A complicated disease: what can be done to manage thalassemia major more effectively? - Wikidata - wikimedia - TriplyDB

A complicated disease: what can be done to manage thalassemia major more effectively?

A complicated disease: what can be done to manage thalassemia major more effectively?

http://www.wikidata.org/entity/Q38607875

about

Cardiac complications in thalassemia major.Laboratory diagnosis of thalassemia.Pregnancy in patients with thalassemia major: a cohort study and conclusions for an adequate care management approach.

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P2860

A complicated disease: what can be done to manage thalassemia major more effectively?

http://www.wikidata.org/entity/Q38607875

description

2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

A complicated disease: what can be done to manage thalassemia major more effectively?

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A complicated disease: what can be done to manage thalassemia major more effectively?

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A complicated disease: what can be done to manage thalassemia major more effectively?

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17474086.2015.1101339

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Expert Review of Hematology

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A complicated disease: what can be done to manage thalassemia major more effectively?

@en

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Caterina Borgna-Pignatti

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Maria Marsella

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Raffaella Origa

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P2860

Psychological therapies for thalassaemia

HLA-matched sibling bone marrow transplantation for β-thalassemia major

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

β-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapies

Bone disease in thalassemia: a frequent and still unresolved problem.

Three-year efficacy, safety, and survival findings from COMFORT-II, a phase 3 study comparing ruxolitinib with best available therapy for myelofibrosis.

Pregnancy and beta-thalassemia: an Italian multicenter experience.

Effects of the anti-receptor activator of nuclear factor kappa B ligand denusomab on beta thalassemia major-induced osteoporosis

Improved clinical outcomes of high risk β thalassemia major patients undergoing a HLA matched related allogeneic stem cell transplant with a treosulfan based conditioning regimen and peripheral blood stem cell grafts

An activin receptor IIA ligand trap promotes erythropoiesis resulting in a rapid induction of red blood cells and haemoglobin

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851-862

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scholarly article

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10.1586/17474086.2015.1101339

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6

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8

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Alessandro Baldan

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282870931

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