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Showing 10 out of a total of 20 results for community: Faculty of Medicine (FM).
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Deferasirox demonstrates a dose-dependent reduction in liver iron concentration and consistent efficacy across subgroups of non-transfusion-dependent thalassemia patients
Taher A.T.
;
Porter J.B.
;
Viprakasit V.
;
Kattamis A.
;
Chuncharunee S.
;
Sutcharitchan P.
;
Siritanaratkul N.
;
Galanello R.
;
Karakas Z.
;
Lawniczek T.
;
Habr D.
;
Ros J.
;
Zhang Y.
;
Cappellini M.D.
(
HOBOKEN
,
2013
)
Evaluation of the 5mg-g liver iron concentration threshold and its association with morbidity in patients with β-thalassemia intermedia
Musallam K.M.
;
Cappellini M.D.
;
Taher A.T.
(
SAN DIEGO
,
2013
)
Continued improvement in myocardial T2* over two years of deferasirox therapy in β-thalassemia major patients with cardiac iron overload
Pennell D.J.
;
Porter J.B.
;
Cappellini M.D.
;
Chan L.L.
;
El-Beshlawy A.
;
Aydinok Y.
;
Ibrahim H.
;
Li C.-K.
;
Viprakasit V.
;
Elalfy M.S.
;
Kattamis A.
;
Smith G.
;
Habr D.
;
Domokos G.
;
Roubert B.
;
Taher A.
(
PAVIA
,
2011
)
Nontransferrin-bound iron in transfused patients with sickle cell disease
Inati A.
;
Musallam K.M.
;
Cappellini M.D.
;
Duca L.
;
Taher A.T.
(
MALDEN
,
2011
)
Splenectomy and thrombosis: The case of thalassemia intermedia
Taher A.T.
;
Musallam K.M.
;
Karimi M.
;
El-Beshlawy A.
;
Belhoul K.
;
Daar S.
;
Saned M.
;
Cesaretti C.
;
Cappellini M.D.
(
MALDEN
,
2010
)
Deferasirox reduces iron overload significantly in nontransfusion-dependent thalassemia: 1-Year results from a prospective, randomized, double-blind, placebo-controlled study
Taher A.T.
;
Porter J.
;
Viprakasit V.
;
Kattamis A.
;
Chuncharunee S.
;
Sutcharitchan P.
;
Siritanaratkul N.
;
Galanello R.
;
Karakas Z.
;
Lawniczek T.
;
Ros J.
;
Zhang Y.
;
Habr D.
;
Cappellini M.D.
(
WASHINGTON
,
2012
)
Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?
Graziadei G.
;
Refaldi C.
;
Barcellini W.
;
Cesaretti C.
;
Cassinero E.
;
Musallam K.M.
;
Cappellini M.D.
(
PAVIA
,
2012
)
Elevated liver iron concentration is a marker of increased morbidity in patients with β thalassemia intermedia
Musallam K.M.
;
Cappellini M.D.
;
Wood J.C.
;
Motta I.
;
Graziadei G.
;
Tamim H.
;
Taher A.T.
(
PAVIA
,
2011
)
Age-related complications in treatment-naïve patients with thalassaemia intermedia
Taher A.T.
;
Musallam K.M.
;
El-Beshlawy A.
;
Karimi M.
;
Daar S.
;
Belhoul K.
;
Saned M.-S.
;
Graziadei G.
;
Cappellini M.D.
(
MALDEN
,
2010
)
Levels of growth differentiation factor-15 are high and correlate with clinical severity in transfusion-independent patients with β thalassemia intermedia
Musallam K.M.
;
Taher A.T.
;
Duca L.
;
Cesaretti C.
;
Halawi R.
;
Cappellini M.D.
(
SAN DIEGO
,
2011
)
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