. 349-356

Authors: Tadmouri, GO Bilenoglu, O Kutlar, F Markowitz, RB Kutlar, A Basak, AN
Citation: Go. Tadmouri et al., Identification of the Chinese IVS-II-654 (C -> T) beta-thalassemia mutation in an immigrant Turkish family: Recurrence or migration?, HUMAN BIOL, 71(2), 1999, pp. 295-302

Authors: Woods, K Kutlar, A Grigsby, RK Adams, L Stachura, ME
Citation: K. Woods et al., Primary-care delivery for sickle cell patients in rural Georgia using telemedicine, TELEMED J, 4(4), 1998, pp. 353-361

Authors: Tuohy, AMM McKie, VC Sabio, H Kutlar, F Kutlar, A Wilson, JB
Citation: Amm. Tuohy et al., Hb Hammersmith [beta 42(CD1)Phe -> Ser]: Occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies, J PED H ONC, 20(6), 1998, pp. 563-566
Risultati: 1-14 |