Harmatz P - Search Results

1

Comparison of organ dysfunction in transfused patients with SCD or beta thalassemia.

Vichinsky E, Butensky E, Fung E, Hudes M, Theil E, Ferrell L, Williams R, Louie L, Lee PD, Harmatz P. Vichinsky E, et al. Among authors: harmatz p. Am J Hematol. 2005 Sep;80(1):70-4. doi: 10.1002/ajh.20402. Am J Hematol. 2005. PMID: 16138345 Free article.

2

Variability in hepatic iron concentration in percutaneous needle biopsy specimens from patients with transfusional hemosiderosis.

Butensky E, Fischer R, Hudes M, Schumacher L, Williams R, Moyer TP, Vichinsky E, Harmatz P. Butensky E, et al. Among authors: harmatz p. Am J Clin Pathol. 2005 Jan;123(1):146-52. doi: 10.1309/puuxegxdlh26nxa2. Am J Clin Pathol. 2005. PMID: 15762291

3

Treatment of hepatitis C virus infection in thalassemia.

Butensky E, Pakbaz Z, Foote D, Walters MC, Vichinsky EP, Harmatz P. Butensky E, et al. Among authors: harmatz p. Ann N Y Acad Sci. 2005;1054:290-9. doi: 10.1196/annals.1345.038. Ann N Y Acad Sci. 2005. PMID: 16339677

4

Oxidative stress and inflammation in iron-overloaded patients with beta-thalassaemia or sickle cell disease.

Walter PB, Fung EB, Killilea DW, Jiang Q, Hudes M, Madden J, Porter J, Evans P, Vichinsky E, Harmatz P. Walter PB, et al. Among authors: harmatz p. Br J Haematol. 2006 Oct;135(2):254-63. doi: 10.1111/j.1365-2141.2006.06277.x. Br J Haematol. 2006. PMID: 17010049 Free PMC article.

5

Morbidity and mortality in chronically transfused subjects with thalassemia and sickle cell disease: A report from the multi-center study of iron overload.

Fung EB, Harmatz P, Milet M, Ballas SK, De Castro L, Hagar W, Owen W, Olivieri N, Smith-Whitley K, Darbari D, Wang W, Vichinsky E; Multi-Center Study of Iron Overload Research Group. Fung EB, et al. Among authors: harmatz p. Am J Hematol. 2007 Apr;82(4):255-65. doi: 10.1002/ajh.20809. Am J Hematol. 2007. PMID: 17094096 Free article.

6

Serum ferritin underestimates liver iron concentration in transfusion independent thalassemia patients as compared to regularly transfused thalassemia and sickle cell patients.

Pakbaz Z, Fischer R, Fung E, Nielsen P, Harmatz P, Vichinsky E. Pakbaz Z, et al. Among authors: harmatz p. Pediatr Blood Cancer. 2007 Sep;49(3):329-32. doi: 10.1002/pbc.21275. Pediatr Blood Cancer. 2007. PMID: 17554789

7

Iron homeostasis during transfusional iron overload in beta-thalassemia and sickle cell disease: changes in iron regulatory protein, hepcidin, and ferritin expression.

Jenkins ZA, Hagar W, Bowlus CL, Johansson HE, Harmatz P, Vichinsky EP, Theil EC. Jenkins ZA, et al. Among authors: harmatz p. Pediatr Hematol Oncol. 2007 Jun;24(4):237-43. doi: 10.1080/08880010701360700. Pediatr Hematol Oncol. 2007. PMID: 17613866

8

Patterns of hepatic iron distribution in patients with chronically transfused thalassemia and sickle cell disease.

Ghugre NR, Gonzalez-Gomez I, Butensky E, Noetzli L, Fischer R, Williams R, Harmatz P, Coates TD, Wood JC. Ghugre NR, et al. Among authors: harmatz p. Am J Hematol. 2009 Aug;84(8):480-3. doi: 10.1002/ajh.21456. Am J Hematol. 2009. PMID: 19536851 Free PMC article.

9

Potential mechanisms for altered iron metabolism in human immunodeficiency virus disease.

Butensky E, Kennedy CM, Lee MM, Harmatz P, Miaskowski C. Butensky E, et al. Among authors: harmatz p. J Assoc Nurses AIDS Care. 2004 Nov-Dec;15(6):31-45. doi: 10.1177/1055329004271125. J Assoc Nurses AIDS Care. 2004. PMID: 15538015 Review.

10

A simple model to assess and improve adherence to iron chelation therapy with deferoxamine in patients with thalassemia.

Pakbaz Z, Fischer R, Treadwell M, Yamashita R, Fung EB, Calvelli L, Quirolo K, Foote D, Harmatz P, Vichinsky EP. Pakbaz Z, et al. Among authors: harmatz p. Ann N Y Acad Sci. 2005;1054:486-91. doi: 10.1196/annals.1345.065. Ann N Y Acad Sci. 2005. PMID: 16339703 Clinical Trial.

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