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Showing results for Thomas D. ballas
Your search for Thomas D. Balalas retrieved no results
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program.
Klarin D, Verma SS, Judy R, Dikilitas O, Wolford BN, Paranjpe I, Levin MG, Pan C, Tcheandjieu C, Spin JM, Lynch J, Assimes TL, Åldstedt Nyrønning L, Mattsson E, Edwards TL, Denny J, Larson E, Lee MTM, Carrell D, Zhang Y, Jarvik GP, Gharavi AG, Harley J, Mentch F, Pacheco JA, Hakonarson H, Skogholt AH, Thomas L, Gabrielsen ME, Hveem K, Nielsen JB, Zhou W, Fritsche L, Huang J, Natarajan P, Sun YV, DuVall SL, Rader DJ, Cho K, Chang KM, Wilson PWF, O'Donnell CJ, Kathiresan S, Scali ST, Berceli SA, Willer C, Jones GT, Bown MJ, Nadkarni G, Kullo IJ, Ritchie M, Damrauer SM, Tsao PS; Veterans Affairs Million Veteran Program†. Klarin D, et al. Circulation. 2020 Oct 27;142(17):1633-1646. doi: 10.1161/CIRCULATIONAHA.120.047544. Epub 2020 Sep 28. Circulation. 2020. PMID: 32981348 Free PMC article.
Rheological properties of sickle erythrocytes in patients with sickle-cell anemia: The effect of hydroxyurea, fetal hemoglobin, and α-thalassemia.
Ballas SK, Connes P; Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. Ballas SK, et al. Eur J Haematol. 2018 Dec;101(6):798-803. doi: 10.1111/ejh.13173. Epub 2018 Oct 9. Eur J Haematol. 2018. PMID: 30204261 Free PMC article.
METHODS: Adult patients were enrolled in the Sickle Cell Program of the Cardeza Foundation (Thomas Jefferson University) and were followed up prospectively during the period in which the Multicenter Study of Hydroxyurea (MSH) in patients with SCA was conducted. ...
METHODS: Adult patients were enrolled in the Sickle Cell Program of the Cardeza Foundation (Thomas Jefferson University) and were fol …
Deferasirox in patients with iron overload secondary to hereditary hemochromatosis: results of a 1-yr Phase 2 study.
Cançado R, Melo MR, de Moraes Bastos R, Santos PC, Guerra-Shinohara EM, Chiattone C, Ballas SK. Cançado R, et al. Eur J Haematol. 2015 Dec;95(6):545-50. doi: 10.1111/ejh.12530. Epub 2015 Mar 27. Eur J Haematol. 2015. PMID: 25684349 Clinical Trial.
This open-label, prospective, phase 2 study evaluated the safety and efficacy of deferasirox (10 5 mg/kg/d) in patients with hereditary hemochromatosis (HH) and iron overload refractory to or intolerant of phlebotomy. ...
This open-label, prospective, phase 2 study evaluated the safety and efficacy of deferasirox (10 5 mg/kg/d) in patients with heredita …
Neonatal screening for sickle cell disease in a metropolitan university hospital: efficacy and problems.
Ballas SK, Park D, Wapner RJ. Ballas SK, et al. J Med Screen. 1994 Oct;1(4):229-32. doi: 10.1177/096914139400100409. J Med Screen. 1994. PMID: 8790526
METHOD: 4845 (73.3%) newborn cord blood samples from 6271 infants born in the Thomas Jefferson University Hospital over a two year period were tested for the presence of haemoglobinopathies. ...CONCLUSIONS: A screening programme for newborns in a metropolitan hospital (a) …
METHOD: 4845 (73.3%) newborn cord blood samples from 6271 infants born in the Thomas Jefferson University Hospital over a two year pe …