Iron overload in non-transfusion-dependent thalassemia: a clinical perspective (Q38013165)

27 August 2017

Iron overload in non-transfusion-dependent thalassemia: a clinical perspective (English)

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27 August 2017

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27 August 2017

4

Ali T Taher

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27 August 2017

Maria D Cappellini

2

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PubMed ID

22631036

27 August 2017

John C Wood

series ordinal

3

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27 August 2017

1 April 2012

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27 August 2017

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27 August 2017

26 Suppl 1

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27 August 2017

S16-9

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Iron overload in thalassaemia intermedia: reassessment of iron chelation strategies.

27 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Liver iron concentrations and urinary hepcidin in beta-thalassemia

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Optimal management of β thalassaemia intermedia.

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Anemia, ineffective erythropoiesis, and hepcidin: interacting factors in abnormal iron metabolism leading to iron overload in β-thalassemia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

beta-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Iron Loading and Overloading due to Ineffective Erythropoiesis

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Identification of TWSG1 as a second novel erythroid regulator of hepcidin expression in murine and human cells

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Hemoglobin H disease: not necessarily a benign disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Heterogeneity of hemoglobin H disease in childhood

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Hepatocellular carcinoma in the thalassaemia syndromes

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Hepatocellular carcinoma in thalassemia: A critical review

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Magnetic resonance evaluation of hepatic and myocardial iron deposition in transfusion-independent thalassemia intermedia compared to regularly transfused thalassemia major patients

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Absence of cardiac siderosis despite hepatic iron overload in Italian patients with thalassemia intermedia: an MRI T2* study.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Magnetic resonance evaluation of liver and myocardial iron deposition in thalassemia intermedia and b-thalassemia major.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Magnetic resonance imaging in the evaluation of iron overload in patients with beta thalassaemia and sickle cell disease

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Organ-specific hemosiderosis and functional correlation in Chinese patients with thalassemia intermedia and hemoglobin H disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Cardiac iron overload in thalassemic patients: an endomyocardial biopsy study

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Elevated liver iron concentration is a marker of increased morbidity in patients with β thalassemia intermedia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Asymptomatic brain magnetic resonance imaging abnormalities in splenectomized adults with thalassemia intermedia.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Brain positron emission tomography in splenectomized adults with β-thalassemia intermedia: uncovering yet another covert abnormality.

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https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Brain magnetic resonance angiography in splenectomized adults with β-thalassemia intermedia.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Correlation of liver iron concentration determined by R2 magnetic resonance imaging with serum ferritin in patients with thalassemia intermedia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

MRI R2 and R2* mapping accurately estimates hepatic iron concentration in transfusion-dependent thalassemia and sickle cell disease patients

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance.

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Levels of non-transferrin-bound iron as an index of iron overload in patients with thalassaemia intermedia

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

Hereditary hemochromatosis--a new look at an old disease

1 reference

https://api.crossref.org/works/10.1016%2FS0268-960X%2812%2970006-1

7 January 2021

10.1016/S0268-960X(12)70006-1

Identifiers

DOI

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27 August 2017

1 reference

PubMed ID

22631036